Zhang Yujing, Huang Shuai, Yang Gang, Zou Lianhong, Huang Xin, Liu Sulai
Key Laboratory of Molecular Epidemiology of Hunan Province, School of Medicine, Hunan Normal University, Changsha, 410081, China.
Key Laboratory of Protein Chemistry and Developmental Biology of Fish of Ministry of Education, Hunan Normal University, Changsha, 410081, China.
J Cancer. 2021 Sep 23;12(22):6787-6795. doi: 10.7150/jca.62352. eCollection 2021.
Digestive cancer is one of the leading causes of cancer mortality in the world. Despite a number of studies being conducted, the exact mechanism for treating digestive cancer has not yet been fully understood. To survive, digestive cancer cells are subjected to various internal and external adverse factors, such as hypoxia, nutritional deficiencies or drug toxicity, resulting in accumulation of misfolded and unfolded protein in endoplasmic reticulum (ER) lumen further leading to ER stress and the unfolded protein response (UPR). During the last years, studies on the relationship between ER stress and microRNAs (miRNAs) has burst on the scene. miRNAs are non-coding RNAs with a length of 21~22nucleotides involved in post-transcriptional regulation of gene expression, which could be regarded as oncomiRs (tumor inducers) and tumor suppressors regulating cancer cell proliferation, invasion, and apoptosis by differently affecting the expression of genes related to cancer cell signaling. Therefore, investigating the interaction between ER stress and miRNAs is crucial for developing effective cancer treatment and prevention strategies. In this review, we mainly discuss miRNAs focusing on its regulation, role in ER stress induced apoptosis in Digestive cancer, expound the underlying mechanism, thus provides a theoretical foundation for finding new therapeutic targets of digestive cancer.
消化道癌是全球癌症死亡的主要原因之一。尽管已经开展了多项研究,但消化道癌的确切治疗机制尚未完全明确。为了生存,消化道癌细胞会受到各种内部和外部不利因素的影响,如缺氧、营养缺乏或药物毒性,导致内质网(ER)腔中错误折叠和未折叠蛋白的积累,进而引发内质网应激和未折叠蛋白反应(UPR)。在过去几年中,内质网应激与微小RNA(miRNA)之间关系的研究迅速兴起。miRNA是长度为21至22个核苷酸的非编码RNA,参与基因表达的转录后调控,可被视为癌基因(肿瘤诱导物)和肿瘤抑制因子,通过不同程度地影响与癌细胞信号传导相关基因的表达来调节癌细胞的增殖、侵袭和凋亡。因此,研究内质网应激与miRNA之间的相互作用对于制定有效的癌症治疗和预防策略至关重要。在本综述中,我们主要讨论miRNA,重点关注其在消化道癌内质网应激诱导凋亡中的调控和作用,阐述其潜在机制,从而为寻找消化道癌新的治疗靶点提供理论基础。