Department of General Surgery, Shanghai Jiaotong University Affiliated First People’s Hospital, Shanghai, People's Republic of China.
Exp Biol Med (Maywood). 2012 Oct;237(10):1231-40. doi: 10.1258/ebm.2012.011380. Epub 2012 Oct 26.
Piwi-like protein 2 (Piwil2) has recently emerged as a putative oncogene which is amplified in several human malignancies. However, the role of Piwil2 in colon cancer remains poorly understood. The aim of this study was to investigate the clinical and pathological significance of Piwil2, and the possible role in the proliferation and metastasis of colon cancer. Primary colon cancer paired with adjacent normal colon tissue and lymph node metastasis (LNM) lesions in 66 patients' tissue microarrays (TMA) were used to determine the expression of Piwil2. Knocked down Piwil2 expression in SW620 and SW480 colon cancer cell lines was performed to evaluate the role of Piwil2 in cell proliferation, invasion, metastasis in vitro and tumorigenicity in vivo. The possible roles of Piwil2 in the regulation of a 2 kb matrix metallopeptidase 9 (MMP9) promoter fragment and on the regulation of apoptotic pathways were evaluated by using a luciferase reporter construct and Western blots, respectively. Significantly higher expression levels of Piwil2 were observed in primary colon cancer tissue and in LNM in comparison with normal colon mucosa. Piwil2 expression significantly correlated with more aggressive clinical and pathological parameters with poorer five-year metastasis-free survival and overall survival. Piwil2 silencing significantly reduced cancer cell proliferation, colony formation ability and increased apoptosis in vitro and inhibited tumor growth in vivo. Piwil2 knockdown also attenuated migration and invasion of colon cancer cells via modulation of MMP9 transcriptional activities. Our results indicate that Piwil2 moderates the proliferation and metastasis potential of colon cancer.
Piwi 样蛋白 2(Piwil2)最近被认为是一种假定的癌基因,在几种人类恶性肿瘤中扩增。然而,Piwil2 在结肠癌中的作用仍知之甚少。本研究旨在探讨 Piwil2 的临床和病理意义,以及其在结肠癌增殖和转移中的可能作用。使用 66 例患者组织微阵列(TMA)中的原发性结肠癌配对的相邻正常结肠组织和淋巴结转移(LNM)病变来确定 Piwil2 的表达。在 SW620 和 SW480 结肠癌细胞系中敲低 Piwil2 表达,以评估 Piwil2 在体外细胞增殖、侵袭、转移和体内致瘤性中的作用。通过荧光素酶报告构建体和 Western blot 分别评估 Piwil2 在调节 2 kb 基质金属蛋白酶 9(MMP9)启动子片段和调节凋亡途径中的可能作用。与正常结肠黏膜相比,原发性结肠癌组织和 LNM 中观察到 Piwil2 的表达水平明显更高。Piwil2 表达与更具侵袭性的临床和病理参数显著相关,5 年无转移生存率和总生存率较差。Piwil2 沉默显著降低了体外癌细胞增殖、集落形成能力和增加了细胞凋亡,并抑制了体内肿瘤生长。Piwil2 敲低还通过调节 MMP9 转录活性减弱了结肠癌细胞的迁移和侵袭。我们的结果表明,Piwil2 调节结肠癌的增殖和转移潜力。