Liang Yulong, Yu Lihou, Zhang Dongxiao, Zhao Xuemei, Gao Hong, Slagle Betty L, Goss John A, Wang Xiaosong, Li Kaiyi, Lin Shiaw-Yih
The Michael E. DeBakey Department of Surgery, Baylor College of Medicine Houston, TX, USA.
Beijing Hospital of Traditional Chinese Medicine, Capital Medical University Beijing, China.
Am J Cancer Res. 2020 Jun 1;10(6):1900-1918. eCollection 2020.
BRIT1 has emerged as a novel key player in homologous recombination (HR). It is located in 8p23, a locus frequently deleted in hepatocellular carcinoma (HCC). Previously, we found that BRIT1-deficiency triggered genomic instability and tumor formation in our mouse model. Here we aim to determine whether BRIT1 aberrations are implicated in HCC and, if so, whether they can be used for targeted therapy with PARP inhibitors and other agents. We analyzed HCC samples for BRIT1 alterations at DNA, RNA and protein levels. BRIT1 was found deleted and/or downregulated in ~30% of HCC samples; BRIT1 mutant K659fsX10 identified in HCC abolished DNA repair function. Notably, BRIT1 deletion was correlated with poor survival and high recurrence of HCC. To determine the role of BRIT1 deficiency in potentiating the drug response, we subsequently generated BRIT1-deficient HCC cells, determined their HR defects, and assessed their response to the PARPi olaparib and PI3K inhibitor in vitro and in mice. BRIT1-deficient HCC cells were HR defective and hypersensitive to olaparib alone or in combination with PI3K inhibitor BEZ235, both in vitro and in vivo. The cytotoxicity of olaparib alone or in combination with BEZ235 was largely alleviated by ectopic BRIT1. We also found that BEZ235 markedly enhanced the production of poly (ADP-ribose) and the level of double-strand breaks (DSB) and single-strand breaks (SSB) in BRIT1-deficient cells. In summary, our results identify BRIT1 deficiency as a potential driver for HCC development, and BRIT1 status is critical to sensitivity to treatment with olaparib and/or BEZ235. PI3K inhibition induces substantial DNA damage and makes cells more dependent on PARP activity in the context of BRIT1 deficiency, thus, BRIT1 depletion facilitates enhancing synthetic lethality of PARP inhibitors and PI3K inhibitors in HCC. This study provides a new mechanistic foundation for significantly expanding the application of PARPi in HCC therapy.
BRIT1已成为同源重组(HR)中的一个新的关键因子。它位于8p23,这是一个在肝细胞癌(HCC)中经常缺失的基因座。此前,我们发现在我们的小鼠模型中,BRIT1缺陷会引发基因组不稳定和肿瘤形成。在此,我们旨在确定BRIT1异常是否与HCC有关,如果有关,它们是否可用于PARP抑制剂和其他药物的靶向治疗。我们在DNA、RNA和蛋白质水平分析了HCC样本中的BRIT1改变。在约30%的HCC样本中发现BRIT1缺失和/或下调;在HCC中鉴定出的BRIT1突变体K659fsX10消除了DNA修复功能。值得注意的是,BRIT1缺失与HCC的不良生存和高复发率相关。为了确定BRIT1缺陷在增强药物反应中的作用,我们随后生成了BRIT1缺陷的HCC细胞,确定了它们的HR缺陷,并在体外和小鼠体内评估了它们对PARPi奥拉帕利和PI3K抑制剂的反应。BRIT1缺陷的HCC细胞在体外和体内均存在HR缺陷,并且对单独使用奥拉帕利或与PI3K抑制剂BEZ235联合使用均高度敏感。异位表达BRIT1可在很大程度上减轻单独使用奥拉帕利或与BEZ235联合使用时的细胞毒性。我们还发现,BEZ235显著增强了BRIT1缺陷细胞中聚(ADP-核糖)的产生以及双链断裂(DSB)和单链断裂(SSB)的水平。总之,我们的结果表明BRIT1缺陷是HCC发展的一个潜在驱动因素,并且BRIT1状态对于对奥拉帕利和/或BEZ235治疗的敏感性至关重要。在BRIT1缺陷的情况下,PI3K抑制会诱导大量DNA损伤并使细胞更依赖PARP活性,因此,BRIT1缺失有助于增强PARP抑制剂和PI3K抑制剂在HCC中的合成致死性。这项研究为显著扩大PARPi在HCC治疗中的应用提供了新的机制基础。