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

被引:26
|
作者
Naemura, Madoka [1 ]
Tsunoda, Toshiyuki [3 ]
Inoue, Yasutoshi [1 ]
Okamoto, Haruna [1 ]
Shirasawa, Senji [3 ]
Kotake, Yojiro [1 ,2 ]
机构
[1] Kinki Univ, Grad Sch Humanity Oriented Sci & Engn, 11-6 Kayanomori, Iizuka, Fukuoka 8208555, Japan
[2] Kinki Univ, Fac Humanity Oriented Sci & Engn, Dept Biol & Environm Chem, 11-6 Kayanomori, Iizuka, Fukuoka 8208555, Japan
[3] Fukuoka Univ, Dept Cell Biol, Fac Med, Jonan Ku, 7-45-1 Nanakuma, Fukuoka 8140180, Japan
关键词
Long noncoding RNA; ANRIL; p15; p16; Colorectal cancer; Cell cycle; LONG NONCODING RNAS; TUMOR-SUPPRESSOR GENE; LUNG-CANCER; INK4A LOCUS; CRYPT MODEL; INHIBITION; P16(INK4A); P19(ARF); PRODUCT; MDM2;
D O I
10.1007/s11010-015-2618-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:141 / 146
页数:6
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