Blanco F F, Jimbo M, Wulfkuhle J, Gallagher I, Deng J, Enyenihi L, Meisner-Kober N, Londin E, Rigoutsos I, Sawicki J A, Risbud M V, Witkiewicz A K, McCue P A, Jiang W, Rui H, Yeo C J, Petricoin E, Winter J M, Brody J R
Department of Pharmacology and Experimental Therapeutics, Division of Clinical Pharmacology, Thomas Jefferson University, Philadelphia, PA, USA.
Department of Surgery, Thomas Jefferson University, Philadelphia, PA, USA.
Oncogene. 2016 May;35(19):2529-41. doi: 10.1038/onc.2015.325. Epub 2015 Sep 21.
Previously, it has been shown that pancreatic ductal adenocarcinoma (PDA) tumors exhibit high levels of hypoxia, characterized by low oxygen pressure (pO2) and decreased O2 intracellular perfusion. Chronic hypoxia is strongly associated with resistance to cytotoxic chemotherapy and chemoradiation in an understudied phenomenon known as hypoxia-induced chemoresistance. The hypoxia-inducible, pro-oncogenic, serine-threonine kinase PIM1 (Proviral Integration site for Moloney murine leukemia virus 1) has emerged as a key regulator of hypoxia-induced chemoresistance in PDA and other cancers. Although its role in therapeutic resistance has been described previously, the molecular mechanism behind PIM1 overexpression in PDA is unknown. Here, we demonstrate that cis-acting AU-rich elements (ARE) present within a 38-base pair region of the PIM1 mRNA 3'-untranslated region mediate a regulatory interaction with the mRNA stability factor HuR (Hu antigen R) in the context of tumor hypoxia. Predominantly expressed in the nucleus in PDA cells, HuR translocates to the cytoplasm in response to hypoxic stress and stabilizes the PIM1 mRNA transcript, resulting in PIM1 protein overexpression. A reverse-phase protein array revealed that HuR-mediated regulation of PIM1 protects cells from hypoxic stress through phosphorylation and inactivation of the apoptotic effector BAD and activation of MEK1/2. Importantly, pharmacological inhibition of HuR by MS-444 inhibits HuR homodimerization and its cytoplasmic translocation, abrogates hypoxia-induced PIM1 overexpression and markedly enhances PDA cell sensitivity to oxaliplatin and 5-fluorouracil under physiologic low oxygen conditions. Taken together, these results support the notion that HuR has prosurvival properties in PDA cells by enabling them with growth advantages in stressful tumor microenvironment niches. Accordingly, these studies provide evidence that therapeutic disruption of HuR's regulation of PIM1 may be a key strategy in breaking an elusive chemotherapeutic resistance mechanism acquired by PDA cells that reside in hypoxic PDA microenvironments.
此前的研究表明,胰腺导管腺癌(PDA)肿瘤呈现出高水平的缺氧状态,其特征为低氧分压(pO2)和细胞内氧灌注减少。慢性缺氧与细胞毒性化疗和放化疗耐药性密切相关,这一尚未得到充分研究的现象被称为缺氧诱导的化疗耐药性。缺氧诱导的、促癌的丝氨酸 - 苏氨酸激酶PIM1(莫洛尼鼠白血病病毒1的原病毒整合位点)已成为PDA和其他癌症中缺氧诱导化疗耐药性的关键调节因子。尽管其在治疗耐药性中的作用此前已有描述,但PDA中PIM1过表达背后的分子机制尚不清楚。在此,我们证明,PIM1 mRNA 3'非翻译区38个碱基对区域内存在的顺式作用富含AU元件(ARE)在肿瘤缺氧的情况下介导了与mRNA稳定性因子HuR(Hu抗原R)的调节相互作用。HuR在PDA细胞中主要在细胞核中表达,在缺氧应激下易位至细胞质并稳定PIM1 mRNA转录本,导致PIM1蛋白过表达。反相蛋白质阵列显示,HuR介导的PIM1调节通过凋亡效应因子BAD的磷酸化和失活以及MEK1/2的激活保护细胞免受缺氧应激。重要的是,MS - 444对HuR的药理抑制作用可抑制HuR同源二聚化及其细胞质易位,消除缺氧诱导的PIM1过表达,并在生理低氧条件下显著增强PDA细胞对奥沙利铂和5 - 氟尿嘧啶的敏感性。综上所述,这些结果支持了这样一种观点,即HuR通过使PDA细胞在应激性肿瘤微环境龛中具有生长优势而具有促生存特性。因此,这些研究提供了证据,表明治疗性破坏HuR对PIM1的调节可能是打破PDA细胞在缺氧的PDA微环境中获得的难以捉摸的化疗耐药机制的关键策略。