Zhang Dan, Bi Jiaxin, Liang Qiaoyan, Wang Shuyang, Zhang Lingjie, Han Fangyi, Li Shengnan, Qiu Bowen, Fan Xingdi, Chen Wei, Jiao Hongli, Ye Yaping, Ding Yanqing
Department of Pathology, School of Basic Medical Sciences and Nanfang Hospital, Southern Medical University, Guangzhou, China.
Guangdong Provincial Key Laboratory of Molecular Tumor Pathology, Guangzhou, China.
Front Oncol. 2020 Jul 23;10:1066. doi: 10.3389/fonc.2020.01066. eCollection 2020.
Vascular cell adhesion molecular 1 (VCAM1), an important member of the immunoglobulin superfamily, is related to the development of malignant tumors, such as breast cancer, melanoma, and renal clear cell carcinoma. However, the molecular role and mechanism of VCAM1 in the regulation of the progression of colorectal cancer (CRC) has rarely been studied. The results of IHC and RT-PCR analyses proved that VCAM1 was upregulated in human CRC tissues compared with matched adjacent normal intestinal epithelial tissues. Moreover, analysis of data from the TCGA and Gene Expression Omnibus (GEO) databases revealed that a higher level of VCAM1 was strongly correlated with poor differentiation, metastasis, and short survival in CRC patients. Furthermore, VCAM1 significantly influenced the invasion and metastasis of CRC cells and and activated the EMT program, by which cancer cells adhere to the endothelium and cross the vessel wall by forming pseudopodia and invadopodia. The current findings demonstrate that VCAM1 promotes tumor progression in CRC.
血管细胞黏附分子1(VCAM1)是免疫球蛋白超家族的重要成员,与乳腺癌、黑色素瘤和肾透明细胞癌等恶性肿瘤的发生发展有关。然而,VCAM1在结直肠癌(CRC)进展调控中的分子作用和机制鲜有研究。免疫组化(IHC)和逆转录聚合酶链反应(RT-PCR)分析结果证明,与配对的相邻正常肠上皮组织相比,VCAM1在人CRC组织中表达上调。此外,对来自癌症基因组图谱(TCGA)和基因表达综合数据库(GEO)的数据进行分析发现,较高水平的VCAM1与CRC患者的低分化、转移及生存期短密切相关。此外,VCAM1显著影响CRC细胞的侵袭和转移,并激活上皮-间质转化(EMT)程序,癌细胞通过该程序黏附于内皮细胞,并通过形成伪足和侵袭伪足穿过血管壁。目前的研究结果表明,VCAM1促进CRC的肿瘤进展。