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跨膜蛋白211促进结肠癌的肿瘤进展和转移。

TMEM211 Promotes Tumor Progression and Metastasis in Colon Cancer.

作者信息

Chang Yung-Fu, Wang Hsing-Hsang, Shu Chih-Wen, Tsai Wei-Lun, Lee Cheng-Hsin, Chen Chun-Lin, Liu Pei-Feng

机构信息

Department of Biomedical Science and Environmental Biology, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.

Translational Research Center of Neuromuscular Diseases, Kaohsiung Medical University Hospital, Kaohsiung 80708, Taiwan.

出版信息

Curr Issues Mol Biol. 2023 May 24;45(6):4529-4543. doi: 10.3390/cimb45060287.

Abstract

Colon cancer is the third most important cancer type, leading to a remarkable number of deaths, indicating the necessity of new biomarkers and therapeutic targets for colon cancer patients. Several transmembrane proteins (TMEMs) are associated with tumor progression and cancer malignancy. However, the clinical significance and biological roles of TMEM211 in cancer, especially in colon cancer, are still unknown. In this study, we found that TMEM211 was highly expressed in tumor tissues and the increased TMEM211 was associated with poor prognosis in colon cancer patients from The Cancer Genome Atlas (TCGA) database. We also showed that abilities regarding migration and invasion were reduced in TMEM211-silenced colon cancer cells (HCT116 and DLD-1). Moreover, TMEM211-silenced colon cancer cells showed decreased levels of Twist1, N-cadherin, Snail and Slug but increased levels of E-cadherin. Levels of phosphorylated ERK, AKT and RelA (NF-κB p65) were also decreased in TMEM211-silenced colon cancer cells. Our findings indicate that TMEM211 regulates epithelial-mesenchymal transition for metastasis through coactivating the ERK, AKT and NF-κB signaling pathways, which might provide a potential prognostic biomarker or therapeutic target for colon cancer patients in the future.

摘要

结肠癌是第三大重要癌症类型,导致大量死亡,这表明有必要为结肠癌患者寻找新的生物标志物和治疗靶点。几种跨膜蛋白(TMEMs)与肿瘤进展和癌症恶性程度相关。然而,TMEM211在癌症尤其是结肠癌中的临床意义和生物学作用仍不清楚。在本研究中,我们发现TMEM211在肿瘤组织中高表达,且在来自癌症基因组图谱(TCGA)数据库的结肠癌患者中,TMEM211表达增加与预后不良相关。我们还表明,在TMEM211沉默的结肠癌细胞(HCT116和DLD-1)中,迁移和侵袭能力降低。此外,TMEM211沉默的结肠癌细胞中Twist1、N-钙黏蛋白、Snail和Slug水平降低,但E-钙黏蛋白水平升高。TMEM211沉默的结肠癌细胞中磷酸化的ERK、AKT和RelA(NF-κB p65)水平也降低。我们的研究结果表明,TMEM211通过共激活ERK、AKT和NF-κB信号通路调节上皮-间质转化以促进转移,这可能为未来结肠癌患者提供潜在的预后生物标志物或治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a546/10297151/2b87d40b1969/cimb-45-00287-g001.jpg

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