Roles of partitioning‐defective protein 6 (Par6) and its complexes in the proliferation, migration and invasion of cancer cells

转移 癌症 生物 细胞生长 癌症研究 蛋白激酶A 激酶 细胞生物学 信号转导 生物化学 遗传学
作者
Ling‐Ling Ruan,Yanting Shen,Ziwen Lu,Dongsheng Shang,Zhicong Zhao,Yongjin Lu,Yanfang Wu,Yafei Zhang,Zhigang Tu,Hanqing Liu
出处
期刊:Clinical and Experimental Pharmacology and Physiology [Wiley]
卷期号:44 (9): 909-913 被引量:13
标识
DOI:10.1111/1440-1681.12794
摘要

Summary A pivotal regulator of cell polarity and homeostasis, partitioning‐defective protein 6 (Par6) forms multicomponent complexes that not only regulate cell polarity and stabilize cell morphology, but have also been demonstrated to participate in the proliferation, migration and invasion of cancer cells. The transforming growth factor ( TGF )‐β and extracellular signal‐regulated kinase (Erk) 1/2 pathways are the most thoroughly studied pathways involving Par6 in many cancers. Aurothiomalate has been used to disrupt the interaction between Par6 and atypical protein kinase C within the multicomponent complexes, and has been shown to effectively block transformed growth and metastasis in vitro and/or in vivo in a variety of cancers, including pancreatic, prostate and lung cancers, as well as alveolar rhabdomyosarcoma. It is likely that with further revelations regarding the critical roles of Par6 in cancer initiation, progression and metastasis, targeted therapies against Par6 will be discovered and prove effective preclinically, and hopefully clinically, in cancer treatment.

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