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C/EBPα 诱导的 miR-100 通过靶向胃癌中的 ZBTB7A 抑制肿瘤转移和生长。

C/EBPα-induced miR-100 expression suppresses tumor metastasis and growth by targeting ZBTB7A in gastric cancer.

机构信息

Department of Pathology, Qilu Hospital, Shandong University, Jinan 250012, China.

Department of Pathology, Qilu Hospital, Shandong University, Jinan 250012, China.

出版信息

Cancer Lett. 2015 Dec 28;369(2):376-85. doi: 10.1016/j.canlet.2015.08.029. Epub 2015 Sep 25.

Abstract

MicroRNAs have been reported to play key roles in various human cancers, including gastric cancer. However, understanding of the expression of miR-100 and its regulatory mechanisms in human gastric cancer remains elusive. In this study, we reveal that miR-100 is downregulated in gastric cancer samples and gastric cancer cell lines. Furthermore, lower miR-100 expression was found in primary gastric cancer samples with lymphatic metastasis compared to those without lymphatic metastasis. Overexpression of miR-100 suppressed tumor growth in vivo and inhibited gastric cancer invasion and metastasis in vitro and in vivo. Furthermore, we demonstrated that miR-100 reduced gastric cancer aggressiveness by directly targeting ZBTB7A. Knockdown of ZBTB7A by siRNA disrupted gastric cancer progression by impairing tumor invasion and metastasis. High expression of ZBTB7A was significantly correlated with poorer prognosis in gastric cancer patients. Our results also showed that the transcription factor CCAAT/enhancer-binding protein alpha (C/EBPα) could induce the expression of miR-100 by binding to the putative promoter region of miR-100. This study demonstrated that miR-100 could be induced by C/EBPα and may act as a tumor suppressor gene by inhibiting ZBTB7A.

摘要

MicroRNAs 已被报道在多种人类癌症中发挥关键作用,包括胃癌。然而,miR-100 在人类胃癌中的表达及其调控机制仍不清楚。在这项研究中,我们揭示了 miR-100 在胃癌样本和胃癌细胞系中下调。此外,与无淋巴转移的原发性胃癌样本相比,具有淋巴转移的原发性胃癌样本中 miR-100 的表达水平较低。miR-100 的过表达抑制了体内肿瘤的生长,并抑制了体外和体内胃癌的侵袭和转移。此外,我们证明 miR-100 通过直接靶向 ZBTB7A 来降低胃癌的侵袭性。通过 siRNA 敲低 ZBTB7A 会破坏肿瘤侵袭和转移,从而扰乱胃癌的进展。ZBTB7A 的高表达与胃癌患者的预后不良显著相关。我们的研究结果还表明,转录因子 CCAAT/增强子结合蛋白α(C/EBPα)可以通过结合 miR-100 的启动子区域来诱导 miR-100 的表达。本研究表明,miR-100 可以被 C/EBPα 诱导,并且可能通过抑制 ZBTB7A 而作为一种肿瘤抑制基因发挥作用。

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