Mokarram Pooneh, Albokashy Mohammed, Zarghooni Maryam, Moosavi Mohammad Amin, Sepehri Zahra, Chen Qi Min, Hudecki Andrzej, Sargazi Aliyeh, Alizadeh Javad, Moghadam Adel Rezaei, Hashemi Mohammad, Movassagh Hesam, Klonisch Thomas, Owji Ali Akbar, Łos Marek J, Ghavami Saeid
a Colorectal Research Center and Department of Biochemistry , School of Medicine, Shiraz University of Medical Sciences , Shiraz , Iran.
b Department of Human Anatomy and Cell Science , Rady Faculty of Health Sciences, Max Rady College of Medicine, University of Manitoba , Winnipeg , MB , Canada.
Autophagy. 2017 May 4;13(5):781-819. doi: 10.1080/15548627.2017.1290751. Epub 2017 Feb 23.
Colorectal cancer (CRC), despite numerous therapeutic and screening attempts, still remains a major life-threatening malignancy. CRC etiology entails both genetic and environmental factors. Macroautophagy/autophagy and the unfolded protein response (UPR) are fundamental mechanisms involved in the regulation of cellular responses to environmental and genetic stresses. Both pathways are interconnected and regulate cellular responses to apoptotic stimuli. In this review, we address the epidemiology and risk factors of CRC, including genetic mutations leading to the occurrence of the disease. Next, we discuss mutations of genes related to autophagy and the UPR in CRC. Then, we discuss how autophagy and the UPR are involved in the regulation of CRC and how they associate with obesity and inflammatory responses in CRC. Finally, we provide perspectives for the modulation of autophagy and the UPR as new therapeutic options for CRC treatment.
尽管进行了大量的治疗和筛查尝试,结直肠癌(CRC)仍然是一种主要的危及生命的恶性肿瘤。CRC的病因涉及遗传和环境因素。巨自噬/自噬和未折叠蛋白反应(UPR)是参与调节细胞对环境和遗传应激反应的基本机制。这两条途径相互关联,并调节细胞对凋亡刺激的反应。在本综述中,我们阐述了CRC的流行病学和危险因素,包括导致该疾病发生的基因突变。接下来,我们讨论CRC中与自噬和UPR相关的基因突变。然后,我们讨论自噬和UPR如何参与CRC的调节,以及它们如何与CRC中的肥胖和炎症反应相关联。最后,我们提供了调节自噬和UPR作为CRC治疗新选择的前景。