TSPAN1过表达是雌激素受体阳性乳腺癌预后不良的指标。

IF 1.5 4区 医学 Q4 ONCOLOGY Translational cancer research Pub Date : 2024-08-31 Epub Date: 2024-08-21 DOI:10.21037/tcr-24-409
Xiangjuan Liu, Jiahong Zhang, Jun Zhao, Yan Cheng, Dandan Jiang
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引用次数: 0

摘要

背景:Tetraspanin 1(TSPAN1)是一种新发现的四聚体蛋白家族蛋白,由位于 1p34 染色体区域的 TSPAN1 基因编码。已有研究表明,TSPAN1 与多种恶性肿瘤有关。本研究旨在探讨 TSPAN1 在乳腺癌中的预后意义。雌激素受体阳性(ER+)乳腺癌是最大的乳腺癌亚组,ER靶向疗法显著延长了晚期乳腺癌患者的生存期并改善了症状。研究发现,TSPAN1的过表达与ER+乳腺癌的不良预后有关:方法:我们采用免疫印迹法和定量反转录聚合酶链反应(RT-qPCR)分析了TSPAN1在乳腺癌组织和细胞系中的表达情况:结果:与正常乳腺组织相比,TSPAN1在乳腺癌细胞中的表达量更高。结果发现:与正常乳腺组织相比,TSPAN1 在乳腺癌细胞中的表达量更高。抑制 TSPAN1 能显著减少 BT474 细胞在体外和体内的增殖和侵袭。下调乳腺癌细胞中的TSPAN1可显著降低p-丝裂原活化蛋白激酶1(MEK1)(S298)和p-细胞外信号调节激酶(ERK)1/2的水平:结论:TSPAN1 可调节下游细胞外基质(ECM)受体信号级联,促进乳腺癌的细胞增殖和侵袭。抑制 TSPAN1 可能是一种潜在的乳腺癌治疗新策略。
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TSPAN1 overexpression as an indicator of poor prognosis in estrogen receptor-positive breast cancer.

Background: Tetraspanin 1 (TSPAN1) is a newly discovered protein of the tetrameric protein family encoded by the TSPAN1 gene localized in the 1p34 chromosome region. TSPAN1 has been shown to be associated with various malignancies. In this study, we aimed to investigate the prognostic significance of TSPAN1 in breast cancer. Estrogen receptor-positive (ER+) breast cancer is the largest breast cancer subgroup, and ER-targeted therapies have significantly prolonged survival and improved symptoms in advanced breast cancer. TSPAN1 overexpression was found to be associated with a poor prognosis in ER+ breast cancer.

Methods: We analyzed the expression of TSPAN1 in breast cancer tissues and cell lines using western blotting and quantitative reverse transcription polymerase chain reaction (RT-qPCR).

Results: TSPAN1 expression was higher in breast cancer cells as compared with normal breast tissue. There was a significant association between a high TSPAN1 level and a low survival rate. Inhibition of TSPAN1 significantly reduced the proliferation and invasion of BT474 cells both in vitro and in vivo. The downregulation of TSPAN1 in breast cancer cells significantly reduced the levels of p-mitogen-activated protein kinase 1 (MEK1) (S298) and p-extracellular signal-regulating kinase (ERK) 1/2.

Conclusions: TSPAN1 modulates downstream extracellular matrix (ECM) receptor signaling cascades and promotes cellular proliferation and invasion in breast cancer. TSPAN1 inhibition may be a potential new treatment strategy for breast cancer.

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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
252
期刊介绍: Translational Cancer Research (Transl Cancer Res TCR; Print ISSN: 2218-676X; Online ISSN 2219-6803; http://tcr.amegroups.com/) is an Open Access, peer-reviewed journal, indexed in Science Citation Index Expanded (SCIE). TCR publishes laboratory studies of novel therapeutic interventions as well as clinical trials which evaluate new treatment paradigms for cancer; results of novel research investigations which bridge the laboratory and clinical settings including risk assessment, cellular and molecular characterization, prevention, detection, diagnosis and treatment of human cancers with the overall goal of improving the clinical care of cancer patients. The focus of TCR is original, peer-reviewed, science-based research that successfully advances clinical medicine toward the goal of improving patients'' quality of life. The editors and an international advisory group of scientists and clinician-scientists as well as other experts will hold TCR articles to the high-quality standards. We accept Original Articles as well as Review Articles, Editorials and Brief Articles.
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