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针对癌症中的 Axl 和 Mer 激酶。

Targeting Axl and Mer kinases in cancer.

机构信息

Pediatric Hematology/Oncology, Primary Children's Medical Center, Huntsman Cancer Institute, 2000 Circle of Hope, Salt Lake City, UT 84112, USA.

出版信息

Mol Cancer Ther. 2011 Oct;10(10):1763-73. doi: 10.1158/1535-7163.MCT-11-0116. Epub 2011 Sep 20.

Abstract

Receptor tyrosine kinases (RTK) are cell-surface transmembrane receptors that contain regulated kinase activity within their cytoplasmic domain and play an important role in signal transduction in both normal and malignant cells. The mammalian TAM RTK family includes 3 closely related members: Tyro-3, Axl, and Mer. Overexpression or ectopic expression of the TAM receptors has been detected in a wide array of human cancers. Growth arrest-specific gene 6 has been identified as the major ligand for these TAM RTKs, and its binding to the receptors has been shown to promote proliferation and survival of cancer cells in vitro. Abnormal expression and activation of Axl or Mer can provide a survival advantage for certain cancer cells. Inhibition of Axl and Mer may enhance the sensitivity of cancer cells to cytotoxic agents and would potentially be a therapeutic strategy to target cancer cells. This review elucidates the role of Axl and Mer in normal cellular function and their role in oncogenesis. In addition, we review the potential to inhibit these RTKs for the development of therapeutic targets in treatment of cancer.

摘要

受体酪氨酸激酶(RTK)是细胞表面跨膜受体,其细胞质结构域内含有调节激酶活性,在正常和恶性细胞的信号转导中发挥重要作用。哺乳动物 TAM RTK 家族包括 3 个密切相关的成员:Tyro-3、Axl 和 Mer。在广泛的人类癌症中已检测到 TAM 受体的过表达或异位表达。生长停滞特异性基因 6 已被确定为这些 TAM RTK 的主要配体,其与受体的结合已被证明可促进体外癌细胞的增殖和存活。Axl 或 Mer 的异常表达和激活可为某些癌细胞提供生存优势。抑制 Axl 和 Mer 可能会提高癌细胞对细胞毒性药物的敏感性,并且可能成为靶向癌细胞的治疗策略。这篇综述阐明了 Axl 和 Mer 在正常细胞功能中的作用及其在肿瘤发生中的作用。此外,我们还回顾了抑制这些 RTK 以开发治疗癌症的治疗靶点的潜力。

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