Muthusami Sridhar, Ramachandran Ilangovan, Krishnamoorthy Sneha, Sambandam Yuvaraj, Ramalingam Satish, Queimado Lurdes, Chaudhuri Gautam, Ramachandran Ileng Kumaran
Department of Biochemistry, Karpagam Academy of Higher Education, Coimbatore 641 021, Tamil Nadu, India.
Department of Endocrinology, Dr. ALM PG Institute of Basic Medical Sciences, University of Madras, Taramani Campus, Chennai 600 113, Tamil Nadu, India.
Endocr Metab Immune Disord Drug Targets. 2021;21(1):67-76. doi: 10.2174/1871530320666200917112802.
The development of colorectal cancer (CRC) is a multistage process. The inflammation of the colon as in inflammatory bowel disease (IBD) such as ulcerative colitis (UC) or Crohn's disease (CD) is often regarded as the initial trigger for the development of inflammation-associated CRC. Many cytokines such as tumor necrosis factor alpha (TNF-α) and interleukins (ILs) are known to exert proinflammatory actions, and inflammation initiates or promotes tumorigenesis of various cancers, including CRC, through differential regulation of microRNAs (miRNAs/miRs). miRNAs can be oncogenic miRNAs (oncomiRs) or anti-oncomiRs/tumor suppressor miRNAs, and they play key roles during colorectal carcinogenesis. However, the functions and molecular mechanisms of regulation of miRNAs involved in inflammation-associated CRC are still anecdotal and largely unknown. Consolidating the published results and offering perspective solutions to circumvent CRC, the current review is focused on the role of miRNAs and their regulation in the development of CRC. We have also discussed the model systems adapted by researchers to delineate the role of miRNAs in inflammation-associated CRC.
结直肠癌(CRC)的发生是一个多阶段过程。结肠炎症,如炎症性肠病(IBD)中的溃疡性结肠炎(UC)或克罗恩病(CD),通常被视为炎症相关CRC发生的初始触发因素。许多细胞因子,如肿瘤坏死因子α(TNF-α)和白细胞介素(ILs),已知具有促炎作用,并且炎症通过对微小RNA(miRNAs/miRs)的差异调节来启动或促进包括CRC在内的各种癌症的肿瘤发生。miRNAs可以是致癌miRNAs(癌基因miRNAs)或抗致癌miRNAs/肿瘤抑制miRNAs,它们在结直肠癌发生过程中起关键作用。然而,参与炎症相关CRC的miRNAs的功能和调控分子机制仍然是零散的,并且在很大程度上尚不清楚。为了整合已发表的结果并提供规避CRC的前瞻性解决方案,本综述聚焦于miRNAs及其调控在CRC发生中的作用。我们还讨论了研究人员为描述miRNAs在炎症相关CRC中的作用而采用的模型系统。