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p53过表达抑制前列腺癌细胞系中雄激素介导的NKX3.1诱导。

p53 overexpression represses androgen-mediated induction of NKX3.1 in a prostate cancer cell line.

作者信息

Jiang Anli, Yu Chunxiao, Zhang Pengju, Chen Weiwen, Liu Wenwen, Hu Xiaoyan, Zhang Jianye

机构信息

Department of Biochemistry, Medical School of Shandong University, Jinan 250012, China.

出版信息

Exp Mol Med. 2006 Dec 31;38(6):625-33. doi: 10.1038/emm.2006.74.

Abstract

Prostate cancer is a disease involving complicated multiple-gene alterations. Both NKX3.1 and p53 are related to prostate cancer and play crucial roles in prostate cancer progression. However, little is known about the relationships and interactions between p53 and NKX3.1 in prostate cancer. We found that NKX3.1 expression is down-regulated by over-expression of wild type (wt) p53 in prostate cancer LNCaP cells. NKX3.1 is down-regulated at both the mRNA and protein levels by p53 over- expression due to either transient transfection of exogenous p53 or induction of endogenous p53. p53 over-expression represses androgen-induced transactivation of NKX3.1 by inhibiting the promoter of the androgen acceptor (AR) gene and by blocking AR-DNA binding activity. In addition, transfection with the p21 expression vector (pPSA-p21) showed that p21 does not reduce NKX3.1 expression, indicating that NKX3.1 expression is not the result of nonspecific effects of cell growth arrest. Our results provide biochemical and cellular biologic evidence that NKX3.1 is down-regulated by p53 over-expression in prostate cancer cells.

摘要

前列腺癌是一种涉及复杂多基因改变的疾病。NKX3.1和p53均与前列腺癌相关,并在前列腺癌进展中起关键作用。然而,关于p53与NKX3.1在前列腺癌中的关系及相互作用,人们所知甚少。我们发现,在前列腺癌LNCaP细胞中,野生型(wt)p53的过表达会下调NKX3.1的表达。由于外源性p53的瞬时转染或内源性p53的诱导,p53过表达会在mRNA和蛋白质水平下调NKX3.1。p53过表达通过抑制雄激素受体(AR)基因的启动子并阻断AR-DNA结合活性,抑制雄激素诱导的NKX3.1反式激活。此外,用p21表达载体(pPSA-p21)转染表明,p21不会降低NKX3.1的表达,这表明NKX3.1的表达不是细胞生长停滞非特异性效应的结果。我们的结果提供了生化和细胞生物学证据,表明在前列腺癌细胞中,p53过表达会下调NKX3.1的表达。

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