Biological roles and molecular mechanism of circular RNAs in epithelial-mesenchymal transition of gastrointestinal malignancies

被引:0
作者
Fang, Ziyi [1 ,2 ]
Shao, Yongfu [1 ,2 ]
Hu, Meng [1 ]
Yan, Jianing [2 ]
Ye, Guoliang [2 ]
机构
[1] Ningbo Univ, Hlth Sci Ctr, Sch Basic Med Sci, Ningbo 315211, Peoples R China
[2] Ningbo Univ, Affiliated Hosp 1, Dept Gastroenterol, Ningbo 315020, Peoples R China
基金
中国国家自然科学基金;
关键词
Epithelial-mesenchymal transition; Circular RNAs (circRNAs); Gastrointestinal malignancies; GASTRIC-CANCER CELLS; REPRESSES E-CADHERIN; HEPATOCELLULAR-CARCINOMA; COLORECTAL-CANCER; TUMOR MICROENVIRONMENT; TRANSCRIPTION FACTOR; COLON-CANCER; EMT; METASTASIS; PROGRESSION;
D O I
10.32604/or.2024.051589
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Circular RNAs (circRNAs) are formed by splicing of precursor RNAs and covalently linked at the 5 ' and 3 ' ends. Dysregulated circRNAs are closely related to the epithelial-mesenchymal transition (EMT) of gastrointestinal malignancies. CircRNAs, including circRNA_0008717, circGOT1, circ-DOCK5, circVPS33B, circPVT1, circMET, circOXCT1, circ_67835, circRTN4, circ_0087502, circFNDC38, circ_PTEN1, circPGPEP1, and circ-E-Cad are involved in the EMT process of gastrointestinal malignancies through a variety of mechanisms, such as regulating EMT-inducing transcription factors, signaling pathways, and tumor microenvironments. Gastrointestinal (GI) malignancies are common malignant tumors worldwide, and the heterogeneity and easy metastasis of gastrointestinal malignancies limit the effectiveness of medical treatments. Therefore, investigating the molecular mechanisms involved in the pathogenesis of gastrointestinal malignancies is essential for clinical treatment. This article summarizes the biological roles and molecular mechanism of circRNAs in EMT of gastrointestinal malignancies, providing a theoretical basis for applying EMT-related circRNAs in targeted therapy.
引用
收藏
页码:549 / 566
页数:18
相关论文
共 164 条
[1]  
Ferlay J, Colombet M, Soerjomataram I, Parkin DM, Pineros M, Znaor A, Et al., Cancer statistics for the year 2020: an overview, Int J Cancer, (2021)
[2]  
Ashrafizadeh M, Dai J, Torabian P, Nabavi N, Aref AR, Aljabali AAA, Et al., Circular RNAs in EMT-driven metastasis regulation: modulation of cancer cell plasticity, tumorigenesis and therapy resistance, Cell Mol Life Sci, 81, 1, (2024)
[3]  
Xiao X, Miao X, Duan S, Liu S, Cao Q, Wu R, Et al., Single-cell enzymatic screening for epithelial mesenchymal transition with an ultrasensitive superwetting droplet-array microchip, Small Methods, 7, 7, (2023)
[4]  
Wong SHM, Fang CM, Chuah LH, Leong CO, Ngai SC., E-cadherin: its dysregulation in carcinogenesis and clinical implications, Crit Rev Oncol Hematol, 121, pp. 11-22, (2018)
[5]  
Zhang X, Liu G, Kang Y, Dong Z, Qian Q, Ma X., N-cadherin expression is associated with acquisition of EMT phenotype and with enhanced invasion in erlotinib-resistant lung cancer cell lines, PLoS One, 8, 3, (2013)
[6]  
Shao Y, Chen L, Lu R, Zhang X, Xiao B, Ye G, Et al., Decreased expression of hsa_circ_0001895 in human gastric cancer and its clinical significances, Tumour Biol, 39, 4, (2017)
[7]  
Tao X, Shao Y, Yan J, Yang L, Ye Q, Wang Q, Et al., Biological roles and potential clinical values of circular RNAs in gastrointestinal malignancies, Cancer Biol Med, 18, 2, pp. 437-457, (2021)
[8]  
Luo B, Tang CM, Chen JS., CircRNA and gastrointestinal cancer, J Cell Biochem, 120, 7, pp. 10956-10963, (2019)
[9]  
Du WW, Fang L, Yang W, Wu N, Awan FM, Yang Z, Et al., Induction of tumor apoptosis through a circular RNA enhancing Foxo3 activity, Cell Death Differ, 24, 2, pp. 357-370, (2017)
[10]  
Du WW, Yang W, Liu E, Yang Z, Dhaliwal P, Yang BB., Foxo3 circular RNA retards cell cycle progression via forming ternary complexes with p21 and CDK2, Nucleic Acids Res, 44, 6, pp. 2846-2858, (2016)