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组蛋白去乙酰化酶抑制剂对TRAIL/Apo2L凋亡途径的表观遗传调控:一种绕过黑色素瘤免疫治疗耐药性的有吸引力的方法。

Epigenetic regulation of the TRAIL/Apo2L apoptotic pathway by histone deacetylase inhibitors: an attractive approach to bypass melanoma immunotherapy resistance.

作者信息

Jazirehi Ali R, Arle Dylan

机构信息

Department of Surgery, Division of Surgical Oncology, and the Jonsson Comprehensive Cancer Center, David Geffen School of Medicine at UCLA, University of California at Los Angeles Los Angeles, California 90095.

出版信息

Am J Clin Exp Immunol. 2013 Feb 27;2(1):55-74. Print 2013.

Abstract

TNF-related apoptosis-inducing ligand (TRAIL/Apo2L) is a major cytotoxic mechanism employed by cytotoxic T lymphocytes (CTL) and natural killer (NK) cells to eradicate malignant cells. TRAIL/Apo2L interacts with its cognate receptors located on tumor cell surface namely, TRAIL-R1 (DR4), TRAIL-R2 (DR5), TRAIL-R3 (DcR1), TRAIL-R4 (DcR2) and osteoprotegerin (OPG). The exact function of DcR1 and DcR2 remains elusive. TRAIL/Apo2L or agonistic monoclonal antibodies directed against TRAIL/Apo2L death-inducing receptors (DR4, DR5) have become an attractive immunological therapeutic tools in clinical oncology due to their selective killing of tumors and lack of affinity towards healthy cells. Though a potent anti-cancer modality, some cancer cells exhibit inherent or acquired resistance to TRAIL/Apo2L. Postulated resistance mechanisms include up-regulation of c-FLIP, down-regulation of caspase-8, down-regulation/shedding of death receptors and an imbalanced ratio of pro- to anti-apoptotic genes due to aberrant activity of cellular survival signal transduction pathways. The development of resistance has spurred the use of combination therapy, in particular using small molecule sensitizing agents, to restore apoptosis sensitivity. A novel category of such compounds is histone deacetylase inhibitors (HDACi), which block HDACs from removing acetyl groups from histone tails thereby preventing silencing of pro-apoptotic genes and regulating the expression of non-histone proteins (i.e., apoptosis-associated genes), are effective agents in some malignancies. Some HDACi, such as Suberoylanilide Hydroxamic Acid (SAHA), have received FDA approval for cancer treatment. In various melanoma preclinical models, HDACi in conjunction with TRAIL/Apo2L, via modulation of apoptotic machinery, have proven to overcome acquired/inherent resistance to either agent. Here, we discuss recent findings on the role of TRAIL/Apo2L and its agonistic mAbs in melanoma immunotherapy with discussions on potential cellular and molecular events by which HDACi can sensitize metastatic melanoma to TRAIL/Apo2L-mediated immune-therapy, thereby, overcoming resistance.

摘要

肿瘤坏死因子相关凋亡诱导配体(TRAIL/Apo2L)是细胞毒性T淋巴细胞(CTL)和自然杀伤(NK)细胞用于根除恶性细胞的主要细胞毒性机制。TRAIL/Apo2L与其位于肿瘤细胞表面的同源受体相互作用,即TRAIL-R1(DR4)、TRAIL-R2(DR5)、TRAIL-R3(DcR1)、TRAIL-R4(DcR2)和骨保护素(OPG)。DcR1和DcR2的确切功能仍不清楚。TRAIL/Apo2L或针对TRAIL/Apo2L死亡诱导受体(DR4、DR5)的激动性单克隆抗体,由于它们对肿瘤的选择性杀伤以及对健康细胞缺乏亲和力,已成为临床肿瘤学中一种有吸引力的免疫治疗工具。尽管是一种有效的抗癌方式,但一些癌细胞对TRAIL/Apo2L表现出固有或获得性抗性。推测的抗性机制包括c-FLIP上调、半胱天冬酶-8下调、死亡受体下调/脱落以及由于细胞存活信号转导通路异常激活导致的促凋亡基因与抗凋亡基因比例失衡。抗性的产生促使了联合治疗的使用,特别是使用小分子增敏剂来恢复凋亡敏感性。这类化合物的一个新类别是组蛋白去乙酰化酶抑制剂(HDACi),它阻止HDAC从组蛋白尾部去除乙酰基,从而防止促凋亡基因沉默并调节非组蛋白(即凋亡相关基因)的表达,在某些恶性肿瘤中是有效的药物。一些HDACi,如辛二酰苯胺异羟肟酸(SAHA),已获得美国食品药品监督管理局(FDA)的癌症治疗批准。在各种黑色素瘤临床前模型中,HDACi与TRAIL/Apo2L联合使用,通过调节凋亡机制,已证明可克服对这两种药物的获得性/固有抗性。在此,我们讨论关于TRAIL/Apo2L及其激动性单克隆抗体在黑色素瘤免疫治疗中的作用的最新发现,并讨论HDACi使转移性黑色素瘤对TRAIL/Apo2L介导的免疫治疗敏感从而克服抗性的潜在细胞和分子事件。

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