| Literature DB >> 28235487 |
Hidefumi Taniguchi1, Saya Ito2, Takashi Ueda3, Yukako Morioka1, Naruhiro Kayukawa1, Akihisa Ueno1, Hideo Nakagawa1, Atsuko Fujihara1, So Ushijima1, Motohiro Kanazawa1, Fumiya Hongo1, Osamu Ukimura1.
Abstract
Renal cell carcinoma (RCC) is the most common type of kidney cancer. However, the mechanisms underlying the progression of the disease are not well understood. The data in this report suggest that canopy FGF signaling regulator 2 (CNPY2) is a promoter of RCC progression. We found that CNPY2 significantly promoted growth of RCC cells and upregulated TP53 gene expression. Although TP53 is widely known as a tumor suppressor, in RCC TP53 promoted tumor cell growth. A typical p53 target gene, CDKN1A, was upregulated by both p53 and CNPY2 in RCC cells, suggesting that CNPY2 increased the expression level of TP53. Consistent with these results, CNPY2 and TP53 expression levels were positively correlated in RCC patients. These findings suggested that CNPY2 promoted cancer cell growth in RCC through regulating TP53 gene expression.Entities:
Keywords: CNPY2; Renal cell carcinoma; p53
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Year: 2017 PMID: 28235487 DOI: 10.1016/j.bbrc.2017.02.095
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575