TMEM35B as a novel biomarker for diagnosing gliomas.

IF 1.9 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Biomarkers in medicine Pub Date : 2024-12-01 Epub Date: 2024-11-26 DOI:10.1080/17520363.2024.2431480
Gongbo Liang, Xuwen Lai, Guangning Yan, Wenyuan He, Longjun Su, Jinxia Luo, Zhuocai Wang
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Abstract

Aims: There is little information about transmembrane protein 35B (TMEM35B) expression in glioma, and its functions in glioma remains no clue.

Patients & methods: Immunohistochemistry was used to measure TMEM35B expression levels and CCK8 and Transwell assays were analyzed the proliferative and migratory and invasive.

Results: TMEM35B protein was significantly higher in gliomas and correlated with a higher tumor TNM stages. Receiver operating characteristic curve analysis revealed that TMEM35B had high diagnostic value in distinguishing among glioma, normal tissues, tumor stages III+IV, and I+II. Additionally, TMEM35B knockdown inhibited the proliferative, migratory, and invasive capacities of glioma cells.

Conclusions: TMEM35B expression is upregulated in gliomas, and its knockdown hinders tumor progression, highlighting the protein as a potential biomarker for glioma diagnosis.

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TMEM35B 作为诊断胶质瘤的新型生物标记物。
目的:有关跨膜蛋白35B(TMEM35B)在胶质瘤中表达的信息很少,其在胶质瘤中的功能仍无线索:免疫组化法测定TMEM35B的表达水平,CCK8和Transwell试验分析其增殖性、迁移性和侵袭性:结果:TMEM35B蛋白在胶质瘤中的表达量明显较高,且与肿瘤的TNM分期相关。接收者操作特征曲线分析显示,TMEM35B 在区分胶质瘤、正常组织、肿瘤 III+IV 期和 I+II 期方面具有很高的诊断价值。此外,TMEM35B敲除抑制了胶质瘤细胞的增殖、迁移和侵袭能力:结论:TMEM35B在胶质瘤中表达上调,其敲除会阻碍肿瘤的进展,因此该蛋白有望成为胶质瘤诊断的生物标记物。
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来源期刊
Biomarkers in medicine
Biomarkers in medicine 医学-医学:研究与实验
CiteScore
3.80
自引率
4.50%
发文量
86
审稿时长
6-12 weeks
期刊介绍: Biomarkers are physical, functional or biochemical indicators of physiological or disease processes. These key indicators can provide vital information in determining disease prognosis, in predicting of response to therapies, adverse events and drug interactions, and in establishing baseline risk. The explosion of interest in biomarker research is driving the development of new predictive, diagnostic and prognostic products in modern medical practice, and biomarkers are also playing an increasingly important role in the discovery and development of new drugs. For the full utility of biomarkers to be realized, we require greater understanding of disease mechanisms, and the interplay between disease mechanisms, therapeutic interventions and the proposed biomarkers. However, in attempting to evaluate the pros and cons of biomarkers systematically, we are moving into new, challenging territory. Biomarkers in Medicine (ISSN 1752-0363) is a peer-reviewed, rapid publication journal delivering commentary and analysis on the advances in our understanding of biomarkers and their potential and actual applications in medicine. The journal facilitates translation of our research knowledge into the clinic to increase the effectiveness of medical practice. As the scientific rationale and regulatory acceptance for biomarkers in medicine and in drug development become more fully established, Biomarkers in Medicine provides the platform for all players in this increasingly vital area to communicate and debate all issues relating to the potential utility and applications. Each issue includes a diversity of content to provide rounded coverage for the research professional. Articles include Guest Editorials, Interviews, Reviews, Research Articles, Perspectives, Priority Paper Evaluations, Special Reports, Case Reports, Conference Reports and Company Profiles. Review coverage is divided into themed sections according to area of therapeutic utility with some issues including themed sections on an area of topical interest. Biomarkers in Medicine provides a platform for commentary and debate for all professionals with an interest in the identification of biomarkers, elucidation of their role and formalization and approval of their application in modern medicine. The audience for Biomarkers in Medicine includes academic and industrial researchers, clinicians, pathologists, clinical chemists and regulatory professionals.
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