Pawar Jogendra Singh, Al-Amin Md Yusuf, Hu Chang-Deng
Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, IN, United States.
Purdue University Interdisciplinary Life Sciences Graduate Program, Purdue University, West Lafayette, IN, United States.
Front Oncol. 2023 Mar 7;13:1126482. doi: 10.3389/fonc.2023.1126482. eCollection 2023.
Radiation therapy (RT) is a standard treatment regimen for locally advanced prostate cancer; however, its failure results in tumor recurrence, metastasis, and cancer-related death. The recurrence of cancer after radiotherapy is one of the major challenges in prostate cancer treatment. Despite overall cure rate of 93.3% initially, prostate cancer relapse in 20-30% patients after radiation therapy. Cancer cells acquire radioresistance upon fractionated ionizing radiation (FIR) treatment, eventually undergo neuroendocrine differentiation (NED) and transform into neuroendocrine-like cells, a mechanism involved in acquiring resistance to radiation therapy. Radiosensitizers are agents that inhibit the repair of radiation-induced DNA damage. Protein arginine methyltransferase 5 (PRMT5) gets upregulated upon ionizing radiation treatment and epigenetically activates DNA damage repair genes in prostate cancer cells. In this study, we targeted PRMT5 with JNJ-64619178 and assessed its effect on DNA damage repair gene activation, radiosensitization, and FIR-induced NED in prostate cancer.
γH2AX foci analysis was performed to evaluate the DNA damage repair after radiation therapy. RT-qPCR and western blot were carried out to analyze the expression of DNA damage repair genes. Clonogenic assay was conducted to find out the surviving fraction after radiation therapy. NED was targeted with JNJ-64619178 in androgen receptor (AR) positive and negative prostate cancer cells undergoing FIR treatment.
JNJ-64619178 inhibits DNA damage repair in prostate cancer cells independent of their AR status. JNJ-64619178 impairs the repair of ionizing radiation-induced damaged DNA by transcriptionally inhibiting the DNA damage repair gene expression and radiosensitizes prostate, glioblastoma and lung cancer cell line. It targets NED induced by FIR in prostate cancer cells.
JNJ-64619178 can radiosensitize and suppress NED induced by FIR in prostate cancer cells and can be a potential radiosensitizer for prostate cancer treatment.
放射治疗(RT)是局部晚期前列腺癌的标准治疗方案;然而,其治疗失败会导致肿瘤复发、转移及癌症相关死亡。放射治疗后癌症复发是前列腺癌治疗中的主要挑战之一。尽管初始总体治愈率为93.3%,但20%至30%的患者在放射治疗后前列腺癌仍会复发。癌细胞在分次电离辐射(FIR)治疗后获得放射抗性,最终发生神经内分泌分化(NED)并转化为神经内分泌样细胞,这是一种与获得放射治疗抗性有关的机制。放射增敏剂是抑制辐射诱导的DNA损伤修复的药物。蛋白精氨酸甲基转移酶5(PRMT5)在电离辐射治疗后上调,并在表观遗传水平上激活前列腺癌细胞中的DNA损伤修复基因。在本研究中,我们用JNJ-64619178靶向PRMT5,并评估其对DNA损伤修复基因激活、放射增敏作用以及FIR诱导的前列腺癌NED的影响。
进行γH2AX焦点分析以评估放射治疗后的DNA损伤修复。开展RT-qPCR和蛋白质印迹法以分析DNA损伤修复基因的表达。进行克隆形成试验以确定放射治疗后的存活分数。在接受FIR治疗的雄激素受体(AR)阳性和阴性前列腺癌细胞中,用JNJ-64619178靶向NED。
JNJ-64619178抑制前列腺癌细胞中的DNA损伤修复,与它们的AR状态无关。JNJ-64619178通过转录抑制DNA损伤修复基因表达来损害电离辐射诱导的受损DNA的修复,并使前列腺癌、胶质母细胞瘤和肺癌细胞系对辐射增敏。它靶向前列腺癌细胞中FIR诱导的NED。
JNJ-64619178可使前列腺癌细胞对辐射增敏并抑制FIR诱导的NED,可能成为前列腺癌治疗的潜在放射增敏剂。