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Steroid Receptor Coactivator-3/AIB1 Promotes Cell Migration and Invasiveness through Focal Adhesion Turnover and Matrix Metalloproteinase Expression

机译:类固醇受体Coactivator-3 / AIB1通过局灶性粘着转变和基质金属蛋白酶表达促进细胞迁移和侵袭

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摘要

Steroid receptor coactivator-3 (SRC-3)/AIB1 is a member of the p160 nuclear receptor coactivator family involved in development and cell cycle progression. We previously showed that SRC-3/AIB1 is required for prostate cancer cell proliferation and survival. Here, we reported that the elevated SRC-3/AIB1 expression is significantly correlated with human prostate cancer seminal vesicle invasion and lymph node metastasis. Furthermore, SRC-3/AIB1 is associated with increased prostate cancer cell migration and invasion. SRC-3/AIB1 is required for focal adhesion turnover and focal adhesion kinase activation. In addition, SRC-3/AIB1 directly regulates transcription of matrix metalloproteinase (MMP)-2 and MMP-13 through its coactivation of AP-1 and PEA3. Taken together, these data suggest that SRC-3/AIB1 plays an essential role in prostate cancer cell invasion and metastasis.
机译:类固醇受体共激活因子3(SRC-3)/ AIB1是参与发育和细胞周期进程的p160核受体共激活因子家族的成员。我们以前表明,SRC-3 / AIB1是前列腺癌细胞增殖和生存所必需的。在这里,我们报道,升高的SRC-3 / AIB1表达与人类前列腺癌精囊侵袭和淋巴结转移显着相关。此外,SRC-3 / AIB1与前列腺癌细胞迁移和侵袭增加有关。 SRC-3 / AIB1是粘着斑更新和粘着斑激酶激活所必需的。此外,SRC-3 / AIB1通过对AP-1和PEA3的共激活直接调节基质金属蛋白酶(MMP)-2和MMP-13的转录。综上所述,这些数据表明SRC-3 / AIB1在前列腺癌细胞的侵袭和转移中起着至关重要的作用。

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