4.8 Article

Steroid receptor coactivator-3/AIB1 promotes cell migration and invasiveness through focal adhesion turnover and matrix metalloproteinase expression

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CANCER RESEARCH
卷 68, 期 13, 页码 5460-5468

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AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-08-0955

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  1. NCI NIH HHS [P50 CA058204-050012, P50 CA058204-080012, P50 CA058204-07S10012, P50 CA058204-070012, U01 CA105352, P50 CA058204, U01CA105352, P50 CA058204-090018, P50 CA058204-060012] Funding Source: Medline
  2. NIDDK NIH HHS [P01 DK059820-020001, R01 DK062821-03S1, DK 62821, R01 DK062821-01, P01 DK059820-050001, P01 DK059820-040001, P01 DK059820, R01 DK062821-04, P01 DK059820-010001, R01 DK062821-03, P01 DK059820-030001, R01 DK062821, R01 DK062821-02] Funding Source: Medline

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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.

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