Department of Surgery and Cancer Biology, Loyola University Chicago Stritch School of Medicine, Maywood, IL.
Department of Public Health Sciences, Loyola University Chicago Stritch School of Medicine, Maywood, IL.
Hepatology. 2019 Nov;70(5):1631-1645. doi: 10.1002/hep.30707. Epub 2019 Jun 22.
There is an urgent need to understand the molecular signaling pathways that drive or mediate the development of hepatocellular carcinoma (HCC). The focal adhesion kinase (FAK) gene protein tyrosine kinase 2 is amplified in 16.4% of The Cancer Genome Atlas HCC specimens, and its amplification leads to increased FAK mRNA expression. It is not known whether the overexpression of FAK alone is sufficient to induce HCC or whether it must cooperate in some ways with other oncogenes. In this study, we found that 34.8% of human HCC samples with FAK amplification also show β-catenin mutations, suggesting a co-occurrence of FAK overexpression and β-catenin mutations in HCC. We overexpressed FAK alone, constitutively active forms of β-catenin (CAT) alone, or a combination of FAK and CAT in the livers of C57/BL6 mice. We found that overexpression of both FAK and CAT, but neither FAK nor CAT alone, in mouse livers was sufficient to lead to tumorigenesis. We further demonstrated that FAK's kinase activity is required for FAK/CAT-induced tumorigenesis. Furthermore, we performed RNA-sequencing analysis to identify the genes/signaling pathways regulated by FAK, CAT, or FAK/CAT. We found that FAK overexpression dramatically enhances binding of β-catenin to the promoter of androgen receptor (AR), which leads to increased expression of AR in mouse livers. Moreover, ASC-J9, an AR degradation enhancer, suppressed FAK/CAT-induced HCC formation. Conclusion: FAK overexpression and β-catenin mutations often co-occur in human HCC tissues. Co-overexpression of FAK and CAT leads to HCC formation in mice through increased expression of AR; this mouse model may be useful for further studies of the molecular mechanisms in the pathogenesis of HCC and could lead to the identification of therapeutic targets.
目前迫切需要了解驱动或介导肝细胞癌(HCC)发生的分子信号通路。焦点黏附激酶(FAK)基因蛋白酪氨酸激酶 2 在癌症基因组图谱(TCGA)HCC 标本中的扩增率为 16.4%,其扩增导致 FAK mRNA 表达增加。目前尚不清楚 FAK 的过表达是否足以单独诱导 HCC,还是它必须以某种方式与其他癌基因合作。在这项研究中,我们发现 FAK 扩增的 34.8%人类 HCC 样本也显示 β-连环蛋白突变,提示 HCC 中 FAK 过表达和 β-连环蛋白突变的共同发生。我们单独过表达 FAK、β-连环蛋白(CAT)的组成型激活形式(CAT)或 FAK 和 CAT 的组合在 C57/BL6 小鼠的肝脏中。我们发现,在小鼠肝脏中过表达 FAK 和 CAT,但单独过表达 FAK 或 CAT 均不足以导致肿瘤发生。我们进一步证明 FAK 的激酶活性是 FAK/CAT 诱导肿瘤发生所必需的。此外,我们进行了 RNA 测序分析,以鉴定受 FAK、CAT 或 FAK/CAT 调控的基因/信号通路。我们发现 FAK 过表达显著增强了 β-连环蛋白与雄激素受体(AR)启动子的结合,导致 AR 在小鼠肝脏中的表达增加。此外,AR 降解增强剂 ASC-J9 抑制了 FAK/CAT 诱导的 HCC 形成。结论:FAK 过表达和 β-连环蛋白突变通常在人类 HCC 组织中共同发生。FAK 和 CAT 的共过表达通过增加 AR 的表达导致小鼠 HCC 的形成;这种小鼠模型可能有助于进一步研究 HCC 发病机制中的分子机制,并可能导致治疗靶点的鉴定。