Hypermethylation of NDN promotes cell proliferation by activating the Wnt signaling pathway in colorectal cancer

被引:15
作者
Hu, Yu-Han [1 ,2 ]
Chen, Qing [3 ]
Lu, Yan-Xia [1 ]
Zhang, Jian-Ming [1 ,3 ]
Lin, Chun [1 ]
Zhang, Fan [1 ]
Zhang, Wen-Juan [1 ]
Li, Xiao-Min [1 ]
Zhang, Wei [1 ]
Li, Xue-Nong [1 ]
机构
[1] Southern Med Univ, Sch Basic Med Sci, Dept Pathol, Guangzhou, Guangdong, Peoples R China
[2] Xinxiang Med Univ, Dept Pathol, Xinxiang, Peoples R China
[3] Southern Med Univ, Nanfang Hosp, Dept Surg, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
NDN; LRP6; Wnt signaling pathway; colorectal cancer; proliferation; TUMOR-SUPPRESSOR GENE; WNT/BETA-CATENIN PATHWAY; COLON-CANCER; NECDIN; METASTASIS; GROWTH; INTERACTS; PROTEINS; TUMORIGENESIS; TRANSCRIPTION;
D O I
10.18632/oncotarget.17580
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The progression of CRC is a multistep process involving several genetic changes or epigenetic modifications. NDN is a member of the MAGE family, encoding a protein that generally suppresses cell proliferation and acting as a transcriptional repressor. Immunohistochemical staining revealed that the expression of NDN was significantly down-regulated in CRC tissues compared with normal tissues and the down-regulation of NDN in CRC could reflect the hypermethylation of the NDN promoter. Treatment of the CRC cell line SW480 with the demethylating agent 5-Aza-CdR restored the NDN expression level. The down-regulation of NDN was closely related to poor differentiation, advanced TNM stage and poor prognosis of CRC. The inhibition of NDN promoted CRC cell proliferation by enriching cells in the S phase. Furthermore, we observed that NDN binds to the GN box in the promoter of LRP6 to attenuate LRP6 transcription and inhibit the Wnt signaling pathway in CRC. In conclusion, our study revealed that the hypermethylation of NDN promotes cell proliferation by activating the Wnt signaling pathway through directly increasing the transcription of LRP6 in CRC. These findings might provide a new theoretical basis for the pathogenesis of CRC and facilitate the development of new therapeutic strategies against CRC.
引用
收藏
页码:46191 / 46203
页数:13
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