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miR-216a 通过下调 KIAA1199/CEMIP 抑制结直肠癌的侵袭和转移。

Down-regulation of KIAA1199/CEMIP by miR-216a suppresses tumor invasion and metastasis in colorectal cancer.

机构信息

Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China

Department of Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China

出版信息

Int J Cancer. 2017 May 15;140(10):2298-2309. doi: 10.1002/ijc.30656. Epub 2017 Mar 2.

DOI:10.1002/ijc.30656
PMID:28213952
Abstract

Colorectal cancer is one of the major causes of death from cancer. Metastasis is the leading cause of treatment failure, in which cancer stem cells and circulating tumor cells play crucial roles. Identifying the involved metastatic biomarkers and clarifying the regulation mechanisms are of great importance for targeting tumor metastasis. In the current research, we discovered that KIAA1199, a cell-migration inducing protein, showed higher expression in CD44+ cancer cells from metastatic compared with the paired primary tissues, and was upregulated in colorectal cancer and positively correlated with numbers and mesenchymal phenotype of circulating tumor cells, and predicted shorter progress-free survival. Moreover, we indicated that down-regulation of KIAA1199 suppressed migration and invasion of colorectal cancer cells in vitro, and inhibited metastasis in vivo. Furthermore, we demonstrated that KIAA1199 was one of the direct and functional targets of miR-216a, and miR-216a overexpression led to decreased migration and invasion of colorectal cancer cells in vitro, and inhibited metastasis in vivo. Collectively, KIAA1199 plays a critical role in maintaining an aggressive phenotype of tumor cells, and suppression of KIAA1199-related motilities of tumor cells contributes to reduced tumor metastasis in colorectal cancer.

摘要

结直肠癌是癌症死亡的主要原因之一。转移是治疗失败的主要原因,其中癌症干细胞和循环肿瘤细胞起着至关重要的作用。鉴定涉及的转移生物标志物并阐明调节机制对于靶向肿瘤转移非常重要。在目前的研究中,我们发现,KIAA1199 是一种诱导细胞迁移的蛋白,在转移性 CD44+ 癌细胞中的表达高于配对的原发性组织,在结直肠癌中上调,并与循环肿瘤细胞的数量和间充质表型呈正相关,预测无进展生存期更短。此外,我们表明,下调 KIAA1199 抑制了体外结直肠癌细胞的迁移和侵袭,并抑制了体内转移。此外,我们证明 KIAA1199 是 miR-216a 的直接和功能靶标之一,过表达 miR-216a 导致体外结直肠癌细胞迁移和侵袭减少,并抑制体内转移。总之,KIAA1199 在维持肿瘤细胞的侵袭表型中起着关键作用,抑制肿瘤细胞的 KIAA1199 相关运动有助于减少结直肠癌的肿瘤转移。

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