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孤儿核受体 EAR2 在结直肠癌中过表达,它调节结肠癌细胞的存活能力。

The orphan nuclear receptor EAR2 is overexpressed in colorectal cancer and it regulates survivability of colon cancer cells.

机构信息

The Key Laboratory of Nutrition and Metabolism, Institute for Nutritional Sciences, Shanghai Institute for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.

出版信息

Cancer Lett. 2011 Oct 28;309(2):137-44. doi: 10.1016/j.canlet.2011.05.025. Epub 2011 Jun 22.

Abstract

EAR2 is a member of the chick ovalbumin upstream promoter-transcription factors (COUP-TFs). COUP-TFs belong to orphan nuclear receptors and regulate many biological processes. Little is known regarding EAR2 in cancer, though much progress has been made in understanding the function of other COUP-TF members. The aim of this study is to investigate the expression and possible function of EAR2 in colorectal cancer. We determined expression of EAR2 in human primary colorectal malignant tumors and their paired adjacent normal colorectal tissues. We found that expression of EAR2 was upregulated in colorectal tumors. Knockdown of EAR2 induced apoptosis of colon cancer cells, suggesting that EAR2 may function to regulate survivability of colon cancer cells. In vivo tumor study demonstrated that knockdown of EAR2 inhibited the xenograft growth of colon cancer cells. We found that knockdown of EAR2 inhibited the expression of X-linked inhibitor of apoptosis protein (XIAP), suggesting that EAR2 regulates cell survivability, at least partly, through XIAP. In this manuscript, we demonstrated that expression of EAR2 was elevated in colorectal cancer and knockdown of EAR2 reduced survivability and tumor growth of colon cancer cells. Our results suggest that EAR2 plays an important role in development of colorectal cancer. The findings also suggest that EAR2 may serve as a potential therapeutic target of colorectal cancer.

摘要

EAR2 是鸡卵清蛋白上游启动子转录因子 (COUP-TFs) 的成员。COUP-TFs 属于孤儿核受体,调节许多生物过程。尽管人们对其他 COUP-TF 成员的功能有了很多了解,但对 EAR2 在癌症中的作用知之甚少。本研究旨在探讨 EAR2 在结直肠癌中的表达及其可能的功能。我们测定了人原发性结直肠恶性肿瘤及其配对的相邻正常结直肠组织中 EAR2 的表达。结果发现,EAR2 在结直肠肿瘤中表达上调。EAR2 的敲低诱导结肠癌细胞凋亡,提示 EAR2 可能调节结肠癌细胞的存活能力。体内肿瘤研究表明,EAR2 的敲低抑制了结肠癌细胞的异种移植生长。我们发现,EAR2 的敲低抑制了凋亡抑制蛋白 X 连锁因子 (XIAP) 的表达,提示 EAR2 通过 XIAP 调节细胞存活能力,至少部分如此。在本研究中,我们证明了 EAR2 在结直肠癌中的表达升高,EAR2 的敲低降低了结肠癌细胞的存活能力和肿瘤生长。我们的结果表明,EAR2 在结直肠癌的发生发展中起重要作用。这些发现还表明,EAR2 可能成为结直肠癌的潜在治疗靶点。

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