Yadav Raj Kumar, Chae Soo-Wan, Kim Hyung-Ryong, Chae Han Jung
Department of Pharmacology and Institute of Cardiovascular Research, School of Medicine, Chonbuk National University, Jeonju, Chonbuk, Korea.
Department of Dental Pharmacology, College of Dentistry, Wonkwang University, Iksan, Chonbuk, Korea.
J Cancer Prev. 2014 Jun;19(2):75-88. doi: 10.15430/JCP.2014.19.2.75.
The endoplasmic reticulum (ER) is the principal organelle responsible for multiple cellular functions including protein folding and maturation and the maintenance of cellular homeostasis. ER stress is activated by a variety of factors and triggers the unfolded protein response (UPR), which restores homeostasis or activates cell death. Multiple studies have clarified the link between ER stress and cancer, and particularly the involvement of the UPR. The UPR seems to adjust the paradoxical microenvironment of cancer and, as such, is one of resistance mechanisms against cancer therapy. This review describes the activity of different UPRs involved in tumorigenesis and resistance to cancer therapy.
内质网(ER)是负责多种细胞功能的主要细胞器,包括蛋白质折叠与成熟以及细胞内稳态的维持。内质网应激由多种因素激活,并触发未折叠蛋白反应(UPR),该反应可恢复内稳态或激活细胞死亡。多项研究阐明了内质网应激与癌症之间的联系,尤其是未折叠蛋白反应的参与情况。未折叠蛋白反应似乎在调节癌症矛盾的微环境,因此是抗癌治疗的抵抗机制之一。本综述描述了参与肿瘤发生和抗癌治疗抵抗的不同未折叠蛋白反应的活性。