Zou Wei, Yang Hong, Hou Xianghua, Zhang Wei, Chen Biliang, Xin Xiaoyan
Department of Obstetrics and Gynecology, Xijing Hospital, The Fourth Military Medical University, Xi'an, PR China.
Cancer Lett. 2007 Apr 18;248(2):211-8. doi: 10.1016/j.canlet.2006.07.005. Epub 2006 Aug 22.
Overexpression of extracellular matrix metalloproteinase inducer (EMMPRIN or CD147), a member of the immunoglobulin family and a glycoprotein enriched on the surface of tumor cells, promotes invasion, metastasis, growth and survival of malignant cells, and confers resistance to some chemotherapeutic drugs. Here, we used a human U6 promoter-driven DNA template approach to induce short hairpin RNA (shRNA)-triggered RNA interference (RNAi) to block CD147 gene expression in the human ovarian cancer cell line HO-8910pm. Knockdown of CD147 by shRNA resulted in decrease of the HO-8910pm invasion activity in vitro and tumorigenicity in nude mice. The suppression of CD147 expression also sensitized cells to be more sensitive to paclitaxel. These results suggested that CD147 was an ovarian cancer-related gene and CD147 might be a potential target for therapeutic anti-cancer drugs.
细胞外基质金属蛋白酶诱导剂(EMMPRIN 或 CD147)是免疫球蛋白家族的成员,是一种富集于肿瘤细胞表面的糖蛋白,其过表达可促进恶性细胞的侵袭、转移、生长和存活,并赋予对某些化疗药物的抗性。在此,我们使用人 U6 启动子驱动的 DNA 模板方法来诱导短发夹 RNA(shRNA)触发的 RNA 干扰(RNAi),以阻断人卵巢癌细胞系 HO-8910pm 中的 CD147 基因表达。shRNA 敲低 CD147 导致 HO-8910pm 体外侵袭活性降低以及裸鼠体内致瘤性降低。CD147 表达的抑制还使细胞对紫杉醇更敏感。这些结果表明,CD147 是一个与卵巢癌相关的基因,并且 CD147 可能是治疗性抗癌药物的潜在靶点。