Department of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai 200032, PR China.
Oncol Rep. 2012 Apr;27(4):917-22. doi: 10.3892/or.2011.1598. Epub 2011 Dec 20.
S100A4 protein, a member of the S100 superfamily of calcium-binding proteins, is frequently observed in various types of human cancers, including colorectal cancer (CRC). Our previous investigations have demonstrated that the overexpression of S100A4 is associated with lymph node metastasis and poor prognosis in CRC; however, its biological roles in CRC remain unclear. In the present study, we compared the expression of S100A4 at the mRNA and protein levels in six CRC cell lines, and found that the expression levels roughly coincided with their invasiveness. Using RNA interference, we suppressed S100A4 expression in SW620 CRC cells with highly invasive potential and S100A4 high expression. The specific knockdown of S100A4 strongly suppressed cell growth, migration and invasion activities. Furthermore, employing metastasis-related gene mRNA microarrays, we found four genes to be significantly dysregulated (more than 2-fold) after downregulation of S100A4, including three downregulated genes (MMP9, MMP10 and CDH11) and one upregulated gene (TIMP4). Our present results indicate that S100A4 may positively regulate tumor cell proliferation, invasion and metastasis associated with multiple molecules. Thus, the inhibition of S100A4 might be a potentially novel approach to treatment for CRC.
S100A4 蛋白是 S100 钙结合蛋白超家族的成员,在多种人类癌症中频繁出现,包括结直肠癌(CRC)。我们之前的研究表明,S100A4 的过表达与 CRC 的淋巴结转移和预后不良有关;然而,其在 CRC 中的生物学作用尚不清楚。在本研究中,我们比较了 6 种 CRC 细胞系中 S100A4 在 mRNA 和蛋白水平上的表达,发现其表达水平与侵袭性大致相符。通过 RNA 干扰,我们在具有高侵袭潜能和 S100A4 高表达的 SW620 CRC 细胞中抑制了 S100A4 的表达。S100A4 的特异性敲低强烈抑制了细胞的生长、迁移和侵袭活性。此外,通过转移相关基因 mRNA 微阵列,我们发现 S100A4 下调后有四个基因显著失调(超过 2 倍),包括三个下调基因(MMP9、MMP10 和 CDH11)和一个上调基因(TIMP4)。我们目前的结果表明,S100A4 可能通过多种分子正向调节肿瘤细胞的增殖、侵袭和转移。因此,抑制 S100A4 可能是一种治疗 CRC 的潜在新方法。