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ANRIL在二维和三维培养中均调控人结肠癌细胞的增殖。

ANRIL regulates the proliferation of human colorectal cancer cells in both two- and three-dimensional culture.

作者信息

Naemura Madoka, Tsunoda Toshiyuki, Inoue Yasutoshi, Okamoto Haruna, Shirasawa Senji, Kotake Yojiro

机构信息

Graduate School of Humanity-Oriented Science and Engineering, Kinki University, 11-6 Kayanomori, Iizuka, Fukuoka, 820-8555, Japan.

Department of Cell Biology, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180, Japan.

出版信息

Mol Cell Biochem. 2016 Jan;412(1-2):141-6. doi: 10.1007/s11010-015-2618-5. Epub 2015 Dec 26.

Abstract

ANRIL is a long noncoding RNA transcribed from the INK4 locus that encodes three tumor suppressor genes, p15, p16, and ARF. Previous studies demonstrated that ANRIL represses p15 and p16, which positively regulate the pRB pathway, leading to repression of cellular senescence of human normal fibroblasts. However, the role of ANRIL in cancer cell proliferation is less well understood. Here we report that ANRIL is involved in the proliferation of colorectal cancer HCT116 cells in two- and three-dimensional culture. Silencing ANRIL by both transfection with small interfering RNA and retrovirally produced small hairpin RNA reduced HCT116 cell proliferation in both two- and three-dimensional culture. HCT116 cells depleted for ANRIL were arrested in the S phase of cell cycle. Notably, silencing ANRIL did not result in the activation of expression of the INK4 locus. These results suggest that ANRIL positively regulates the proliferation of HCT116 cells in two- and three-dimensional culture in a p15/p16-pRB pathway-independent manner.

摘要

ANRIL是一种从INK4基因座转录而来的长链非编码RNA,该基因座编码三种肿瘤抑制基因,即p15、p16和ARF。先前的研究表明,ANRIL可抑制p15和p16,而p15和p16可正向调节pRB通路,从而导致人正常成纤维细胞的细胞衰老受到抑制。然而,ANRIL在癌细胞增殖中的作用尚不太清楚。在此我们报告,ANRIL在二维和三维培养中参与结肠直肠癌HCT116细胞的增殖。通过转染小干扰RNA和逆转录病毒产生的小发夹RNA使ANRIL沉默,均可降低二维和三维培养中HCT116细胞的增殖。缺失ANRIL的HCT116细胞停滞在细胞周期的S期。值得注意的是,沉默ANRIL并未导致INK4基因座表达的激活。这些结果表明,ANRIL以一种不依赖p15/p16-pRB通路的方式正向调节二维和三维培养中HCT116细胞的增殖。

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