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Using IgY for diagnosis of respiratory infections: practical application in COVID-19. 利用IgY诊断呼吸道感染:在COVID-19中的实际应用
IF 2.1 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2025-12-01 Epub Date: 2025-08-18 DOI: 10.1080/20565623.2025.2546245
Cícero Matheus Lima Amaral, Valdester Cavalcante Pinto Júnior, Daniel Freire Lima, Hellen Paula Silva da Costa, Danúbio Andrade Bezerra Farias, João Xavier da Silva Neto, Luiz Francisco Wemmenson Gonçalves Moura, Bruno Bezerra da Silva, Ednardo Rodrigues Freitas, Maurício Fraga Van Tilburg, Maria Izabel Florindo Guedes

Aim: The COVID-19 pandemic underscores the need for expanded diagnostic tools to combat respiratory pathogens with pandemic potential, particularly in developing countries. This study aimed to create a Dot Blotting test utilizing IgY antibodies for acute respiratory infection diagnosis, with COVID-19 as the disease model.

Methods: Leghorn chickens were immunized with precipitated SARS-CoV-2 virus, and IgY antibodies were purified via ammonium sulfate precipitation and titrated by ELISA. Dot Blotting detected viral antigens in saliva samples, demonstrating efficacy comparable to ELISA tests.

Results: The IgY antibody was successfully produced and purified, obtaining a titration of 1:16,000. The ability of IgY to detect SARS-CoV-2 in clinical saliva samples showed promising results in terms of accuracy (91.3%), sensitivity (92.5%), specificity (90.0%), positive predictive value (PPV) (90.2%), negative predictive value (NPV) (92.3%), and Cohen's Kappa (0.825).

Conclusion: Chicken antibodies proved effective for early and accurate diagnosis of respiratory infections, including COVID-19. This study validates the efficacy of chicken antibodies in diagnosing respiratory infections, supporting pandemic response in developing nations. Expanding diagnostic capabilities is crucial for combating respiratory pathogens.

目的:2019冠状病毒病大流行突出表明,需要扩大诊断工具,以对抗具有大流行潜力的呼吸道病原体,特别是在发展中国家。本研究旨在以COVID-19为疾病模型,建立一种利用IgY抗体进行急性呼吸道感染诊断的Dot Blotting检测方法。方法:用沉淀的SARS-CoV-2病毒免疫来角鸡,用硫酸铵沉淀法纯化IgY抗体,ELISA法定量。Dot Blotting检测唾液样本中的病毒抗原,显示出与ELISA测试相当的功效。结果:成功制备并纯化了IgY抗体,滴度为1:16 000。IgY检测临床唾液样本中SARS-CoV-2的准确性(91.3%)、敏感性(92.5%)、特异性(90.0%)、阳性预测值(PPV)(90.2%)、阴性预测值(NPV)(92.3%)和Cohen’s Kappa(0.825)均显示出良好的结果。结论:鸡抗体可用于包括COVID-19在内的呼吸道感染的早期准确诊断。这项研究验证了鸡抗体在诊断呼吸道感染方面的功效,为发展中国家的大流行应对提供了支持。扩大诊断能力对于抗击呼吸道病原体至关重要。
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引用次数: 0
Endovascular thrombectomy of acute ischemic stroke patients with systemic lupus erythematosus: two case reports. 急性缺血性脑卒中合并系统性红斑狼疮患者血管内血栓切除术2例报告。
IF 2.4 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2025-12-01 Epub Date: 2025-07-18 DOI: 10.1080/20565623.2025.2534329
Weilong Hua, Lijun Wang, Hongye Xu, Hongyu Ma, Yongxin Zhang, Hongjian Shen, Xiaoxi Zhang, Pengfei Xing, Pengfei Yang

Patients with systemic lupus erythematosus (SLE) typically have an increased risk of thrombosis, especially at a younger age. The prognosis of those acute ischemic stroke (AIS) patients due to acute intracranial artery occlusion seems to be favorable; however, with few published reports. We report two cases of AIS that were treated with intravenous thrombolysis (IVT) and mechanical thrombectomy (MT) with a prior diagnosis of SLE and were treated with regular oral corticosteroids before the onset. During the 1-year follow-up, these two patients were able to live normally without experiencing another ischemic stroke or changing medication. SLE-associated strokes necessitate urgent attention, with prompt diagnosis and immediate therapeutic measures, including thrombolytic therapy or MT, being crucial for achieving favorable patient outcomes.

系统性红斑狼疮(SLE)患者通常有血栓形成的风险增加,特别是在年轻时。急性颅内动脉闭塞所致急性缺血性脑卒中(AIS)患者预后良好;然而,发表的报告很少。我们报告了两例AIS患者,他们接受静脉溶栓(IVT)和机械取栓(MT)治疗,之前诊断为SLE,并在发病前接受常规口服皮质类固醇治疗。在1年的随访中,这两名患者能够正常生活,没有再发生缺血性中风或更换药物。sled相关中风需要紧急关注,及时诊断和立即治疗措施,包括溶栓治疗或MT,对于获得良好的患者预后至关重要。
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引用次数: 0
Liposomal honokiol enhance the anti-tumor effect of bevacizumab in glioblastoma by inhibiting autophagy. 脂质体厚朴醇通过抑制自噬增强贝伐单抗在胶质母细胞瘤中的抗肿瘤作用。
IF 2.1 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2025-12-01 Epub Date: 2025-08-13 DOI: 10.1080/20565623.2025.2546232
Pei Xun, Jiabao Zong, Shenglan Li, Wenbin Li

Aims: To investigate whether liposomal honokiol enhances the anti-tumor effect of bevacizumab (BEV) in glioblastoma (GBM) and explore its underlying mechanism.

Materials & methods: A U87 cell xenograft model in nude mice was used, with groups: model (M), M + liposomal honokiol (Lip-HNK), M + BEV, and M + Lip-HNK + BEV. Tumor volume, body weight, serum levels of VEGF, VEGFR, TNF-α, and Caspase-3, and expressions of autophagy-related (Beclin-1, LC3) and UPR-related (IRE1, GRP78) molecules in tumor tissues were detected.

Results: Compared with monotherapy, the combination of Lip-HNK and BEV significantly reduced tumor volume and tumor index, decreased serum levels of VEGF, VEGFR, and TNF-α, while increasing serum caspase-3. Further mechanistic studies showed that the combination of Lip-HNK and BEV significantly reduced the expression of Beclin-1, LC3, IRE1, and GRP78 in tumors.

Conclusions: Lip-HNK may promote the anti-GBM effect of BEV by inhibiting autophagy mediated by the UPR response.

目的:探讨脂质体厚木酚是否能增强贝伐珠单抗(BEV)对胶质母细胞瘤(GBM)的抗肿瘤作用,并探讨其机制。材料与方法:采用裸鼠U87细胞异种移植模型,分为模型(M)、M +脂质体厚朴酚(Lip-HNK)、M + BEV、M + Lip-HNK + BEV组。检测肿瘤体积、体重、血清VEGF、VEGFR、TNF-α、Caspase-3水平以及肿瘤组织中自噬相关分子(Beclin-1、LC3)和自噬相关分子(IRE1、GRP78)的表达。结果:与单药治疗相比,Lip-HNK联合BEV治疗可显著降低肿瘤体积和肿瘤指数,降低血清VEGF、VEGFR、TNF-α水平,升高血清caspase-3水平。进一步的机制研究表明Lip-HNK与BEV联合使用可显著降低肿瘤中Beclin-1、LC3、IRE1、GRP78的表达。结论:Lip-HNK可能通过抑制UPR反应介导的自噬来促进BEV的抗gbm作用。
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引用次数: 0
Reduced recurrence of prostate cancer with novel autologous cancer vaccine (FK- PC101) post-prostatectomy: long-term results from a single-center phase 1/2 study. 前列腺切除术后使用新型自体癌疫苗(FK- PC101)减少前列腺癌复发:一项单中心1/2期研究的长期结果
IF 2.1 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2025-12-01 Epub Date: 2025-08-29 DOI: 10.1080/20565623.2025.2550917
D M O Freitas, A C Stein, M Berger, F T Kreutz

Background: Prostate cancer is a major contributor to cancer-related mortality in men. High-risk patients, particularly those with biochemical recurrence (BCR) following radical prostatectomy (RP), face poor long-term outcomes. Adjuvant options such as radiotherapy, chemotherapy, and androgen deprivation therapy (ADT) have shown limited benefit in this setting.

Methods: This retrospective analysis evaluated the safety, feasibility, and efficacy of FK-PC101, an autologous immunomodulated tumor cell vaccine, in high-risk post-RP patients. Data were drawn from the FK002-2001 trial, a phase 1/2, non-randomized, open-label study conducted in Brazil. A total of 62 patients were included: 23 in the vaccine group and 39 controls. Primary endpoints were safety and feasibility; secondary endpoints included biochemical recurrence-free survival (BRFS) and overall survival (OS).

Results: The vaccine was well tolerated, with most adverse events being grade 1-2 local reactions. PSA recurrence at 4 years was significantly lower in the vaccine group (11.8%) when compared to controls (36.8%; P = 0.0453). OS did not differ significantly between groups. A higher rate of erectile dysfunction was observed in the vaccine group (P = 0.047).

Conclusion: FK-PC101 demonstrated safety and potential clinical benefit in reducing prostate specific antigen (PSA) recurrence after RP in high-risk prostate cancer patients. These findings support further evaluation in a randomized phase 2 trial.

背景:前列腺癌是男性癌症相关死亡的主要原因。高危患者,特别是根治性前列腺切除术(RP)后生化复发(BCR)的患者,长期预后较差。辅助选择如放疗、化疗和雄激素剥夺疗法(ADT)在这种情况下显示出有限的益处。方法:本回顾性分析评估了自体免疫调节肿瘤细胞疫苗FK-PC101在高危rp后患者中的安全性、可行性和有效性。数据来自FK002-2001试验,这是一项在巴西进行的1/2期、非随机、开放标签研究。共纳入62例患者:疫苗组23例,对照组39例。主要终点是安全性和可行性;次要终点包括生化无复发生存期(BRFS)和总生存期(OS)。结果:疫苗耐受性良好,大多数不良事件为1-2级局部反应。疫苗组4年PSA复发率(11.8%)明显低于对照组(36.8%,P = 0.0453)。各组间OS无显著差异。接种疫苗组勃起功能障碍发生率较高(P = 0.047)。结论:FK-PC101在高危前列腺癌RP术后降低前列腺特异性抗原(PSA)复发方面具有安全性和潜在的临床获益。这些发现支持在随机2期试验中进一步评估。
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引用次数: 0
Finger replantation in Jordan: evaluating the knowledge, attitudes, practices, and barriers among doctors and medical students. 约旦手指再植:评价医生和医学生的知识、态度、做法和障碍。
IF 2.1 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2025-12-01 Epub Date: 2025-09-08 DOI: 10.1080/20565623.2025.2557782
Saleh Abualhaj, Mosleh M Abualhaj, Lina Alshadfan, Anas As'ad, Mohamad Kharashgah, Tayseer A Al-Tawarah, Abed Alazeez Alkhatib, Mohammad Aljaidi

Background: Finger replantation is a complex microsurgical procedure that requires optimal conditions for success. Understanding the knowledge and awareness of healthcare professionals regarding finger preservation and replantation can help improve outcomes for patients with amputated fingers.

Methods: A cross-sectional survey was conducted among healthcare professionals, including clinical years medical students, surgical residents, and specialists. The survey assessed participants' knowledge of factors influencing the finger replantation success, the appropriate management of amputated fingers before surgery, the ideal time for replantation, and key considerations for finger preservation.

Results: Among 197 participants, 81.2% correctly identified finger replantation as a surgical procedure to reattach a severed finger. However, 9.6% incorrectly believed it was a technique to preserve the finger for later reattachment. The most frequently reported barriers to performing finger replantation included lack of training or expertise (78.2%), limited access to specialized surgical instruments (66.5%), and financial constraints (61.9%). Significant differences were found across professional groups regarding perceived barriers, particularly in terms of training, access to surgical instruments, and infrastructure.

Conclusion: While general knowledge of finger replantation is high, key misconceptions and barriers; like limited training, resources, and funding, persist. Improving education, infrastructure, and specialized programs is vital to expanding access and enhance outcomes.

背景:手指再植是一项复杂的显微外科手术,需要最佳的成功条件。了解医疗保健专业人员关于手指保存和再植的知识和意识有助于改善断指患者的预后。方法:对医疗保健专业人员进行横断面调查,包括临床医科学生、外科住院医师和专科医生。调查评估了参与者对影响手指再植成功的因素、手术前对断指的适当处理、再植的理想时间以及手指保存的关键考虑因素的了解。结果:在197名参与者中,81.2%的人正确地识别出手指再植术是再植断指的外科手术。然而,9.6%的人错误地认为这是一种保留手指以备以后再附着的技术。进行手指再植最常见的障碍包括缺乏培训或专业知识(78.2%),难以获得专门的手术器械(66.5%)和财政拮据(61.9%)。专业群体在感知障碍方面存在显著差异,特别是在培训、获得手术器械和基础设施方面。结论:对手指再植的认识较高,但存在一些误区和障碍;就像有限的培训、资源和资金一样,持续存在。改善教育、基础设施和专业项目对于扩大获取机会和提高成果至关重要。
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引用次数: 0
Diagnosing pulmonary MALT lymphoma: a case of unilateral cystic lesions. 肺MALT淋巴瘤诊断:单侧囊性病变1例。
IF 2.4 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2025-12-01 Epub Date: 2025-04-28 DOI: 10.1080/20565623.2025.2497214
Ping Li, Zhisheng Huang, Yan Qin, Wenjian Liao, Tianxin Xiang

We present an atypical case of a 62-year-old female diagnosed with pulmonary mucosa-associated lymphoid tissue (p-MALT) lymphoma, which uniquely manifested as a singular cystic lesion in the lung. Diagnostic evaluations, including comprehensive imaging, bronchoscopy, and CT-guided lung biopsy, revealed this uncommon radiological presentation. Detailed histopathological and immunohistochemical assessments further supported the diagnosis. To determine the extent of the disease, systemic evaluations, such as whole-body PET-CT, gastroscopy, colonoscopy, and bone marrow biopsy, were conducted, confirming its localized nature. Following the definitive diagnosis, the patient underwent a rituximab-centric therapeutic regimen, which yielded significant clinical improvement. This case highlights the importance of recognizing distinctive cystic lung features in p-MALT lymphoma and the indispensable role of holistic diagnostic approaches in guiding precise therapeutic and prognostic decisions.

我们提出一个不典型的病例62岁的女性诊断为肺粘膜相关淋巴组织(p-MALT)淋巴瘤,其独特的表现为一个单一的囊性病变在肺。诊断评估,包括综合影像学,支气管镜检查和ct引导下的肺活检,显示了这种罕见的放射表现。详细的组织病理学和免疫组织化学评估进一步支持诊断。为了确定疾病的程度,进行了全身PET-CT、胃镜、结肠镜和骨髓活检等系统评估,确认其局限性。确诊后,患者接受了以利妥昔单抗为中心的治疗方案,取得了显著的临床改善。该病例强调了识别p-MALT淋巴瘤独特的囊性肺特征的重要性,以及整体诊断方法在指导精确治疗和预后决策中不可或缺的作用。
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引用次数: 0
Causal effect of education on low back pain, intervertebral disc degeneration and sciatica: Mendelian randomization study. 教育对腰痛、椎间盘退变和坐骨神经痛的因果影响:孟德尔随机研究。
IF 2.1 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2025-12-01 Epub Date: 2025-11-26 DOI: 10.1080/20565623.2025.2590373
Zhihua Wu, Yiwei Gong, Haojun Long, Renhe Deng, Junhui He, Mingxuan Su, Jinyuan Wang, Kebo Gong

Background: Previous observational studies have examined the association between educational attainment (EA) and low back pain (LBP), intervertebral disc degeneration (IVDD), and sciatica. However, research is limited, and these findings are susceptible to reverse causality and confounding factors.

Methods: A two‑sample Mendelian randomization (MR) approach was applied to evaluate the associations of EA with LBP, IVDD, and sciatica, using publicly available summary statistics from large genome‑wide association studies (EBI, UK Biobank, and FinnGen) of European ancestry populations. A series of sensitivity analyses was conducted to assess the robustness of the findings.

Results: Higher genetically predicted educational attainment was associated with a lower risk of LBP, IVDD, and sciatica, although the effect magnitudes varied across cohorts. Protective associations were more evident in the FinnGen dataset, whereas results from the UK Biobank (UKB) and European Bioinformatics Institute (EBI) were directionally consistent but not statistically significant. The overall findings remained robust across multiple MR methods, with minimal evidence of pleiotropy.

Conclusions: Our findings suggest that higher educational attainment may have a protective effect against common spine-related disorders. Enhancing education‑related resources could support early prevention and reduce the population burden associated with these conditions.

背景:以前的观察性研究已经研究了受教育程度(EA)与腰痛(LBP)、椎间盘退变(IVDD)和坐骨神经痛之间的关系。然而,研究是有限的,这些发现容易受到反向因果关系和混杂因素的影响。方法:采用两样本的门德尔随机化(MR)方法来评估EA与LBP、IVDD和坐骨神经痛的关联,使用来自 欧洲 祖先 人群的大型全基因组关联研究(EBI、英国 Biobank和 FinnGen)的公开汇总统计数据。进行了一系列敏感性分析来评估研究结果的稳健性。结果:较高的遗传预测教育程度与较低的LBP、IVDD和坐骨神经痛风险相关,尽管影响程度在不同队列中有所不同。保护性关联在FinnGen数据集中更为明显,而来自英国生物银行(UKB)和欧洲生物信息学研究所(EBI)的结果方向一致,但没有统计学意义。多种MR方法的总体结果仍然稳定,多效性的证据很少。结论:我们的研究结果表明,较高的教育程度可能对常见的脊柱相关疾病有保护作用。加强与教育有关的资源可以支持早期预防并减少与这些疾病有关的人口负担。
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引用次数: 0
Lactate levels and heart failure: causal insights from Mendelian randomization and multi-cohort integrated analyses. 乳酸水平和心力衰竭:来自孟德尔随机化和多队列综合分析的因果见解。
IF 2.1 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2025-12-01 Epub Date: 2025-11-14 DOI: 10.1080/20565623.2025.2586994
Shijiu Jiang, Shuai Zhou, Runtian Dong, Yankai Xu, Haiying Hu, Kejian Liu

Objective: To explore the causal link between genetic predisposition for elevated lactate levels and heart failure (HF) via Mendelian randomization (MR), and investigate lactate-related genetic mechanisms and mediating pathways.

Methods: Lactate and HF summary data were from genome-wide association studies (GWAS). MR analyses used inverse variance weighting (IVW) as the main method; cardiac imaging trait MR focused on UK Biobank data. Mediation analysis examined CD20+ memory B cells' role in NUP50-HF pathway.

Results: MR showed that genetically predicted elevated lactate causally increased HF risk independent of hypoperfusion (reverse causality excluded) and reduced left ventricular ejection fraction (LVEF), implying a cardiac function-impairment pathway. NUP50, a key lactate-related gene, positively associated with HF. Its HF effect was partially mediated by CD20+ memory B cells; both independently linked to HF risk.

Conclusion: Elevated lactate may increase HF risk via impaired cardiac function. NUP50 and other lactate-related genes may regulate HF risk (NUP50 partially via CD20+ memory B cells), highlighting lactate and its genetic pathways as potential HF prevention/treatment targets.

目的:通过孟德尔随机化(Mendelian randomization, MR)研究乳酸水平升高与心力衰竭(heart failure, HF)的遗传易感性之间的因果关系,探讨乳酸相关的遗传机制和介导途径。方法:乳酸和心衰汇总数据来自全基因组关联研究(GWAS)。MR分析以方差逆加权(IVW)为主要方法;心脏成像特征MR聚焦于UK Biobank数据。中介分析检测CD20+记忆B细胞在NUP50-HF通路中的作用。结果:MR显示,基因预测乳酸升高会导致HF风险增加,而不依赖于低灌注(排除反向因果关系)和左室射血分数(LVEF)降低,这意味着心功能损害途径。NUP50是一个关键的乳酸相关基因,与HF呈正相关。其HF作用部分由CD20+记忆B细胞介导;两者都与HF风险独立相关。结论:乳酸水平升高可能通过心功能受损而增加心衰风险。NUP50和其他乳酸相关基因可能调节HF风险(NUP50部分通过CD20+记忆B细胞),强调乳酸及其遗传途径是潜在的HF预防/治疗靶点。
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引用次数: 0
Germline variants analysis of Chinese breast cancer patients reveals numerous alterations in homologous recombination genes. 中国乳腺癌患者的种系变异分析揭示了同源重组基因的许多改变。
IF 2.4 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2025-12-01 Epub Date: 2025-04-01 DOI: 10.1080/20565623.2025.2458432
Zhaoyun Jiang, Bing Xu, Bo Sun, Beibei Yang, Su Lu, Mengjian Li, Juan Zhang, Liqiang Qi, Qixi Wu

Purpose: We aimed to identify the pathogenic variants of homologous recombination (HR) genes and analyze the correlation between the pathogenic variants and clinical characteristics in Chinese breast cancer patients.

Methods: A cohort of 178 breast cancer patients participated in this study. We assessed genomic alterations using a 23-gene panel, which includes most of the HR-related genes and DNA mismatch repair (MMR) gene, through next-generation sequencing. The pathogenicity of variants was determined based on the American College of Medical Genetics and Genomics standards and guidelines. The correlation between these pathogenic variants and the clinical characteristics of the patients was investigated.

Results: 26 pathogenic variants, including one novel suspected pathogenic variant, were detected in 28 (15.7%) patients. These variants occurred in 7 HR-related genes: BRCA1, BRCA2, PALB2, RAD51D, RAD50, BRIP1, and ATM. The frequency of BRCA1 variants was higher in the younger group (8.9%) compared to the older group (2.6%), while the trend was reversed for BRCA2 (3.0% vs. 7.8%). All three patients with the pathogenic variant (p.Lys91fs) in RAD51D were diagnosed with triple-negative breast cancer.

Conclusions: HR-gene testing in breast cancer could help to find new suspected pathogenic variants and increase the clinical benefit of multi-gene testing for breast cancer.

目的:鉴定中国乳腺癌患者同源重组(homologous recombination, HR)基因的致病变异,并分析其致病变异与临床特征的相关性。方法:178例乳腺癌患者参与了这项研究。通过下一代测序,我们使用23个基因小组评估基因组改变,其中包括大多数hr相关基因和DNA错配修复(MMR)基因。变异的致病性是根据美国医学遗传学和基因组学学院的标准和指南确定的。研究了这些致病变异与患者临床特征的相关性。结果:28例(15.7%)患者共检出26种致病变异,其中1种为新型疑似致病变异。这些变异发生在7个hr相关基因中:BRCA1、BRCA2、PALB2、RAD51D、RAD50、BRIP1和ATM。BRCA1变异的频率在年轻组(8.9%)高于老年组(2.6%),而BRCA2的趋势则相反(3.0%对7.8%)。所有3例携带RAD51D致病变异(p.Lys91fs)的患者均被诊断为三阴性乳腺癌。结论:乳腺癌hr基因检测有助于发现新的疑似致病变异,增加乳腺癌多基因检测的临床获益。
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引用次数: 0
Unraveling the anoikis-cancer nexus: a bibliometric analysis of research trends and mechanisms. 揭示嗜酒与癌症的关系:研究趋势和机制的文献计量学分析。
IF 2.4 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2025-12-01 Epub Date: 2025-03-31 DOI: 10.1080/20565623.2025.2484159
Junjie Jiang, Wei Peng, Nianzhe Sun, Deze Zhao, Weifang Cui, Yuwei Lai, Chunfang Zhang, Chaojun Duan, Wei Zeng

Background: Cancer, influenced by genetics and the environment, involves anoikis, a cell death mechanism upon extracellular matrix detachment crucial for metastasis. Understanding this relationship is key for therapy. We analyze cancer and anoikis trends using bibliometrics.

Methods: A search was conducted from Web of Science Core, PubMed, Scopus and non-English databases such as the CNKI (inception- 21 December 2024). Data analysis employed Microsoft Excel, VOSviewer, CiteSpace, R software, and the online platform (https://bibliometric.com/).

Results: 2510 publications were retrieved, with a significant increase in the last decade. China led, the University of Texas system was productive, and the Oncogene Journal was popular. Breast, and colorectal cancers were frequently studied. Among them, representative tumor-related mechanisms were identified, commonalities such as (EMT, ECM, autophagy) and respective specific mechanisms were summarized.

Conclusion: This bibliometric analysis highlights rapid advances in anoikis research in cancer, emphasizing EMT and FAK pathways' translational potential, guiding targeted therapies, and improving cancer treatment outcomes.

背景:癌症受遗传和环境的影响,涉及细胞凋亡,细胞外基质脱落的细胞死亡机制,对转移至关重要。理解这种关系是治疗的关键。我们使用文献计量学分析癌症和疾病的趋势。方法:检索Web of Science Core、PubMed、Scopus和CNKI等非英文数据库(成立- 2024年12月21日)。数据分析采用Microsoft Excel、VOSviewer、CiteSpace、R软件和在线平台(https://bibliometric.com/).Results),共检索到2510篇出版物,近十年来有显著增长。中国带头,德克萨斯大学系统卓有成效,《致癌基因杂志》广受欢迎。乳腺癌和结直肠癌经常被研究。其中,确定了具有代表性的肿瘤相关机制,总结了EMT、ECM、自噬等共性及各自的具体机制。结论:这一文献计量学分析凸显了anoikis在癌症研究中的快速进展,强调了EMT和FAK通路的转化潜力,指导了靶向治疗,改善了癌症治疗结果。
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引用次数: 0
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