首页 > 最新文献

Journal of Cancer Science & Therapy最新文献

英文 中文
Analysis of A Single Para-Aortic Lymph Node Metastasis in Endometrial Cancer 子宫内膜癌单发主动脉旁淋巴结转移的分析
Pub Date : 2018-02-14 DOI: 10.4172/1948-5956.1000510
M. Matsuura, Akimasa Takahashi, H. Nomura, M. Matoda, S. Okamoto, H. Kanao, K. Omatsu, Kazuyoshi Kato, K. Utsugi, N. Takeshima
Objective: To determine the indication for lymph node dissection in patients with endometrial cancer, we investigated the incidence and distribution of single metastatic lymph nodes in patients who underwent systematic pelvic and para-aortic lymph node dissection.Methods: This study involved 910 patients with endometrial cancer who were treated at the Cancer Institute Hospital, Japan, between January 1994 and December 2015. All patients underwent an open hysterectomy with bilateral salpingo-oophorectomy and pelvic and para-aortic lymph nodes dissection.Results: Lymph node metastasis was observed in 199 patients (21.9%), 45 (5%) of whom had single lymph node metastasis. Single lymph node metastasis accounted for 22.6% of all metastatic cases. Myometrial invasion >50% was observed in 30 patients, whereas 15 patients had <50% myometrial invasion. When mapping single lymph node metastatic sites, the para-aortic area had a frequency of 31.1% (14 cases). The distribution of single metastatic lymph nodes spanned a wide area between the pelvic and para-aortic regions. Considering single metastatic nodes and myometrial invasion, 8 patients (53.3%) who had myometrial invasion <50% had a single metastatic node in the para-aortic region. Four of 9 patients (45%) considered low-risk (endometrioid Grade 1-2, invasion depth <50%, no lymphovascular space invasion) showed metastasis to the para-aortic areas.Conclusion: Single metastatic lymph nodes were widely distributed between the pelvic and para-aortic regions, suggesting that detection of a sentinel lymph node in patients with endometrial cancer could be problematic.
目的:探讨子宫内膜癌患者行盆腔及主动脉旁淋巴结清扫术中单个转移性淋巴结的发生率和分布,以确定淋巴结清扫术的适应证。方法:本研究纳入1994年1月至2015年12月在日本癌症研究所医院接受治疗的910例子宫内膜癌患者。所有患者均行开放式子宫切除术、双侧输卵管-卵巢切除术、盆腔及主动脉旁淋巴结清扫术。结果:199例(21.9%)患者出现淋巴结转移,其中45例(5%)为单淋巴结转移。单淋巴结转移占所有转移病例的22.6%。30例患者子宫肌层浸润>50%,15例患者子宫肌层浸润<50%。当绘制单个淋巴结转移部位时,主动脉旁区域的频率为31.1%(14例)。单个转移性淋巴结的分布横跨骨盆和主动脉旁区域之间的广阔区域。考虑到单个转移淋巴结和子宫肌层浸润,子宫肌层浸润<50%的患者中有8例(53.3%)在主动脉旁区有单个转移淋巴结。9例患者中有4例(45%)为低危(子宫内膜样1-2级,浸润深度<50%,无淋巴血管间隙浸润)显示转移至主动脉旁区。结论:单个转移淋巴结广泛分布于盆腔和主动脉旁区,提示子宫内膜癌患者前哨淋巴结的检测可能存在问题。
{"title":"Analysis of A Single Para-Aortic Lymph Node Metastasis in Endometrial Cancer","authors":"M. Matsuura, Akimasa Takahashi, H. Nomura, M. Matoda, S. Okamoto, H. Kanao, K. Omatsu, Kazuyoshi Kato, K. Utsugi, N. Takeshima","doi":"10.4172/1948-5956.1000510","DOIUrl":"https://doi.org/10.4172/1948-5956.1000510","url":null,"abstract":"Objective: To determine the indication for lymph node dissection in patients with endometrial cancer, we investigated the incidence and distribution of single metastatic lymph nodes in patients who underwent systematic pelvic and para-aortic lymph node dissection.Methods: This study involved 910 patients with endometrial cancer who were treated at the Cancer Institute Hospital, Japan, between January 1994 and December 2015. All patients underwent an open hysterectomy with bilateral salpingo-oophorectomy and pelvic and para-aortic lymph nodes dissection.Results: Lymph node metastasis was observed in 199 patients (21.9%), 45 (5%) of whom had single lymph node metastasis. Single lymph node metastasis accounted for 22.6% of all metastatic cases. Myometrial invasion >50% was observed in 30 patients, whereas 15 patients had <50% myometrial invasion. When mapping single lymph node metastatic sites, the para-aortic area had a frequency of 31.1% (14 cases). The distribution of single metastatic lymph nodes spanned a wide area between the pelvic and para-aortic regions. Considering single metastatic nodes and myometrial invasion, 8 patients (53.3%) who had myometrial invasion <50% had a single metastatic node in the para-aortic region. Four of 9 patients (45%) considered low-risk (endometrioid Grade 1-2, invasion depth <50%, no lymphovascular space invasion) showed metastasis to the para-aortic areas.Conclusion: Single metastatic lymph nodes were widely distributed between the pelvic and para-aortic regions, suggesting that detection of a sentinel lymph node in patients with endometrial cancer could be problematic.","PeriodicalId":15170,"journal":{"name":"Journal of Cancer Science & Therapy","volume":"147 1","pages":"1-3"},"PeriodicalIF":0.0,"publicationDate":"2018-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91381539","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Blocking PD1/PDL1 Interactions Together with MLN4924 Therapy is a Potential Strategy for Glioma Treatment. 阻断PD1/PDL1相互作用联合MLN4924治疗是治疗胶质瘤的潜在策略。
Pub Date : 2018-01-01 Epub Date: 2018-08-06 DOI: 10.4172/1948-5956.1000543
Natalia Filippova, Xiuhua Yang, Zixiao An, Louis B Nabors, Larisa Pereboeva

Objective: MLN4924, a pharmacological inhibitor of cullin neddylation, resulted in glioma cell apoptosis, deregulation of the S-phase of DNA synthesis and thus, offers great potential for the treatment of brain tumours. However, targeting the neddylation pathway with an MLN4924 treatment stabilized the hypoxia-inducible factor 1A (HIF1A), which is one of the main transcriptional enhancers of the immune checkpoint molecule PDL1 (programmid death ligand-1) in cancer cells. The influence of immune checkpoint molecules on glioma progression has recently been discovered; PDL1 overexpression in gliomas corresponds to a significant shortening of patient survival and a decrease of the anti-tumour immune response. We hypothesize that i) PDL1 is up-regulated in gliomas after treatment with MLN4924 and induces T-cell energy; ii) co-utilization of the PD1/PDL1 blockage with MLN4924 therapy may reduce T-cell energy and may engage MLN4924-induced tumour disruption with the immune response.

Methods: PDL1 expression and its immunosuppressive role in gliomas, glioma microenvironments, and after treatments with MLN4924 were assessed by utilizing methods of immunohistochemistry, molecular biology, and biochemistry.

Results: We confirmed PDL1 overexpression in clinical brain tumour samples, PDGx and established glioma cell lines, extracellular media from glioma cells, and CSF (cerebrospinal fluid) samples from tumour-bearing mice. Our primary T-cell based assays verified that the up-regulation of PDL1 in tumour cells protects gliomas from T-cell treatment and reduces T-cell activation. We found that a pharmacological inhibitor of cullin neddylation, MLN4924, exhibited strong cytotoxicity towards PDGx and established glioma cell lines, in vitro, with an IC50's range from 0.2 to 3 uM. However, we observed a significant increase of HIF1A and PDL1 in mRNA and protein levels in all glioma cell lines after treatment with MLN4924. The MLN4924-dependent induction of PDL1 in gliomas resulted in T-cell energy, which was blocked by a blockage of the PD1/PDL1 interaction.

Conclusion: We conclude that i) PDL1 up-regulation in gliomas and the glioma microenvironment is an important chemotherapeutic target; ii) MLN4924 therapy, combined with a blockage of the PD1/PDL1 pathway, should be considered as a potential strategy for glioma treatment.

目的:MLN4924是一种抑制cullin类化修饰的药物抑制剂,可导致胶质瘤细胞凋亡,抑制DNA合成的s期,因此在脑肿瘤的治疗中具有很大的潜力。然而,用MLN4924靶向类化修饰通路稳定了低氧诱导因子1A (HIF1A), HIF1A是癌细胞中免疫检查点分子PDL1(程序性死亡配体-1)的主要转录增强子之一。免疫检查点分子对胶质瘤进展的影响最近才被发现;胶质瘤中PDL1的过表达与患者生存期的显著缩短和抗肿瘤免疫反应的降低相对应。我们假设i)在MLN4924治疗后,PDL1在胶质瘤中上调并诱导t细胞能量;ii) PD1/PDL1阻断与MLN4924治疗的共同利用可能降低t细胞能量,并可能参与MLN4924诱导的肿瘤破坏与免疫反应。方法:采用免疫组织化学、分子生物学和生物化学等方法,评价MLN4924在胶质瘤、胶质瘤微环境和治疗后PDL1的表达及其免疫抑制作用。结果:我们证实PDL1在临床脑肿瘤样本、PDGx和已建立的胶质瘤细胞系、胶质瘤细胞的细胞外介质和荷瘤小鼠脑脊液样本中过表达。我们基于原代t细胞的实验证实,肿瘤细胞中PDL1的上调可以保护胶质瘤免受t细胞的治疗,并降低t细胞的活化。我们发现cullin类化修饰的药理学抑制剂MLN4924在体外对PDGx和已建立的胶质瘤细胞系表现出很强的细胞毒性,其IC50范围为0.2至3 uM。然而,我们观察到MLN4924处理后,所有胶质瘤细胞系中HIF1A和PDL1的mRNA和蛋白水平显著增加。在胶质瘤中,依赖mln4924的PDL1诱导导致t细胞能量,这被PD1/PDL1相互作用的阻断所阻断。结论:1)胶质瘤及胶质瘤微环境中PDL1上调是重要的化疗靶点;ii) MLN4924疗法联合阻断PD1/PDL1通路,应被视为治疗胶质瘤的潜在策略。
{"title":"Blocking PD1/PDL1 Interactions Together with MLN4924 Therapy is a Potential Strategy for Glioma Treatment.","authors":"Natalia Filippova,&nbsp;Xiuhua Yang,&nbsp;Zixiao An,&nbsp;Louis B Nabors,&nbsp;Larisa Pereboeva","doi":"10.4172/1948-5956.1000543","DOIUrl":"https://doi.org/10.4172/1948-5956.1000543","url":null,"abstract":"<p><strong>Objective: </strong>MLN4924, a pharmacological inhibitor of cullin neddylation, resulted in glioma cell apoptosis, deregulation of the S-phase of DNA synthesis and thus, offers great potential for the treatment of brain tumours. However, targeting the neddylation pathway with an MLN4924 treatment stabilized the hypoxia-inducible factor 1A (HIF1A), which is one of the main transcriptional enhancers of the immune checkpoint molecule PDL1 (programmid death ligand-1) in cancer cells. The influence of immune checkpoint molecules on glioma progression has recently been discovered; PDL1 overexpression in gliomas corresponds to a significant shortening of patient survival and a decrease of the anti-tumour immune response. We hypothesize that i) PDL1 is up-regulated in gliomas after treatment with MLN4924 and induces T-cell energy; ii) co-utilization of the PD1/PDL1 blockage with MLN4924 therapy may reduce T-cell energy and may engage MLN4924-induced tumour disruption with the immune response.</p><p><strong>Methods: </strong>PDL1 expression and its immunosuppressive role in gliomas, glioma microenvironments, and after treatments with MLN4924 were assessed by utilizing methods of immunohistochemistry, molecular biology, and biochemistry.</p><p><strong>Results: </strong>We confirmed PDL1 overexpression in clinical brain tumour samples, PDGx and established glioma cell lines, extracellular media from glioma cells, and CSF (cerebrospinal fluid) samples from tumour-bearing mice. Our primary T-cell based assays verified that the up-regulation of PDL1 in tumour cells protects gliomas from T-cell treatment and reduces T-cell activation. We found that a pharmacological inhibitor of cullin neddylation, MLN4924, exhibited strong cytotoxicity towards PDGx and established glioma cell lines, <i>in vitro</i>, with an IC50's range from 0.2 to 3 uM. However, we observed a significant increase of HIF1A and PDL1 in mRNA and protein levels in all glioma cell lines after treatment with MLN4924. The MLN4924-dependent induction of PDL1 in gliomas resulted in T-cell energy, which was blocked by a blockage of the PD1/PDL1 interaction.</p><p><strong>Conclusion: </strong>We conclude that i) PDL1 up-regulation in gliomas and the glioma microenvironment is an important chemotherapeutic target; ii) MLN4924 therapy, combined with a blockage of the PD1/PDL1 pathway, should be considered as a potential strategy for glioma treatment.</p>","PeriodicalId":15170,"journal":{"name":"Journal of Cancer Science & Therapy","volume":"10 8","pages":"190-197"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/1948-5956.1000543","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36694216","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 22
The Pretreatment Tumor Infiltrating T Lymphocytes (CD8 + , CD4 + , FOXP3 + ) and Systemic Neutrophil-Lymphocytes Ratio in Definitively Treated Cervical Cancer Patients: The Correlation to Clinicopathological Factors and Survival 宫颈癌根治患者肿瘤浸润T淋巴细胞(CD8 +、CD4 +、FOXP3 +)及全身中性粒细胞/淋巴细胞比值:与临床病理因素及生存率的关系
Pub Date : 2018-01-01 DOI: 10.4172/1948-5956.1000528
Hala A El-Lathy, Ahlam A Dohal, M. Mashhour
Purpose: To evaluate the prognostic potential of pre-treatment tumour infiltrating T lymphocytes (TILs) (CD8+, CD4+, FOXP3+) and systemic neutrophil to lymphocyte ratio (NLR) in predicting the outcome of definitively treated cervical cancer patients.Methods: Both densities of pre-treatment TILs (CD8+, CD4+, FOXP3+) in cervical biopsies and NLR were correlated with clinicopathological parameters. The prognostic value of pre-treatment TILs and NLR for disease free survival (DFS) and overall survival (OS) were assessed using Log rank and Cox regression.Results: The final analysis included 28 had who radical hysterectomy while 20 had definitive concurrent chemoradiation. Elevated CD8+, CD8+/CD4+ and low FOXP3+ were associated with node negative, early stage disease and radical hysterectomies. Conversely, elevated NLR was associated with advanced stages, nodal involvement and definitive chemoradiation. Cox regression multivariate revealed that elevated NLR along with nodal involvement were independently correlated with poor prognosis with hazard ratio (HR 3.06 (95% confidence interval [CI], 3.45-9.24),5.63 (95% CI, 2.61-9.32) for OS and (HR 8.21 (95% CI, 4.21-16.53) and 5.32 (95% CI, 2.37-10.24) for DFS respectively. Additionally, FOXP3+ ≥ 19 and CD8+/CD4+ < 2 were significantly associated with decreased OS (HR 4.37 (95% CI, 2.48-12.37), 2.31 (95% CI, 2.34-9.32) and poorer DFS (HR 3.61 (95% CI, 1.38- 9.32), 4.32 (95% CI,3.12-8.34) respectively.Conclusion: The Pre-treatment NLR, CD8+, FOXP3+ and C8/CD4+ showed a significant association with different clinicopathological prognostic factors in definitively treated cervical cancer patients. Additionally, they may be considered as potential independent prognostic indicators of clinical outcomes.
目的:探讨治疗前肿瘤浸润T淋巴细胞(TILs) (CD8+、CD4+、FOXP3+)和全身中性粒细胞/淋巴细胞比值(NLR)对宫颈癌患者预后的预测价值。方法:术前宫颈活检和NLR中TILs (CD8+、CD4+、FOXP3+)密度与临床病理参数的相关性。采用Log rank和Cox回归评估治疗前TILs和NLR对无病生存期(DFS)和总生存期(OS)的预后价值。结果:28例患者行根治性子宫切除术,20例患者行同步放化疗。CD8+、CD8+/CD4+升高和FOXP3+低与淋巴结阴性、早期疾病和根治性子宫切除术相关。相反,NLR升高与晚期、淋巴结受累和最终放化疗有关。多因素Cox回归分析显示,NLR升高伴淋巴结受累与预后不良独立相关,风险比OS为3.06(95%可信区间[CI], 3.45-9.24)、5.63 (95% CI, 2.61-9.32), DFS为8.21 (95% CI, 4.21-16.53)、5.32 (95% CI, 2.37-10.24)。此外,FOXP3+≥19和CD8+/CD4+ < 2与OS降低(HR 4.37 (95% CI, 2.48-12.37)、2.31 (95% CI, 2.34-9.32)和DFS降低(HR 3.61 (95% CI, 1.38- 9.32)、4.32 (95% CI,3.12-8.34)显著相关。结论:宫颈癌患者治疗前NLR、CD8+、FOXP3+、C8/CD4+与不同临床病理预后因素有显著相关性。此外,它们可能被认为是临床结果的潜在独立预后指标。
{"title":"The Pretreatment Tumor Infiltrating T Lymphocytes (CD8 + , CD4 + , FOXP3 + ) and Systemic Neutrophil-Lymphocytes Ratio in Definitively Treated Cervical Cancer Patients: The Correlation to Clinicopathological Factors and Survival","authors":"Hala A El-Lathy, Ahlam A Dohal, M. Mashhour","doi":"10.4172/1948-5956.1000528","DOIUrl":"https://doi.org/10.4172/1948-5956.1000528","url":null,"abstract":"Purpose: To evaluate the prognostic potential of pre-treatment tumour infiltrating T lymphocytes (TILs) (CD8+, CD4+, FOXP3+) and systemic neutrophil to lymphocyte ratio (NLR) in predicting the outcome of definitively treated cervical cancer patients.Methods: Both densities of pre-treatment TILs (CD8+, CD4+, FOXP3+) in cervical biopsies and NLR were correlated with clinicopathological parameters. The prognostic value of pre-treatment TILs and NLR for disease free survival (DFS) and overall survival (OS) were assessed using Log rank and Cox regression.Results: The final analysis included 28 had who radical hysterectomy while 20 had definitive concurrent chemoradiation. Elevated CD8+, CD8+/CD4+ and low FOXP3+ were associated with node negative, early stage disease and radical hysterectomies. Conversely, elevated NLR was associated with advanced stages, nodal involvement and definitive chemoradiation. Cox regression multivariate revealed that elevated NLR along with nodal involvement were independently correlated with poor prognosis with hazard ratio (HR 3.06 (95% confidence interval [CI], 3.45-9.24),5.63 (95% CI, 2.61-9.32) for OS and (HR 8.21 (95% CI, 4.21-16.53) and 5.32 (95% CI, 2.37-10.24) for DFS respectively. Additionally, FOXP3+ ≥ 19 and CD8+/CD4+ < 2 were significantly associated with decreased OS (HR 4.37 (95% CI, 2.48-12.37), 2.31 (95% CI, 2.34-9.32) and poorer DFS (HR 3.61 (95% CI, 1.38- 9.32), 4.32 (95% CI,3.12-8.34) respectively.Conclusion: The Pre-treatment NLR, CD8+, FOXP3+ and C8/CD4+ showed a significant association with different clinicopathological prognostic factors in definitively treated cervical cancer patients. Additionally, they may be considered as potential independent prognostic indicators of clinical outcomes.","PeriodicalId":15170,"journal":{"name":"Journal of Cancer Science & Therapy","volume":"1 1","pages":"1-113"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75232795","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mitochondrial Dysfunction in Cross-resistance of Clinically Relevant Radioresistant Cells to X-rays and Docetaxe 临床相关放射耐药细胞对x射线和docetax交叉耐药的线粒体功能障碍
Pub Date : 2018-01-01 DOI: 10.4172/1948-5956.1000571
Yoshikazu Kuwaharaa, K. Tomita, Shintaro Takahashi, Yusuke Urushihara, Yohei Saito, Mehryar Habibi Roudkenar, A. Roushandeh, Tomoaki Sato, A. Kurimasa, M. Fukumoto
{"title":"Mitochondrial Dysfunction in Cross-resistance of Clinically Relevant Radioresistant Cells to X-rays and Docetaxe","authors":"Yoshikazu Kuwaharaa, K. Tomita, Shintaro Takahashi, Yusuke Urushihara, Yohei Saito, Mehryar Habibi Roudkenar, A. Roushandeh, Tomoaki Sato, A. Kurimasa, M. Fukumoto","doi":"10.4172/1948-5956.1000571","DOIUrl":"https://doi.org/10.4172/1948-5956.1000571","url":null,"abstract":"","PeriodicalId":15170,"journal":{"name":"Journal of Cancer Science & Therapy","volume":"18 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73956460","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sequential Double Bridging to Transplant with Diversified Anti- PD1 Monoclonal Antibodies Retreatment in Relapsed Hodgkin Lymphoma: A Case Report 序贯双桥移植与多样化抗PD1单克隆抗体再治疗复发霍奇金淋巴瘤一例报告
Pub Date : 2018-01-01 DOI: 10.4172/1948-5956.1000534
C. Pellegrini, B. Casadei, C. Cellini, L. Argnani, M. Cavo, P. Zinzani
Background: Nivolumab and pembrolizumab are the first two US FDA-approved monoclonal antibodies targeting PD-1 for Hodgkin lymphoma (HL) and provide promising results in the relapsed/refractory setting (HL patients relapsing after autologous stem cell transplantation [ASCT], or with chemorefractory disease and/ or ineligible for ASCT). An interesting area of ongoing research is the possibility of combining different immune checkpoint inhibitors given concomitantly or sequentially in the attempt to maximize the patient responsiveness. Case report: A heavily pre-treated young woman affected by HL, after several attempts, obtained a complete response after ASCT thanks to the bridge with pembrolizumab. After relapse, the patient achieved again a complete response with nivolumab, bridging her to allotransplant. The patient is still in response to a year since the transplant. Discussion and Conclusion: This is the first report which witnesses the safety and the antitumor activity of interchangeable anti-PD1 monoclonal antibodies administered as a retreatment option and as a bridge to allotransplant in a patient who previously got an objective response to another anti-PD1 which brought her to autologous transplant. Retreatment with anti-PD1 monoclonal antibodies could be considered in therapeutic algorithm of relapsed/refractory HL.
背景:Nivolumab和pembrolizumab是美国fda批准的首批两种针对PD-1治疗霍奇金淋巴瘤(HL)的单克隆抗体,在复发/难治性(HL患者在自体干细胞移植(ASCT)后复发,或患有化疗难治性疾病和/或不符合ASCT治疗条件)的情况下提供了有希望的结果。正在进行的一个有趣的研究领域是联合不同的免疫检查点抑制剂同时或依次给予的可能性,以最大限度地提高患者的反应性。病例报告:一名患有HL的年轻女性,经过多次尝试,由于pembrolizumab的桥接治疗,ASCT后获得完全缓解。复发后,患者再次获得完全缓解,将她与同种异体移植连接起来。病人在移植手术一年后仍有反应。讨论和结论:这是第一个报告,见证了可互换的抗pd1单克隆抗体作为再治疗选择和作为异体移植的桥梁,在之前对另一种抗pd1有客观反应的患者中进行自体移植。抗pd1单克隆抗体可作为复发/难治性HL的治疗方案。
{"title":"Sequential Double Bridging to Transplant with Diversified Anti- PD1 Monoclonal Antibodies Retreatment in Relapsed Hodgkin Lymphoma: A Case Report","authors":"C. Pellegrini, B. Casadei, C. Cellini, L. Argnani, M. Cavo, P. Zinzani","doi":"10.4172/1948-5956.1000534","DOIUrl":"https://doi.org/10.4172/1948-5956.1000534","url":null,"abstract":"Background: Nivolumab and pembrolizumab are the first two US FDA-approved monoclonal antibodies targeting PD-1 for Hodgkin lymphoma (HL) and provide promising results in the relapsed/refractory setting (HL patients relapsing after autologous stem cell transplantation [ASCT], or with chemorefractory disease and/ or ineligible for ASCT). An interesting area of ongoing research is the possibility of combining different immune checkpoint inhibitors given concomitantly or sequentially in the attempt to maximize the patient responsiveness. Case report: A heavily pre-treated young woman affected by HL, after several attempts, obtained a complete response after ASCT thanks to the bridge with pembrolizumab. After relapse, the patient achieved again a complete response with nivolumab, bridging her to allotransplant. The patient is still in response to a year since the transplant. Discussion and Conclusion: This is the first report which witnesses the safety and the antitumor activity of interchangeable anti-PD1 monoclonal antibodies administered as a retreatment option and as a bridge to allotransplant in a patient who previously got an objective response to another anti-PD1 which brought her to autologous transplant. Retreatment with anti-PD1 monoclonal antibodies could be considered in therapeutic algorithm of relapsed/refractory HL.","PeriodicalId":15170,"journal":{"name":"Journal of Cancer Science & Therapy","volume":"40 1","pages":"149-151"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85879217","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
The Role of Estrogen Receptors in Proliferation of Non-Small Cell Lung Cancer 雌激素受体在非小细胞肺癌增殖中的作用
Pub Date : 2018-01-01 DOI: 10.4172/1948-5956.1000516
N. Yu, Y. Jia, Yong Yu, L. Deng, Cong Shen, You-min Guo, H. Duan
To explore the expression pattern of ERs in NSCLC tissues and assess their relationship with tumor histopathological variable. In our study, Ers expression was examined using Real-time PCR with specimens of 28 NSCLC patients. It was shown that both ERɑ and Erβ were over expression in NSCLC tissues, and also the Mrna concentration of both ERɑ and Erβ were significantly higher in primary tumor T2 stage than in T1 stage and higher in squamous carcinoma than in adenocarcinoma. However, the activation of ERɑ and Erβ were completely different. To further explore the role of Ers in development and progression of NSCLC, we used Ers selective siRNA or antagonist in vitro experiments. The results showed that Erβ but not ERɑ can mediate E2 induced cell growth, since siRNA targeting Erβ but not ERɑ gene can induce cell cycle arrest at G1 phase by down regulation of cyclinD1 expression, and also cell cycle regulators p21Waf1/Cip1 and p53 were involved in this signaling pathway.
探讨er在非小细胞肺癌组织中的表达规律及其与肿瘤组织病理变量的关系。在我们的研究中,使用Real-time PCR检测了28例NSCLC患者标本中的Ers表达。结果表明,ER]和Erβ在NSCLC组织中均过表达,且ER]和Erβ Mrna浓度在原发性肿瘤T2期显著高于T1期,在鳞状癌中显著高于腺癌。然而,erj和Erβ的活化完全不同。为了进一步探讨Ers在NSCLC发生发展中的作用,我们使用Ers选择性siRNA或拮抗剂进行体外实验。结果表明,Erβ介导E2诱导的细胞生长,Erβ介导的siRNA通过下调cyclinD1的表达诱导细胞周期阻滞在G1期,而eri介导的siRNA介导的eri介导的siRNA介导的细胞周期阻滞在G1期,细胞周期调控因子p21Waf1/Cip1和p53也参与了这一信号通路。
{"title":"The Role of Estrogen Receptors in Proliferation of Non-Small Cell Lung Cancer","authors":"N. Yu, Y. Jia, Yong Yu, L. Deng, Cong Shen, You-min Guo, H. Duan","doi":"10.4172/1948-5956.1000516","DOIUrl":"https://doi.org/10.4172/1948-5956.1000516","url":null,"abstract":"To explore the expression pattern of ERs in NSCLC tissues and assess their relationship with tumor histopathological variable. In our study, Ers expression was examined using Real-time PCR with specimens of 28 NSCLC patients. It was shown that both ERɑ and Erβ were over expression in NSCLC tissues, and also the Mrna concentration of both ERɑ and Erβ were significantly higher in primary tumor T2 stage than in T1 stage and higher in squamous carcinoma than in adenocarcinoma. However, the activation of ERɑ and Erβ were completely different. To further explore the role of Ers in development and progression of NSCLC, we used Ers selective siRNA or antagonist in vitro experiments. The results showed that Erβ but not ERɑ can mediate E2 induced cell growth, since siRNA targeting Erβ but not ERɑ gene can induce cell cycle arrest at G1 phase by down regulation of cyclinD1 expression, and also cell cycle regulators p21Waf1/Cip1 and p53 were involved in this signaling pathway.","PeriodicalId":15170,"journal":{"name":"Journal of Cancer Science & Therapy","volume":"31 1","pages":"45-51"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81646108","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clinical Utility of Poly (ADP-Ribose) Polymerase Inhibitors in Ovarian Cancer 聚adp核糖聚合酶抑制剂在卵巢癌中的临床应用
Pub Date : 2018-01-01 DOI: 10.4172/1948-5956.1000551
Dimple R. Bhatia, Sudeep Gupta
Inhibitors of the enzyme poly (ADP-ribose) polymerase (PARP) are the most promising class of targeted therapies in ovarian cancers in recent times. Approximately 30% to 50% of these cancers are characterized by aberrant DNA repair pathways due to mutations in tumor suppressor genes: BRCA1 or BRCA2. Therapeutic approach with PARP inhibitors in BRCA deficient tumors exploits a synthetic lethal strategy targeting the deficiency in homologous recombination DNA repair pathway. This short review provides an overview of BRCAness in maintaining genomic integrity, the role of PARP in DNA repair, utility of PARP inhibitors as monotherapy or in combination with other therapies, mechanisms of resistance to PARP inhibitors and biomarkers for clinical utility of PARP inhibitors in management of ovarian cancer.
聚(adp -核糖)聚合酶(PARP)抑制剂是近年来卵巢癌最有前途的靶向治疗方法。大约30%至50%的这些癌症的特征是由于肿瘤抑制基因BRCA1或BRCA2突变导致的异常DNA修复途径。PARP抑制剂治疗BRCA缺陷肿瘤的方法利用了一种针对同源重组DNA修复途径缺陷的合成致死策略。这篇简短的综述概述了BRCAness在维持基因组完整性方面的作用,PARP在DNA修复中的作用,PARP抑制剂作为单一疗法或与其他疗法联合使用的效用,对PARP抑制剂的耐药机制以及PARP抑制剂在卵巢癌治疗中的临床应用的生物标志物。
{"title":"Clinical Utility of Poly (ADP-Ribose) Polymerase Inhibitors in Ovarian Cancer","authors":"Dimple R. Bhatia, Sudeep Gupta","doi":"10.4172/1948-5956.1000551","DOIUrl":"https://doi.org/10.4172/1948-5956.1000551","url":null,"abstract":"Inhibitors of the enzyme poly (ADP-ribose) polymerase (PARP) are the most promising class of targeted therapies in ovarian cancers in recent times. Approximately 30% to 50% of these cancers are characterized by aberrant DNA repair pathways due to mutations in tumor suppressor genes: BRCA1 or BRCA2. Therapeutic approach with PARP inhibitors in BRCA deficient tumors exploits a synthetic lethal strategy targeting the deficiency in homologous recombination DNA repair pathway. This short review provides an overview of BRCAness in maintaining genomic integrity, the role of PARP in DNA repair, utility of PARP inhibitors as monotherapy or in combination with other therapies, mechanisms of resistance to PARP inhibitors and biomarkers for clinical utility of PARP inhibitors in management of ovarian cancer.","PeriodicalId":15170,"journal":{"name":"Journal of Cancer Science & Therapy","volume":"10 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81179724","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
High Rate of Glycolysis and Cancer 高糖酵解率与癌症
Pub Date : 2018-01-01 DOI: 10.4172/1948-5956.1000531
K-J Tian
One hundred years ago, abnormal metabolism of cancer cell was regarded as one of the most important pathological features of malignancy. Recently, with the development of system biology, researchers regained the interest in regulating cancer metabolism. In 1920s’, Dr. Otto Warburg discovered that, even when oxygen is ample, malignant cells still prefer the anaerobic glycolysis, and the rate of glucose uptake is high while the overall glycolysis increases. Cancer cells divide faster than normal cells, hence they need more bioenergy, and they need to change their metabolism to produce the extra energy. In recent 20 years, the link between high rate of glycolysis and cancer was re-evaluated and has inspired enthusiasm upon research into the metabolism of cancer cells. Novel diagnostic methods and new drugs were created by the understanding of the features of cancer metabolism. Glycolysis in cancer cells has clinical implications in cancer diagnosis, treatment and prognosis. The purpose of this review is to focus on the mechanism of high rate of glycolysis in cancer and its significance in cancer diagnosis and therapies. The regulatory network of cancer is complex, system biology might help us to find the clue. There are evidences showing that mixture of drugs has therapeutic advantages in clinical practice. Combinations of anti-neoplasm drugs have already been administered with encouraging results. Therefore, the multi-targeted MCA advised therapy might be the most promising strategy for cancer. The study for novel inhibitors from medicinal herbs are now ongoing. We believe, there will be more and more therapeutic strategies coming in the near future to help human beings fighting with cancer.
一百年前,癌细胞代谢异常被认为是恶性肿瘤最重要的病理特征之一。近年来,随着系统生物学的发展,研究人员对调节肿瘤代谢重新产生了兴趣。在20世纪20年代,Otto Warburg博士发现,即使在氧气充足的情况下,恶性细胞仍然倾向于厌氧糖酵解,并且糖酵解的整体增加,葡萄糖的摄取率也很高。癌细胞比正常细胞分裂得快,因此它们需要更多的生物能量,它们需要改变自己的新陈代谢来产生额外的能量。近20年来,高糖酵解率与癌症之间的关系被重新评估,激发了对癌细胞代谢研究的热情。对肿瘤代谢特征的认识,创造了新的诊断方法和新药。肿瘤细胞糖酵解对肿瘤的诊断、治疗和预后具有重要的临床意义。本文就糖酵解在肿瘤中的高速率机制及其在肿瘤诊断和治疗中的意义进行综述。癌症的调控网络是复杂的,系统生物学可能会帮助我们找到线索。在临床实践中,有证据表明混合用药具有治疗优势。联合使用抗肿瘤药物已经取得了令人鼓舞的结果。因此,多靶点MCA建议治疗可能是最有希望的癌症治疗策略。从草药中提取新型抑制剂的研究正在进行中。我们相信,在不久的将来会有越来越多的治疗策略来帮助人类与癌症作斗争。
{"title":"High Rate of Glycolysis and Cancer","authors":"K-J Tian","doi":"10.4172/1948-5956.1000531","DOIUrl":"https://doi.org/10.4172/1948-5956.1000531","url":null,"abstract":"One hundred years ago, abnormal metabolism of cancer cell was regarded as one of the most important pathological features of malignancy. Recently, with the development of system biology, researchers regained the interest in regulating cancer metabolism. In 1920s’, Dr. Otto Warburg discovered that, even when oxygen is ample, malignant cells still prefer the anaerobic glycolysis, and the rate of glucose uptake is high while the overall glycolysis increases. Cancer cells divide faster than normal cells, hence they need more bioenergy, and they need to change their metabolism to produce the extra energy. In recent 20 years, the link between high rate of glycolysis and cancer was re-evaluated and has inspired enthusiasm upon research into the metabolism of cancer cells. Novel diagnostic methods and new drugs were created by the understanding of the features of cancer metabolism. Glycolysis in cancer cells has clinical implications in cancer diagnosis, treatment and prognosis. The purpose of this review is to focus on the mechanism of high rate of glycolysis in cancer and its significance in cancer diagnosis and therapies. The regulatory network of cancer is complex, system biology might help us to find the clue. There are evidences showing that mixture of drugs has therapeutic advantages in clinical practice. Combinations of anti-neoplasm drugs have already been administered with encouraging results. Therefore, the multi-targeted MCA advised therapy might be the most promising strategy for cancer. The study for novel inhibitors from medicinal herbs are now ongoing. We believe, there will be more and more therapeutic strategies coming in the near future to help human beings fighting with cancer.","PeriodicalId":15170,"journal":{"name":"Journal of Cancer Science & Therapy","volume":"31 1","pages":"140-142"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91018945","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comparative Analysis of Cilengitide with a Novel Integrin Antagonist AV-38/398 in 2D/3D Melanoma Cultures 西伦吉肽与新型整合素拮抗剂AV-38/398在2D/3D黑色素瘤培养中的比较分析
Pub Date : 2018-01-01 DOI: 10.4172/1948-5956.1000561
E. Selzer
{"title":"Comparative Analysis of Cilengitide with a Novel Integrin Antagonist AV-38/398 in 2D/3D Melanoma Cultures","authors":"E. Selzer","doi":"10.4172/1948-5956.1000561","DOIUrl":"https://doi.org/10.4172/1948-5956.1000561","url":null,"abstract":"","PeriodicalId":15170,"journal":{"name":"Journal of Cancer Science & Therapy","volume":"27 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90209208","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Prophetic Chemo Is the Safest, Cheapest and Most Effective Alternative to Modern Chemotherapy for the Cure of all Forms of Cancers – A Review 预言化疗是最安全,最便宜和最有效的替代现代化疗治疗所有形式的癌症-综述
Pub Date : 2018-01-01 DOI: 10.4172/1948-5956.1000525
H. Deena, M. Hussain
Like all other great Prophets (as) of Allah (God), statements of the Prophet (peace be upon him) of Islam are divinely inspired. Prophet Muhammad (PBUH) never spoke a single lie in his lifetime. Whatever he spoke was under divine inspiration. Concerning his statements and utterances Allah says in the Qur'an: “He does not speak anything on his own. It is but a Revelation which is sent down to him” (An-Najm 53:3-4). “And if Muhammad had made up about Us some [false] sayings, we would have seized him by the right hand; then We would have cut from him the aorta” (Al-Haqqah, 69: 44-46). So, traditions of the Prophet (PBUH) on healing are also true, which modern science proves through research after 14 centuries. Although the Prophet’s mission was neither as a physician or pharmacist, he was inspired by God to make nearly 1000 statements on healing for the benefit of humankind because man needs to remain well free from sickness to fulfill his brief mission on earth. About Nigella sativa Abu Hurayrah (ra) narrates that the Prophet (PBUH) said: "Hold on (use this seed regularly)! Because it is a remedy (cure) for every disease except death." (Bukhari, Muslim) This amazing statement of the Prophet (PBUH) generated tremendous interest among the world scientific community, which finally led them to carry out extensive biological and phytochemical investigations on the plant seed. However, the researchers after carrying out hundreds of studies in various countries finally concluded that black seed can effectively cure 129 different types of ailments including 17 types of cancers. This large number of diseases curable by black seed demonstrates the authenticity of the Prophet’s statement. In this paper the learned readers will be informed about the beneficial pharmacological effects of Nigella sativa in the treatment of most human ailments as well as the findings of modern scientific researches on how Prophetic chemo isolated from Nigella sativa can effectively cure numerous cancers without any side effects.
像安拉(真主)的所有其他伟大的先知一样,伊斯兰教的先知(愿主福安之)的言论是神圣的启示。先知穆罕默德(愿主福安之)一生中从未说过一句谎话。他所说的一切都是神的启示。关于他的言论,真主在《古兰经》中说:“他不凭自己说什么。这不过是降给他的一个启示”(anjam 53:3-4)。“假若穆罕默德为我们捏造假话,我们必定抓住他的右手;然后我们就会切断他的主动脉”(Al-Haqqah, 69: 44-46)。因此,先知(PBUH)关于治疗的传统也是正确的,现代科学通过14世纪后的研究证明了这一点。虽然先知的使命既不是医生也不是药剂师,但他受上帝的启发,为了人类的利益发表了近1000条关于治疗的声明,因为人类需要保持健康,远离疾病,以完成他在地球上的短暂使命。Abu Hurayrah (ra)叙述说,先知(愿主福安之)说:“坚持(经常使用这种种子)!因为它是除死亡以外的所有疾病的良药。”(布哈里,穆斯林)先知(愿主福安之)这一惊人的声明引起了世界科学界的极大兴趣,最终导致他们对植物种子进行了广泛的生物学和植物化学研究。然而,研究人员在各国进行了数百项研究后,最终得出结论,黑籽可以有效治疗129种不同类型的疾病,包括17种癌症。大量的疾病可以用黑籽治愈,这证明了先知预言的真实性。在这篇论文中,有知识的读者将被告知黑草在治疗大多数人类疾病中的有益药理作用,以及现代科学研究的发现,即从黑草中分离的先知化学如何有效地治愈许多癌症而没有任何副作用。
{"title":"Prophetic Chemo Is the Safest, Cheapest and Most Effective Alternative to Modern Chemotherapy for the Cure of all Forms of Cancers – A Review","authors":"H. Deena, M. Hussain","doi":"10.4172/1948-5956.1000525","DOIUrl":"https://doi.org/10.4172/1948-5956.1000525","url":null,"abstract":"Like all other great Prophets (as) of Allah (God), statements of the Prophet (peace be upon him) of Islam are divinely inspired. Prophet Muhammad (PBUH) never spoke a single lie in his lifetime. Whatever he spoke was under divine inspiration. Concerning his statements and utterances Allah says in the Qur'an: “He does not speak anything on his own. It is but a Revelation which is sent down to him” (An-Najm 53:3-4). “And if Muhammad had made up about Us some [false] sayings, we would have seized him by the right hand; then We would have cut from him the aorta” (Al-Haqqah, 69: 44-46). So, traditions of the Prophet (PBUH) on healing are also true, which modern science proves through research after 14 centuries. Although the Prophet’s mission was neither as a physician or pharmacist, he was inspired by God to make nearly 1000 statements on healing for the benefit of humankind because man needs to remain well free from sickness to fulfill his brief mission on earth. About Nigella sativa Abu Hurayrah (ra) narrates that the Prophet (PBUH) said: \"Hold on (use this seed regularly)! Because it is a remedy (cure) for every disease except death.\" (Bukhari, Muslim) This amazing statement of the Prophet (PBUH) generated tremendous interest among the world scientific community, which finally led them to carry out extensive biological and phytochemical investigations on the plant seed. However, the researchers after carrying out hundreds of studies in various countries finally concluded that black seed can effectively cure 129 different types of ailments including 17 types of cancers. This large number of diseases curable by black seed demonstrates the authenticity of the Prophet’s statement. In this paper the learned readers will be informed about the beneficial pharmacological effects of Nigella sativa in the treatment of most human ailments as well as the findings of modern scientific researches on how Prophetic chemo isolated from Nigella sativa can effectively cure numerous cancers without any side effects.","PeriodicalId":15170,"journal":{"name":"Journal of Cancer Science & Therapy","volume":"52 1","pages":"1-14"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73664719","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
期刊
Journal of Cancer Science & Therapy
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1