Viswakarma Navin, Nair Rakesh Sathish, Sondarva Gautam, Das Subhasis, Ibrahimi Lucas, Chen Zhiyong, Sinha Subhash, Rana Basabi, Rana Ajay
Department of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, Chicago, IL 60612, USA.
Department of Cell and Molecular Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Oncotarget. 2017 May 16;8(20):33172-33184. doi: 10.18632/oncotarget.16566.
Mixed Lineage Kinase 3 (MLK3), also called as MAP3K11 is a tightly regulated MAP3K member but its cellular function is still not fully understood. Earlier we reported post-translational regulation of MLK3 by estrogen (E2) that inhibited the kinase activity and favored survival of ER+ breast cancer cells. Here we report that MLK3 is also transcriptionally downregulated by E2 in ER+ breast cancer cells. Publicly available data and in situ hybridization of human breast tumors showed significant down regulation of MLK3 transcripts in ER+ tumors. The basal level of MLK3 transcripts and protein in ER+ breast cancer cell lines were significantly lower, and the protein expression was further down regulated by E2 in a time-dependent manner. Analysis of the promoter of MLK3 revealed two ERE sites which were regulated by E2 in ER+ but not in ER- breast cancer cell lines. Both ERα and ERβ were able to bind to MLK3 promoter and recruit nuclear receptor co-repressors (NCoR, SMRT and LCoR), leading to down-regulation of MLK3 transcripts. Collectively these results suggest that recruitment of nuclear receptor co-repressor is a key feature of ligand-dependent transcriptional repression of MLK3 by ERs. Therefore coordinated transcriptional and post-translational repression of pro-apoptotic MLK3 probably is one of the mechanisms by which ER+ breast cancer cells proliferate and survive.
混合谱系激酶3(MLK3),也称为MAP3K11,是一种受到严格调控的丝裂原活化蛋白激酶3(MAP3K)成员,但其细胞功能仍未完全明确。此前我们报道过雌激素(E2)对MLK3的翻译后调控,这种调控抑制了激酶活性,并有利于雌激素受体阳性(ER+)乳腺癌细胞的存活。在此我们报道,在ER+乳腺癌细胞中,MLK3也会受到E2的转录下调。公开可得的数据以及人乳腺肿瘤的原位杂交显示,ER+肿瘤中MLK3转录本显著下调。ER+乳腺癌细胞系中MLK3转录本和蛋白的基础水平显著更低,并且蛋白表达会被E2以时间依赖性方式进一步下调。对MLK3启动子的分析揭示了两个雌激素反应元件(ERE)位点,它们在ER+乳腺癌细胞系中受E2调控,而在ER-乳腺癌细胞系中不受调控。雌激素受体α(ERα)和雌激素受体β(ERβ)均能够与MLK3启动子结合,并募集核受体共抑制因子(NCoR、SMRT和LCoR),从而导致MLK3转录本下调。总体而言,这些结果表明,募集核受体共抑制因子是雌激素受体对MLK3进行配体依赖性转录抑制的关键特征。因此,对促凋亡蛋白MLK3的转录和翻译后协同抑制可能是ER+乳腺癌细胞增殖和存活的机制之一。