Centre for Biodiscovery and Molecular Development of Therapeutics, James Cook University, Townsville, QLD, 4811, Australia.
Research Institute in Oncology and Hematology, CancerCare Manitoba, Winnipeg, MB, Canada.
Apoptosis. 2018 Feb;23(2):93-112. doi: 10.1007/s10495-018-1440-4.
Cancer is a primary cause of human fatality and conventional cancer therapies, e.g., chemotherapy, are often associated with adverse side-effects, tumor drug-resistance, and recurrence. Molecularly targeted therapy, composed of small-molecule inhibitors and immunotherapy (e.g., monoclonal antibody and cancer vaccines), is a less harmful alternative being more effective against cancer cells whilst preserving healthy tissues. Drug-resistance, however, caused by negative regulation of cell death signaling pathways, is still a challenge. Circumvention of negative regulators of cell death pathways or development of predictive and response biomarkers is, therefore, quintessential. This review critically discusses the current state of knowledge on targeting negative regulators of cell death signaling pathways including apoptosis, ferroptosis, necroptosis, autophagy, and anoikis and evaluates the recent advances in clinical and preclinical research on biomarkers of negative regulators. It aims to provide a comprehensive platform for designing efficacious polytherapies including novel agents for restoring cell death signaling pathways or targeting alternative resistance pathways to improve the chances for antitumor responses. Overall, it is concluded that nonapoptotic cell death pathways are a potential research arena for drug discovery, development of novel biomarkers and targeted therapies.
癌症是人类死亡的主要原因,传统的癌症疗法,如化疗,常伴有不良反应、肿瘤耐药和复发。由小分子抑制剂和免疫疗法(如单克隆抗体和癌症疫苗)组成的分子靶向治疗是一种危害较小的替代方法,对癌细胞更有效,同时保护健康组织。然而,细胞死亡信号通路的负调控导致的耐药性仍然是一个挑战。因此,回避细胞死亡信号通路的负调节剂或开发预测和反应生物标志物至关重要。本综述批判性地讨论了靶向细胞死亡信号通路负调节剂的最新研究进展,包括细胞凋亡、铁死亡、坏死性凋亡、自噬和细胞凋亡,并评估了关于负调节剂生物标志物的临床前和临床研究的最新进展。它旨在为设计有效的多疗法提供一个综合平台,包括恢复细胞死亡信号通路的新药物或靶向替代耐药途径,以提高抗肿瘤反应的机会。总的来说,非凋亡细胞死亡途径是药物发现、新型生物标志物和靶向治疗开发的一个潜在研究领域。