Wang Chun Yan, Guo Su Tang, Wang Jia Yu, Yan Xu Guang, Farrelly Margaret, Zhang Yuan Yuan, Liu Fen, Yari Hamed, La Ting, Lei Fu Xi, Jin Lei, Zhang Xu Dong, Jiang Chen Chen
School of Biomedical Sciences and Pharmacy, The University of Newcastle, NSW, Australia.
Department of Molecular Biology, Shanxi Cancer Hospital and Institute, Taiyuan, Shanxi, China.
Oncotarget. 2016 Aug 2;7(31):49597-49610. doi: 10.18632/oncotarget.10414.
Oncogenic mutations of BRAF occur in approximately 10% of colon cancers and are associated with their resistance to clinically available therapeutic drugs and poor prognosis of the patients. Here we report that colon cancer cells with mutant BRAF are also resistant to the heat shock protein 90 (HSP90) inhibitor AUY922, and that this is caused by rebound activation of ERK and Akt. Although AUY922 triggered rapid reduction in ERK and Akt activation in both wild-type and mutant BRAF colon cancer cells, activation of ERK and Akt rebounded shortly in the latter leading to resistance of the cells to AUY922-induced apoptosis. Reactivation of ERK was associated with the persistent expression of mutant BRAF, which, despite being a client of HSP90, was only partially degraded by AUY922, whereas reactivation of Akt was related to the activity of the HSP90 co-chaperone, cell division cycle 37 (CDC37), in that knockdown of CDC37 inhibited Akt reactivation in mutant colon cancer cells treated with AUY922. In support, as a HSP90 client protein, Akt was only diminished by AUY922 in wild-type but not mutant BRAF colon cancer cells. Collectively, these results reveal that reactivation of ERK and Akt associated respectively with the activity of mutant BRAF and CDC37 renders mutant BRAF colon cancer cells resistant to AUY922, with implications of co-targeting mutant BRAF and/or CDC37 and HSP90 in the treatment of mutant BRAF colon cancers.
BRAF的致癌突变约发生在10%的结肠癌中,与这些癌症对临床可用治疗药物的耐药性以及患者的不良预后相关。在此我们报告,具有BRAF突变的结肠癌细胞也对热休克蛋白90(HSP90)抑制剂AUY922耐药,这是由ERK和Akt的反弹激活所致。尽管AUY922在野生型和突变型BRAF结肠癌细胞中均引发了ERK和Akt激活的快速降低,但ERK和Akt的激活在后者中很快反弹,导致细胞对AUY922诱导的凋亡产生耐药。ERK的重新激活与突变型BRAF的持续表达相关,尽管突变型BRAF是HSP90的一个客户蛋白,但仅被AUY922部分降解,而Akt的重新激活与HSP90共伴侣细胞分裂周期37(CDC37)的活性有关,因为敲低CDC37可抑制用AUY922处理的突变型结肠癌细胞中Akt的重新激活。作为支持,作为HSP90客户蛋白,Akt仅在野生型而非突变型BRAF结肠癌细胞中被AUY922减少。总的来说,这些结果表明,分别与突变型BRAF和CDC37的活性相关的ERK和Akt的重新激活使突变型BRAF结肠癌细胞对AUY922产生耐药,这意味着在治疗突变型BRAF结肠癌时联合靶向突变型BRAF和/或CDC37以及HSP90。