Motile sperm domain containing 1 is upregulated by the Wnt/β-catenin signaling pathway in colorectal cancer

被引:5
作者
Horie, Chiaki [1 ]
Zhu, Chi [1 ]
Yamaguchi, Kiyoshi [1 ,4 ]
Nakagawa, Saya [1 ]
Isobe, Yumiko [1 ]
Takane, Kiyoko [1 ]
Ikenoue, Tsuneo [1 ]
Ohta, Yasunori [2 ]
Tanaka, Yukihisa [2 ]
Aikou, Susumu [3 ]
Tsurita, Giichiro [3 ]
Ahiko, Yuka [3 ]
Shida, Dai [3 ]
Furukawa, Yoichi [1 ]
机构
[1] Univ Tokyo, Inst Med Sci, Adv Clin Res Ctr, Div Clin Genome Res, Tokyo 1088639, Japan
[2] Univ Tokyo, Res Hosp, Inst Med Sci, Dept Pathol, Tokyo 1088639, Japan
[3] Univ Tokyo, Res Hosp, Inst Med Sci, Dept Surg, Tokyo 1088639, Japan
[4] Univ Tokyo, Inst Med Sci, Adv Clin Res Ctr, Div Clin Genome Res, 4-6-1 Shirokanedai,Minato Ku, Tokyo 1088639, Japan
基金
日本学术振兴会;
关键词
motile sperm domain containing 1; Wnt; beta-catenin; transcription factor 7 like 2; colorectal cancer; BETA-CATENIN; WNT SECRETION; C-MYC; IDENTIFICATION; TRANSCRIPTION; EXPRESSION; TARGET; GENE; PROLIFERATION; COMPLEX;
D O I
10.3892/ol.2022.13402
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aberrant activation of the Wnt/beta-catenin signaling pathway plays a crucial role in the development and progression of colorectal cancer. Previously, we identified a set of candidate genes that were regulated by this signaling pathway, and the present study focused on motile sperm domain containing 1 (MOSPD1). Immunohistochemical staining revealed that the expression of MOSPD1 was elevated in tumor cells from colorectal cancer tissues compared with in non-tumor cells. Using ChIP-seq data and the JASPAR database, the regulatory region(s) in the MOSPD1 gene as a target of the Wnt/beta-catenin signaling pathway were searched, and a region containing three putative TCF-binding motifs in the 3'-flanking region was identified. Additional analyses using reporter assay and ChIP-quantitative PCR suggested that this region harbors enhancer activity through an interaction with transcription factor 7 like 2 (TCF7L2) and beta-catenin. In addition, chromatin conformation capture assay revealed that the 3 & PRIME;-flanking region interacts with the MOSPD1 promoter. These data suggested that MOSPD1 was regulated by the beta-catenin/TCF7L2 complex through the enhancer element located in the 3 & PRIME;-flanking region. These findings may be helpful for future studies regarding the precise regulatory mechanisms of MOSPD1.
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页数:8
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