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Real‑world study of Cerviron® vaginal ovules in the treatment of cervical lesions of various etiologies. Cerviron®阴道胚珠治疗各种病因的宫颈病变的真实世界研究。
IF 2.3 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2023-08-01 DOI: 10.3892/br.2023.1618
Izabella Petre, Daniela Teodora Sirbu, Ramona Petrita, Andreea-Denisa Toma, Ema Peta, Florentina Dimcevici-Poesina

Cervical lesions can be caused by pathogens, hormonal changes or by cervical injury. The recommended treatment in all cases is excision. Local re-epithelialization therapy should be initiated preoperatively and postoperatively. The present study assessed the post-market performance and tolerability of Cerviron® ovules in the treatment and management of cervical lesions postoperatively. The study population included 345 participants aged 20-70 years with either a cervical lesion under treatment or with recent surgical removal of a cervical lesion. The degree of re-epithelialization of the cervical mucosa was improved in 73.17% of the patients evaluated during routine colposcopy exams and 92.73% of patients recorded no bleeding. When adding Cerviron® either as monotherapy or in association with other antimicrobials in postoperative care of the cervical ectropion, improved postoperative outcomes such as reduced post-interventional bleeding and a superior quality of healing were observed. The study and its details are registered in www.clinicaltrials.gov under ID NCT05668806.

宫颈病变可由病原体、激素变化或宫颈损伤引起。所有病例推荐的治疗方法都是切除。局部再上皮化治疗应在术前和术后开始。本研究评估了Cerviron®胚珠在宫颈术后病变治疗和管理中的上市后表现和耐受性。研究人群包括345名年龄在20-70岁之间的参与者,他们要么正在接受宫颈病变治疗,要么最近手术切除了宫颈病变。73.17%的患者经阴道镜检查后宫颈粘膜上皮化程度有所改善,92.73%的患者无出血。在宫颈外翻的术后护理中添加Cerviron®作为单一治疗或与其他抗菌剂联合使用时,观察到改善的术后结果,如减少介入后出血和优越的愈合质量。该研究及其详细信息注册在www.clinicaltrials.gov, ID为NCT05668806。
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引用次数: 0
Herpesvirus entry mediator as a potential biomarker in breast cancer compared with conventional cytotoxic T‑lymphocyte‑associated antigen 4. 与传统细胞毒性T淋巴细胞相关抗原相比,疱疹病毒进入介质作为乳腺癌的潜在生物标志物
IF 2.3 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2023-08-01 DOI: 10.3892/br.2023.1638
Alia Aldahlawi, Fatemah Basingab, Jehan Alrahimi, Kawther Zaher, Peter Natesan Pushparaj, Mohammed A Hassan, Kaltoom Al-Sakkaf

Breast cancer (BC) is the most common cancer in women worldwide, with 2.3 million cases recorded in 2020. Despite improvements in cancer treatment, patients with BC still succumb to the disease, due to regional and distant metastases when diagnosed at later stages. Several immune checkpoint inhibitors have been approved for BC treatment, based on their expression and role in maintaining immunosurveillance against tumors. The present study aimed to evaluate the expression of 12 immune checkpoints in patients with BC, and assess their role as diagnostic and therapeutic markers. Expression levels were measured using reverse transcription-quantitative polymerase chain reaction. Among the 12 immune markers, herpesvirus entry mediator (HVEM) was found to be significantly upregulated in patients with malignant BC compared to non-malignant controls, with a relative fold change (FC) of 1.46 and P=0.012. A similar finding was observed for cytotoxic T-lymphocyte-associated antigen 4 (CTLA4; FC=1.47 and P=0.035). In addition, receiver operating characteristic curve analysis revealed that HVEM expression allowed significant differentiation between groups, with an area under the curve of 0.74 (P=0.013). Upregulation in both HVEM and CTLA4 was revealed to be significantly associated with the human epidermal growth factor receptor-2 (HER2)-enriched phenotype (FC=3.53, P=0.009 and FC=5.98, P=0.002, respectively), while only HVEM was significantly associated with the triple-negative phenotype (FC=2.07, P=0.016). Furthermore, HVEM was significantly higher in patients with grade III tumors (FC=1.88, P=0.025) and negative vascular invasion (FC=1.67, P=0.046) compared with non-malignant controls. Serum protein levels were assessed by multiplex immunoassay, and a significant increase in HVEM was detected in patients with malignant BC compared with that in non-malignant controls (P=0.035). These data indicated that HVEM may serve as a potential biomarker and target for immunotherapy, especially for certain types of BC.

乳腺癌(BC)是全球女性中最常见的癌症,2020年有230万例病例记录。尽管癌症治疗有所改善,但由于在晚期诊断时出现局部和远处转移,BC患者仍然死于该疾病。几种免疫检查点抑制剂已被批准用于BC治疗,基于它们的表达和在维持对肿瘤的免疫监视中的作用。本研究旨在评估12个免疫检查点在BC患者中的表达,并评估其作为诊断和治疗标志物的作用。用逆转录-定量聚合酶链反应测定表达水平。在12种免疫标记物中,与非恶性对照相比,恶性BC患者中疱疹病毒进入介质(HVEM)显著上调,相对折叠变化(FC)为1.46,P=0.012。细胞毒性t淋巴细胞相关抗原4 (CTLA4;FC=1.47, P=0.035)。此外,受试者工作特征曲线分析显示,HVEM表达在组间存在显著差异,曲线下面积为0.74 (P=0.013)。HVEM和CTLA4的上调与人表皮生长因子受体-2 (HER2)富集表型显著相关(FC=3.53, P=0.009和FC=5.98, P=0.002),而只有HVEM与三阴性表型显著相关(FC=2.07, P=0.016)。此外,III级肿瘤(FC=1.88, P=0.025)和血管浸润阴性(FC=1.67, P=0.046)患者的HVEM明显高于非恶性对照。通过多重免疫分析法评估血清蛋白水平,与非恶性对照相比,恶性BC患者的HVEM显著升高(P=0.035)。这些数据表明,HVEM可能作为一种潜在的生物标志物和免疫治疗靶点,特别是对某些类型的BC。
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引用次数: 0
Disease duration and herpes zoster infection related to neutropenia in patients with systemic lupus erythematosus. 系统性红斑狼疮患者中性粒细胞减少与病程和带状疱疹感染的关系。
IF 2.3 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2023-08-01 DOI: 10.3892/br.2023.1636
Worakan Tipsing, Chutatip Limkunakul, Poonsuk Pichaivejchakul, Kittisak Sawanyawisuth

Systemic lupus erythematosus (SLE) is an autoimmune disease involving several organs. Neutropenia in patients with SLE may be a factor associated with infection leading to higher morbidity and mortality. There are several inconsistent predictors of neutropenia in patients with SLE. The present study is a retrospective, analytical study, which aimed to identify other predictors of neutropenia in patients with SLE. Patients with SLE who had been regularly followed up for ≥1 year were included in this study. Clinical factors, including history of disease, comorbidities, previous infection, laboratory results and treatment, were collected. The primary analyzed indicator was the occurrence of neutropenia. Factors associated with neutropenia were calculated by multivariate logistic regression analysis. A total of 84 patients met the study criteria. Of those 84 patients, 36 (42.86%) developed neutropenia. There were seven factors placed in the predictive model for neutropenia. Two factors were independently associated with the presence of neutropenia: Disease duration and herpes zoster infection. The first factor was negatively related with neutropenia with an adjusted odds ratio of 0.70 (95% confidence interval, 0.54, 0.92), whereas herpes zoster infection was an independent risk factor for neutropenia with an adjusted odds ratio of 8.46 (95% confidence interval, 1.30, 54.80). In conclusion, the present study revealed that short duration of disease and herpes zoster infection are predictors of neutropenia in patients with SLE.

系统性红斑狼疮(SLE)是一种累及多个器官的自身免疫性疾病。SLE患者中性粒细胞减少可能是导致较高发病率和死亡率的感染相关因素。有几个不一致的预测SLE患者中性粒细胞减少的因素。本研究是一项回顾性分析性研究,旨在确定SLE患者中性粒细胞减少的其他预测因素。定期随访≥1年的SLE患者纳入本研究。收集临床因素,包括疾病史、合并症、既往感染、实验室结果和治疗。主要分析指标为中性粒细胞减少的发生情况。通过多元logistic回归分析计算与中性粒细胞减少症相关的因素。共有84例患者符合研究标准。84例患者中,36例(42.86%)发生中性粒细胞减少症。中性粒细胞减少症的预测模型中有7个因素。两个因素与中性粒细胞减少症的存在独立相关:疾病持续时间和带状疱疹感染。第一个因素与中性粒细胞减少负相关,校正比值比为0.70(95%可信区间,0.54,0.92),而带状疱疹感染是中性粒细胞减少的独立危险因素,校正比值比为8.46(95%可信区间,1.30,54.80)。总之,本研究揭示病程短和带状疱疹感染是SLE患者中性粒细胞减少的预测因素。
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引用次数: 0
Evolution of a surgical system using deep learning in minimally invasive surgery (Review). 在微创手术中使用深度学习的手术系统的发展(综述)。
IF 2.3 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2023-07-01 DOI: 10.3892/br.2023.1628
Kenbun Sone, Saki Tanimoto, Yusuke Toyohara, Ayumi Taguchi, Yuichiro Miyamoto, Mayuyo Mori, Takayuki Iriyama, Osamu Wada-Hiraike, Yutaka Osuga

Recently, artificial intelligence (AI) has been applied in various fields due to the development of new learning methods, such as deep learning, and the marked progress in computational processing speed. AI is also being applied in the medical field for medical image recognition and omics analysis of genomes and other data. Recently, AI applications for videos of minimally invasive surgeries have also advanced, and studies on such applications are increasing. In the present review, studies that focused on the following topics were selected: i) Organ and anatomy identification, ii) instrument identification, iii) procedure and surgical phase recognition, iv) surgery-time prediction, v) identification of an appropriate incision line, and vi) surgical education. The development of autonomous surgical robots is also progressing, with the Smart Tissue Autonomous Robot (STAR) and RAVEN systems being the most reported developments. STAR, in particular, is currently being used in laparoscopic imaging to recognize the surgical site from laparoscopic images and is in the process of establishing an automated suturing system, albeit in animal experiments. The present review examined the possibility of fully autonomous surgical robots in the future.

近年来,由于新的学习方法的发展,如深度学习,以及计算处理速度的显著进步,人工智能(AI)已被应用于各个领域。人工智能也被应用于医学领域,用于医学图像识别和基因组组学分析等数据。近年来,人工智能在微创手术视频中的应用也有所进展,相关研究也在不断增加。在本综述中,重点选择了以下主题的研究:i)器官和解剖鉴定,ii)器械鉴定,iii)程序和手术阶段识别,iv)手术时间预测,v)确定合适的切口线,vi)外科教育。自主手术机器人的发展也在取得进展,其中智能组织自主机器人(STAR)和RAVEN系统是报道最多的发展。尤其是STAR,目前正被用于腹腔镜成像,从腹腔镜图像中识别手术部位,并且正在建立一个自动缝合系统,尽管是在动物实验中。本综述探讨了未来全自动手术机器人的可能性。
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引用次数: 2
Ring finger protein 215 is a potential prognostic biomarker involved in immune infiltration and angiogenesis in colorectal cancer. 无名指蛋白215是一种潜在的预后生物标志物,参与结直肠癌的免疫浸润和血管生成。
IF 2.3 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2023-07-01 DOI: 10.3892/br.2023.1633
Jing-Bo Wu, Xiao-Jing Li, Hui Liu, Xiu-Ping Liu

The prognostic value of ring finger protein 215 (RNF215) in colorectal cancer (CRC) is unclear. Herein, the present study aimed to investigate the precise value of RNF215 based on CRC datasets from The Cancer Genome Atlas (TCGA) and clinical cases. CRC patient data was collected from TCGA and clinical samples from the Department of Pathology, Shanghai Fifth People's Hospital, Fudan University (Shanghai, China). Logistic regression analysis was used to investigate the correlations between RNF215 and clinicopathological characteristics. The predictive value of RNF215 for the clinical outcome of CRC was determined using Kaplan-Meier curves and Cox regression. Gene set enrichment analysis (GSEA), single-sample GSEA (ssGSEA), and angiogenesis analysis were also conducted to investigate the biological role of RNF215. Immunohistochemistry was conducted to validate the results. The results of the present study confirmed that RNF215 protein expression was significantly associated with age, lymphatic invasion, and overall survival (OS). Univariate analysis showed that upregulation of RNF215 in CRC was significantly associated with age and lymphatic invasion. Kaplan-Meier survival analysis revealed that high RNF215 expression predicted poorer OS and disease-specific survival. A total of nine experimentally detected RNF215-binding proteins were identified with the STRING tool and Cytoscape software. GSEA suggested that RNF215 was associated with several important pathways involved in tumor occurrence, including the Kyoto Encyclopedia of Genes and Genomes MAPK signaling pathway and the WikiPathway RAS signaling pathway. ssGSEA confirmed that RNF215 was significantly expressed in natural killer cells, CD8 T cells and T helper cells. Angiogenesis analysis revealed that numerous angiogenesis-related genes had the same expression trend as RNF215 in CRC. The immunostaining results indicated that RNF215 expression was significantly higher in CRC tissues than in corresponding normal tissues. In conclusion, increased RNF215 expression may be a potential molecular marker predictive of poor survival and a treatment target in CRC. In addition, RNF215 may participate in the formation of CRC through a variety of signaling pathways.

环指蛋白215 (RNF215)在结直肠癌(CRC)中的预后价值尚不清楚。因此,本研究旨在基于来自癌症基因组图谱(TCGA)的CRC数据集和临床病例来研究RNF215的精确价值。CRC患者数据来自TCGA和复旦大学(中国上海)上海第五人民医院病理科的临床样本。采用Logistic回归分析探讨RNF215与临床病理特征的相关性。采用Kaplan-Meier曲线和Cox回归确定RNF215对结直肠癌临床结局的预测价值。通过基因集富集分析(GSEA)、单样本基因集富集分析(ssGSEA)和血管生成分析来研究RNF215的生物学作用。采用免疫组化方法验证结果。本研究结果证实,RNF215蛋白表达与年龄、淋巴侵袭和总生存期(OS)显著相关。单因素分析显示,CRC中RNF215的上调与年龄和淋巴浸润显著相关。Kaplan-Meier生存分析显示,高RNF215表达预测较差的OS和疾病特异性生存。利用STRING工具和Cytoscape软件共鉴定了9个实验检测到的rnf215结合蛋白。GSEA提示RNF215与参与肿瘤发生的几个重要通路相关,包括京都基因与基因组百科全书MAPK信号通路和WikiPathway RAS信号通路。ssGSEA证实RNF215在自然杀伤细胞、CD8 T细胞和T辅助细胞中显著表达。血管生成分析显示,许多血管生成相关基因在CRC中与RNF215具有相同的表达趋势。免疫染色结果显示,RNF215在结直肠癌组织中的表达明显高于相应的正常组织。综上所述,RNF215表达升高可能是CRC患者生存不良的潜在分子标志物和治疗靶点。此外,RNF215可能通过多种信号通路参与CRC的形成。
{"title":"Ring finger protein 215 is a potential prognostic biomarker involved in immune infiltration and angiogenesis in colorectal cancer.","authors":"Jing-Bo Wu,&nbsp;Xiao-Jing Li,&nbsp;Hui Liu,&nbsp;Xiu-Ping Liu","doi":"10.3892/br.2023.1633","DOIUrl":"https://doi.org/10.3892/br.2023.1633","url":null,"abstract":"<p><p>The prognostic value of ring finger protein 215 (RNF215) in colorectal cancer (CRC) is unclear. Herein, the present study aimed to investigate the precise value of RNF215 based on CRC datasets from The Cancer Genome Atlas (TCGA) and clinical cases. CRC patient data was collected from TCGA and clinical samples from the Department of Pathology, Shanghai Fifth People's Hospital, Fudan University (Shanghai, China). Logistic regression analysis was used to investigate the correlations between RNF215 and clinicopathological characteristics. The predictive value of RNF215 for the clinical outcome of CRC was determined using Kaplan-Meier curves and Cox regression. Gene set enrichment analysis (GSEA), single-sample GSEA (ssGSEA), and angiogenesis analysis were also conducted to investigate the biological role of RNF215. Immunohistochemistry was conducted to validate the results. The results of the present study confirmed that RNF215 protein expression was significantly associated with age, lymphatic invasion, and overall survival (OS). Univariate analysis showed that upregulation of RNF215 in CRC was significantly associated with age and lymphatic invasion. Kaplan-Meier survival analysis revealed that high RNF215 expression predicted poorer OS and disease-specific survival. A total of nine experimentally detected RNF215-binding proteins were identified with the STRING tool and Cytoscape software. GSEA suggested that RNF215 was associated with several important pathways involved in tumor occurrence, including the Kyoto Encyclopedia of Genes and Genomes MAPK signaling pathway and the WikiPathway RAS signaling pathway. ssGSEA confirmed that RNF215 was significantly expressed in natural killer cells, CD8 T cells and T helper cells. Angiogenesis analysis revealed that numerous angiogenesis-related genes had the same expression trend as RNF215 in CRC. The immunostaining results indicated that RNF215 expression was significantly higher in CRC tissues than in corresponding normal tissues. In conclusion, increased RNF215 expression may be a potential molecular marker predictive of poor survival and a treatment target in CRC. In addition, RNF215 may participate in the formation of CRC through a variety of signaling pathways.</p>","PeriodicalId":8863,"journal":{"name":"Biomedical reports","volume":"19 1","pages":"50"},"PeriodicalIF":2.3,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/7d/07/br-19-01-01633.PMC10293879.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10113421","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: 1
Andrographis paniculata methanol extract suppresses the phosphorylation of ETV6‑NTRK3. 穿心莲甲醇提取物抑制ETV6‑NTRK3的磷酸化。
IF 2.3 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2023-07-01 DOI: 10.3892/br.2023.1630
Hoang Thanh Chi, Vo Ngoc Tram, Nguyen Trung Quan, Bui Thi Kim Ly

ETS variant transcription factor 6 (ETV6)-neurotrophic receptor tyrosine kinase 3 (NTRK3) (EN) fusions are typically found in rare diseases, such as primary renal fibrosarcoma (only six cases have been reported), secretory carcinoma of the breast and salivary gland (1 case), and AML (4 cases). Few cases have been reported, and expression of the EN gene fusion requires additional clinical data and fundamental research to be supported. The aim of the present study was to determine the inhibitory effect of Andrographis paniculata methanol extract (MeAP) on EN-related cell lines, IMS-M2 and BaF3/EN, as well as evaluate the mechanism of action. Vero cells were used as control cells. Trypan blue staining and MTT were used to evaluate the inhibitory effect of MeAP on tested cells. Western blotting and immunoprecipitation were used to detect the activation of EN after MeAP treatment. The IC50 values of MeAP were found to be 12.38±0.57 µg/ml (IMS-M2) and 13.06±0.49 µg/ml (BaF3/EN). MeAP was observed to inhibit cell proliferation in a time, dose, and cell density-dependent manner. The IC50 value for MeAP in Vero cells was markedly higher, at 109.97±4.24 (µg/ml), indicating a much less sensitive effect. Furthermore, MeAP treatment inhibited EN phosphorylation and induced apoptosis in these cells. Collectively, the present study demonstrated that MeAP has an oncogenic effect on EN fusion-positive cell lines, in particular.

ETS变异转录因子6 (ETV6)-神经营养受体酪氨酸激酶3 (NTRK3) (EN)融合通常见于罕见疾病,如原发性肾纤维肉瘤(仅报道了6例),乳腺和唾液腺分泌性癌(1例)和AML(4例)。报道的病例很少,EN基因融合的表达需要额外的临床数据和基础研究的支持。本研究旨在研究穿心莲甲醇提取物(MeAP)对EN相关细胞株、IMS-M2和BaF3/EN的抑制作用,并探讨其作用机制。Vero细胞作为对照细胞。台盼蓝染色和MTT法评价MeAP对被试细胞的抑制作用。采用Western blotting和免疫沉淀法检测MeAP处理后EN的活化情况。MeAP的IC50值分别为12.38±0.57µg/ml (IMS-M2)和13.06±0.49µg/ml (BaF3/EN)。MeAP对细胞增殖的抑制呈时间、剂量和细胞密度依赖性。MeAP在Vero细胞中的IC50值明显较高,为109.97±4.24(µg/ml),表明其敏感性低得多。此外,MeAP处理可抑制EN磷酸化并诱导这些细胞凋亡。总的来说,本研究表明MeAP尤其对EN融合阳性细胞系具有致癌作用。
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引用次数: 0
Role of the SARS‑COV2 infection in the evolution of acute pancreatitis (Review). SARS - COV2感染在急性胰腺炎演变中的作用(综述)
IF 2.3 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2023-07-01 DOI: 10.3892/br.2023.1632
Vlad Pădureanu, Daniel Cosmin Caragea, Mirela Marinela Florescu, Ionela Mihaela Vladu, Patricia Mihaela Rădulescu, Dan Nicolae Florescu, Dumitru Rădulescu, Rodica Pădureanu, Ion Cristian Efrem

Acute pancreatitis is characterized as an inflammatory illness that is life-threatening and causes necrosis as well as simple edema when pancreatic enzymes are activated intraglandularly. It is not known whether severe acute respiratory syndrome coronavirus 2 causes acute pancreatitis. Patients with acute pancreatitis who test positive for coronavirus disease 2019 (COVID-19) frequently have biliary or alcoholic causes. It is unclear how common acute pancreatitis is in patients with COVID-19. By contrast with patients without COVID-19, however, COVID-19-positive patients with acute pancreatitis have a higher mortality as well as a higher risk of necrosis and admission to an intensive care unit. The most common cause of mortality in COVID-19-positive individuals with concurrent severe pancreatitis is acute respiratory distress syndrome. The present study discussed research on the link between COVID-19 infection and acute pancreatitis.

急性胰腺炎的特征是一种危及生命的炎症性疾病,当胰腺酶在肠道内被激活时,会导致坏死和单纯水肿。目前尚不清楚严重急性呼吸综合征冠状病毒2是否会引起急性胰腺炎。2019冠状病毒病(COVID-19)检测呈阳性的急性胰腺炎患者通常有胆道或酒精原因。目前尚不清楚COVID-19患者的急性胰腺炎有多常见。然而,与未感染COVID-19的患者相比,COVID-19阳性急性胰腺炎患者的死亡率更高,坏死和入住重症监护病房的风险也更高。covid -19阳性患者并发严重胰腺炎的最常见死亡原因是急性呼吸窘迫综合征。本研究讨论了COVID-19感染与急性胰腺炎之间关系的研究。
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引用次数: 1
Exploring the optimal vaccination strategy against hepatitis B virus in childhood (Review). 探索儿童乙型肝炎病毒的最佳疫苗接种策略(综述)。
IF 2.3 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2023-07-01 DOI: 10.3892/br.2023.1631
Anna Kramvis, Ioannis N Mammas, Demetrios A Spandidos

Vaccination against hepatitis B virus (HBV) remains the most effective strategy against HBV infection in humans. The present review summarized the optimal vaccination strategies against HBV in childhood. The following points are discussed: i) When and how the first HBV vaccines were developed; ii) the dosages, schedules and injection routes that are used for HBV vaccination; iii) the contraindications for HBV vaccination in the general paediatric population; iv) the challenges with the use of multivalent vaccines; v) the long-term immunogenicity and duration of protection against HBV; vi) the use of selective HBV vaccination and the hepatitis B immune globulin strategy in HBV-exposed infants; and vii) the effectiveness of the current HBV vaccination schemes. The present review is based on a Paediatric Virology Study Group (PVSG) webinar performed in the context of the 8th Workshop on Paediatric Virology.

乙型肝炎病毒(HBV)疫苗接种仍然是对抗人类HBV感染的最有效策略。本文综述了儿童时期抗HBV疫苗接种的最佳策略。讨论了以下几点:i)第一批乙肝疫苗是何时以及如何研制的;ii)用于乙肝疫苗接种的剂量、时间表和注射途径;iii)普通儿科人群接种乙肝疫苗的禁忌症;四)使用多价疫苗的挑战;v)对HBV的长期免疫原性和保护持续时间;(六)在HBV暴露婴儿中使用选择性HBV疫苗接种和乙型肝炎免疫球蛋白策略;以及vii)目前乙肝疫苗接种计划的有效性。本综述基于在第八届儿科病毒学研讨会背景下进行的儿科病毒学研究组(PVSG)网络研讨会。
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引用次数: 1
Gemcitabine‑fucoxanthin combination in human pancreatic cancer cells. 吉西他滨-岩藻黄素组合在人胰腺癌细胞中的作用。
IF 2.3 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2023-07-01 DOI: 10.3892/br.2023.1629
Jun Lu, Xiaowu Jenifer Wu, Amira Hassouna, Kelvin Sheng Wang, Yan Li, Tao Feng, Yu Zhao, Minfeng Jin, Baohong Zhang, Tianlei Ying, Jinyao Li, Lufeng Cheng, Johnson Liu, Yue Huang

Gemcitabine is a chemotherapeutic agent for pancreatic cancer treatment. It has also been demonstrated to inhibit human pancreatic cancer cell lines, MIA PaCa-2 and PANC-1. The aim of the present study was to investigate the suppressive effect of fucoxanthin, a marine carotenoid, in combination with gemcitabine on pancreatic cancer cells. MTT assays and cell cycle analysis using flow cytometry were performed to study the mechanism of action. The results revealed that combining a low dose of fucoxanthin with gemcitabine enhanced the cell viability of human embryonic kidney cells, 293, while a high dose of fucoxanthin enhanced the inhibitory effect of gemcitabine on the cell viability of this cell line. In addition, the enhanced effect of fucoxanthin on the inhibitory effect of gemcitabine on PANC-1 cells was significant (P<0.01). Fucoxanthin combined with gemcitabine also exerted significant enhancement of the anti-proliferation effect in MIA PaCa-2 cells in a concentration dependent manner (P<0.05), compared with gemcitabine treatment alone. In conclusion, fucoxanthin improved the cytotoxicity of gemcitabine on human pancreatic cancer cells at concentrations that were not cytotoxic to non-cancer cells. Thus, fucoxanthin has the potential to be used as an adjunct in pancreatic cancer treatment.

吉西他滨是一种用于胰腺癌治疗的化疗药物。它也被证明可以抑制人胰腺癌细胞系MIA PaCa-2和PANC-1。本研究的目的是研究岩藻黄素,一种海洋类胡萝卜素,联合吉西他滨对胰腺癌细胞的抑制作用。通过MTT实验和流式细胞术细胞周期分析来研究其作用机制。结果表明,低剂量岩藻黄素联合吉西他滨可增强人胚胎肾细胞293的细胞活力,而高剂量岩藻黄素可增强吉西他滨对该细胞系细胞活力的抑制作用。岩藻黄素增强了吉西他滨对PANC-1细胞的抑制作用(P
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引用次数: 2
Programmed death‑ligand 1 expression in tumor cells and tumor‑infiltrating lymphocytes are associated with depth of tumor invasion in penile cancer. 程序性死亡配体1在阴茎癌肿瘤细胞和肿瘤浸润淋巴细胞中的表达与肿瘤浸润深度相关。
IF 2.3 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2023-07-01 DOI: 10.3892/br.2023.1627
Sakkarn Sangkhamanon, Natcha Kotano, Wichien Sirithanaphol, Ukrit Rompsaithong, Pakorn Kiatsopit, Aumkhae Sookprasert, Kosin Wirasorn, Prin Twinprai, Piyakarn Watcharenwong, Jarin Chindaprasirt

The present study aimed to demonstrate the proportion of the programmed death-ligand 1 (PD-L1) expression in penile cancer patients and the association with clinicopathological parameters. Formalin-fixed paraffin-embedded specimens were obtained from 43 patients with primary penile squamous cell carcinoma treated at Srinagarind Hospital, Faculty of Medicine, Khon Kaen University, between 2008 and 2018. PD-L1 expression was evaluated by the immunohistochemistry using an SP263 monoclonal antibody. PD-L1 positivity was defined as >25% tumor cell staining or >25% tumor-associated immune cell staining. The correlation between PD-L1 expression and clinicopathological parameters was analyzed. A total of eight of 43 patients (18.6%) were identified as positive for PD-L1 expression in tumor cells and tumor-infiltrating lymphocytes. In the PD-L1 positive group, there was a significant association with pathological T stage (P=0.014) with a higher percentage of PD-L1 positive tumors in T1 stage compared with T2-T4 stage. In this cohort, there was a trend towards longer survival in patients with positive PD-L1 expression (5-year OS: 75% vs. 61.2%, P=0.19). Lymph node involvement and the location of tumor at the shaft of penis were two independent prognostic factors for survival. In conclusion, the PD-L1 expression was detected in 18% of penile cancer patients and high expression of PD-L1 was associated with the early T stage.

本研究旨在证明程序性死亡配体1 (PD-L1)在阴茎癌患者中的表达比例及其与临床病理参数的关系。2008年至2018年,孔庆恩大学医学院斯利那加林德医院43例原发性阴茎鳞状细胞癌患者的标本经福尔马林固定石蜡包埋。用SP263单克隆抗体免疫组化检测PD-L1表达。PD-L1阳性定义为>25%的肿瘤细胞染色或>25%的肿瘤相关免疫细胞染色。分析PD-L1表达与临床病理参数的相关性。43例患者中有8例(18.6%)肿瘤细胞和肿瘤浸润淋巴细胞中PD-L1表达阳性。PD-L1阳性组与病理T分期有显著相关性(P=0.014), T1期PD-L1阳性肿瘤比例高于T2-T4期。在该队列中,PD-L1阳性表达患者的生存期有延长的趋势(5年OS: 75% vs. 61.2%, P=0.19)。淋巴结受累和肿瘤在阴茎轴的位置是两个独立的预后因素。综上所述,在18%的阴茎癌患者中检测到PD-L1的表达,并且PD-L1的高表达与早期T期相关。
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