Laboratory of Digestive Surgery, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan Province, China.
Mol Biol Rep. 2012 Jan;39(1):243-9. doi: 10.1007/s11033-011-0732-3. Epub 2011 May 10.
PNAS-4 is a novel pro-apoptotic protein activated during the early response to DNA damage; however, the molecular mechanisms and pathways regulating PNAS-4 expression in tumors are not well understood. We hypothesized that PNAS-4 is a p53 down-stream target gene and designed this study. We searched online for putative p53-binding sites in the entire PNAS-4 gene and did not find any corresponding information. In HCT116 colon cancer cells, after being transfected with small interfering RNA to silence p53, the expressions of PNAS-4 and other known p53 target gene (Apaf1, Bax, Fas and Dr5) were determined by real-time PCR. We found that PNAS-4 was up-regulated while Apaf1, Bax, Fas and Dr5 were down-regulated. We then examined the expression of PNAS-4 and p53 mutation in colorectal cancer patients. PNAS-4 expressed both in colorectal cancers and normal tissues, but compared with paired control, PNAS-4 was up-regulated in cancers (P=0.018). PNAS-4 overexpression ratios were correlated to the p53 mutant status (P=0.001). The mean PNAS-4 expression levels of p53 mutant homozygote group and heterozygote group were higher than that of p53 wild type group (P=0.013). The expression ratios of PNAS-4 (every sample in relative to its paired normal mucosa) were different between negative lymph node metastasis (66% up-regulated, 34% down-regulated) and positive metastasis (42% up-regulated, 58% down-regulated). Taken together, these findings suggested that PNAS-4 was not a p53 target, but overexpression of PNAS-4 was correlated to p53 inactivity in colorectal cancer.
PNAS-4 是一种新型的促凋亡蛋白,在 DNA 损伤早期反应中被激活;然而,调节肿瘤中 PNAS-4 表达的分子机制和途径尚不清楚。我们假设 PNAS-4 是 p53 的下游靶基因,并设计了这项研究。我们在线搜索了 PNAS-4 基因中所有可能的 p53 结合位点,但没有找到任何相关信息。在 HCT116 结肠癌细胞中,用小干扰 RNA 转染沉默 p53 后,通过实时 PCR 测定 PNAS-4 和其他已知的 p53 靶基因(Apaf1、Bax、Fas 和 Dr5)的表达。我们发现 PNAS-4 上调,而 Apaf1、Bax、Fas 和 Dr5 下调。然后,我们检测了结直肠癌患者的 PNAS-4 表达和 p53 突变。PNAS-4 在结直肠癌和正常组织中均有表达,但与配对对照相比,PNAS-4 在癌症中上调(P=0.018)。PNAS-4 过表达比率与 p53 突变状态相关(P=0.001)。p53 突变纯合子组和杂合子组的 PNAS-4 平均表达水平均高于 p53 野生型组(P=0.013)。p53 突变阴性淋巴结转移(66%上调,34%下调)和阳性转移(42%上调,58%下调)之间,PNAS-4(每个样本与其配对的正常粘膜相比)的表达比率不同。综上所述,这些发现表明 PNAS-4 不是 p53 的靶基因,但 PNAS-4 的过度表达与结直肠癌中 p53 失活相关。