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表观遗传去抑制使PPARγ成为三阴性和内分泌抵抗性乳腺癌中的一个可成药靶点。

Epigenetic derepression converts PPARγ into a druggable target in triple-negative and endocrine-resistant breast cancers.

作者信息

Loo Ser Yue, Syn Nicholas L, Koh Angele Pei-Fern, Teng Janet Cheng-Fei, Deivasigamani Amudha, Tan Tuan Zea, Thike Aye Aye, Vali Shireen, Kapoor Shweta, Wang Xiaoyuan, Wang Jiong Wei, Tan Puay Hoon, Yip George W, Sethi Gautam, Huang Ruby Yun-Ju, Hui Kam Man, Wang Lingzhi, Goh Boon Cher, Kumar Alan Prem

机构信息

Cancer Science Institute of Singapore and Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.

Genome Institute of Singapore, A*STAR, Singapore, Singapore.

出版信息

Cell Death Discov. 2021 Sep 27;7(1):265. doi: 10.1038/s41420-021-00635-5.

Abstract

Clinical trials repurposing peroxisome proliferator-activated receptor-gamma (PPARγ) agonists as anticancer agents have exhibited lackluster efficacy across a variety of tumor types. Here, we report that increased PPARG expression is associated with a better prognosis but is anticorrelated with histone deacetylase (HDAC) 1 and 2 expressions. We show that HDAC overexpression blunts anti-proliferative and anti-angiogenic responses to PPARγ agonists via transcriptional and post-translational mechanisms, however, these can be neutralized with clinically approved and experimental HDAC inhibitors. Supporting this notion, concomitant treatment with HDAC inhibitors was required to license the tumor-suppressive effects of PPARγ agonists in triple-negative and endocrine-refractory breast cancer cells, and combination therapy also restrained angiogenesis in a tube formation assay. This combination was also synergistic in estrogen receptor-alpha (ERα)-positive cells because HDAC blockade abrogated ERα interference with PPARγ-regulated transcription. Following a pharmacokinetics optimization study, the combination of rosiglitazone and a potent pan-HDAC inhibitor, LBH589, stalled disease progression in a mouse model of triple-negative breast cancer greater than either of the monotherapies, while exhibiting a favorable safety profile. Our findings account for historical observations of de-novo resistance to PPARγ agonist monotherapy and propound a therapeutically cogent intervention against two aggressive breast cancer subtypes.

摘要

将过氧化物酶体增殖物激活受体γ(PPARγ)激动剂重新用作抗癌药物的临床试验在多种肿瘤类型中疗效不佳。在此,我们报告PPARG表达增加与较好的预后相关,但与组蛋白去乙酰化酶(HDAC)1和2的表达呈负相关。我们发现HDAC过表达通过转录和翻译后机制减弱了对PPARγ激动剂的抗增殖和抗血管生成反应,然而,这些反应可以被临床批准的和实验性的HDAC抑制剂中和。支持这一观点的是,需要与HDAC抑制剂联合治疗才能使PPARγ激动剂在三阴性和内分泌难治性乳腺癌细胞中发挥肿瘤抑制作用,并且联合治疗在管形成试验中也抑制了血管生成。这种联合在雌激素受体α(ERα)阳性细胞中也具有协同作用,因为HDAC阻断消除了ERα对PPARγ调节转录的干扰。经过药代动力学优化研究后,罗格列酮与一种强效泛HDAC抑制剂LBH589的联合使用在三阴性乳腺癌小鼠模型中比任何一种单一疗法都更能延缓疾病进展,同时显示出良好的安全性。我们的研究结果解释了对PPARγ激动剂单一疗法的原发性耐药的历史观察结果,并提出了一种针对两种侵袭性乳腺癌亚型的有治疗说服力的干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c5d/8476547/1bad5fcf9282/41420_2021_635_Fig1_HTML.jpg

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