Tokarz Paulina, Blasiak Janusz
Department of Molecular Genetics, Faculty of Biology and Environmental Protection, University of Lodz, Łódź, Poland.
Acta Biochim Pol. 2012;59(4):467-74. Epub 2012 Nov 21.
microRNAs (miRNAs) are small, non-coding RNA molecules that regulate gene expression by targeting specific mRNAs. microRNAs play a role in several physiological processes in the cell, including migration, proliferation, differentiation and apoptosis. Apart from their role in regular metabolism, abnormal profiles of miRNA expression accompany cancer transformation, including colorectal cancer (CRC) metastasis. microRNAs may play a role in each phase of CRC metastasis including angiogenesis, invasion, intravasation, circulation, extravasation and metastatic colonization. microRNA levels may serve as a predictive CRC marker, which was confirmed by the serum level of miR-29a targeting KLF4, a marker of cell stemness, and the plasma level of miR-221 down-regulating c-Kit, Stat5A and ETS1, which are signal transducers and transcription factor, respectively. In turn, the level of miR-143 in CRC cells decreasing the amount of MACC1 (metastasis-associated in colon cancer-1) and oncogenic KRAS protein, may be utilized as a prognostic marker. Also, single nucleotide polymorphisms of genes encoding miRNAs, including miR-423 and miR-608, which correlate with tumor recurrence, may be useful as diagnostic, prognostic and predictive indicators in CRC metastasis. Pre-miR-34a and pre-miR-199a decreased the level of Axl, a tyrosine-protein kinase receptor, so they can be considered as drugs in antimetastatic therapy. On the other hand, miR-222 targeting ADAM-17, a disintegrin and metalloproteinase, and miR-328 interacting with ABCG2, an ABC transporter, may overcome drug resistance of cancer cells. microRNAs may be considered in wide-range application to facilitate CRC metastasis diagnosis, prognosis, prediction and therapy, however, further clinical, epidemiological and in vitro studies should be conducted to verify their utility.
微小RNA(miRNA)是一类小的非编码RNA分子,通过靶向特定的信使核糖核酸(mRNA)来调节基因表达。微小RNA在细胞的多个生理过程中发挥作用,包括迁移、增殖、分化和凋亡。除了在正常代谢中的作用外,miRNA表达异常与癌症转化相关,包括结直肠癌(CRC)转移。微小RNA可能在CRC转移的各个阶段发挥作用,包括血管生成、侵袭、内渗、循环、外渗和转移定植。微小RNA水平可作为CRC的预测标志物,这一点已通过靶向细胞干性标志物KLF4的miR-29a血清水平以及下调c-Kit、Stat5A和ETS1(分别为信号转导子和转录因子)的miR-221血浆水平得到证实。反过来,CRC细胞中miR-143水平降低了转移相关结肠癌-1(MACC1)和致癌性KRAS蛋白的量,可作为预后标志物。此外,编码miRNA的基因的单核苷酸多态性,包括与肿瘤复发相关的miR-423和miR-608,可能作为CRC转移的诊断、预后和预测指标。前体miR-34a和前体miR-199a降低了酪氨酸蛋白激酶受体Axl的水平,因此它们可被视为抗转移治疗的药物。另一方面,靶向解聚素和金属蛋白酶ADAM-17的miR-222以及与ABC转运蛋白ABCG2相互作用的miR-328可能克服癌细胞的耐药性。微小RNA可被广泛应用于促进CRC转移的诊断、预后、预测和治疗,然而,还应进行进一步的临床、流行病学和体外研究以验证其效用。