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Angiomotin family members: Oncogenes or tumor suppressors?

  • Meng Lv
  • , Yanwei Shen
  • , Jiao Yang
  • , Shuting Li
  • , Biyuan Wang
  • , Zheling Chen
  • , Pan Li
  • , Peijun Liu
  • , Jin Yang
  • The First Affiliated Hospital of Xi’an Jiaotong University

科研成果: 期刊稿件文献综述同行评审

62 引用 (Scopus)

摘要

Angiomotin (Amot) family contains three members: Amot (p80 and p130 isoforms), Amot-like protein 1 (Amotl1), and Amot-like protein 2 (Amotl2). Amot proteins play an important role in tube formation and migration of endothelial cells and the regulation of tight junctions, polarity, and epithelial-mesenchymal transition in epithelial cells. Moreover, these proteins regulate the proliferation and migration of cancer cells. In most cancers, Amot family members promote the proliferation and invasion of cancer cells, including breast cancer, osteosarcoma, colon cancer, prostate cancer, head and neck squamous cell carcinoma, cervical cancer, liver cancer, and renal cell cancer. However, in glioblastoma, ovarian cancer, and lung cancer, Amot inhibits the growth of cancer cells. In addition, there are controversies on the regulation of Yes-associated protein (YAP) by Amot. Amot promotes either the internalization of YAP into the nucleus or the retention of YAP in the cytoplasm of different cell types. Moreover, Amot regulates the AMPK, mTOR, Wnt, and MAPK signaling pathways. However, it is unclear whether Amot is an oncogene or a tumor suppressor gene in different cellular processes. This review focuses on the multifunctional roles of Amot in cancers.

源语言英语
页(从-至)772-781
页数10
期刊International Journal of Biological Sciences
13
6
DOI
出版状态已出版 - 2017
已对外发布

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