Dadakhujaev Shorafidinkhuja, Salazar-Arcila Carolina, Netherton Stuart J, Chandhoke Amrita Singh, Singla Arvind Kumar, Jirik Frank R, Bonni Shirin
Department of Biochemistry and Molecular Biology, University of Calgary, Calgary, Alberta, Canada ; Southern Alberta Cancer Research Institute, University of Calgary, Calgary, Alberta, Canada.
Department of Biochemistry and Molecular Biology, University of Calgary, Calgary, Alberta, Canada ; McCaig Institute for Bone and Joint Health, University of Calgary, Calgary, Alberta, Canada.
Oncoscience. 2014 Mar 31;1(3):229-40. doi: 10.18632/oncoscience.27. eCollection 2014.
Tumor metastasis contributes to the grave morbidity and mortality of cancer, but the mechanisms underlying tumor cell invasiveness and metastasis remain incompletely understood. Here, we report that expression of the SUMO E3 ligase PIAS1 suppresses TGFβ-induced activation of the matrix metalloproteinase MMP2 in human breast cancer cells. We also find that knockdown of endogenous PIAS1 or inhibition of its SUMO E3 ligase activity stimulates the ability of TGFβ to induce an aggressive phenotype in three-dimensional breast cancer cell organoids. Importantly, inhibition of the SUMO E3-ligase activity of PIAS1 in breast cancer cells promotes metastases in mice in vivo. Collectively, our findings define a novel and critical role for the SUMO E3 ligase PIAS1 in the regulation of the invasive and metastatic potential of malignant breast cancer cells. These findings advance our understanding of cancer invasiveness and metastasis with potential implications for the development of biomarkers and therapies in breast cancer.
肿瘤转移导致癌症严重的发病率和死亡率,但其潜在机制仍未完全明确。在此,我们报道小泛素样修饰蛋白E3连接酶PIAS1的表达抑制人乳腺癌细胞中转化生长因子β(TGFβ)诱导的基质金属蛋白酶MMP2的激活。我们还发现,敲低内源性PIAS1或抑制其小泛素样修饰蛋白E3连接酶活性,会增强TGFβ在三维乳腺癌细胞类器官中诱导侵袭性表型的能力。重要的是,抑制乳腺癌细胞中PIAS1的小泛素样修饰蛋白E3连接酶活性,可促进小鼠体内的转移。总之,我们的研究结果确定了小泛素样修饰蛋白E3连接酶PIAS1在调节恶性乳腺癌细胞侵袭和转移潜能方面的新的关键作用。这些发现加深了我们对癌症侵袭和转移的理解,对乳腺癌生物标志物和治疗方法的开发具有潜在意义。