Li Jiazhi, Zou Kun, Yu Lihui, Zhao Wenyue, Lu Ying, Mao Jun, Wang Bo, Wang Lu, Fan Shujun, Song Bo, Li Lianhong
Department of Pathology, Dalian Medical University, Dalian 116044, China.
Department of Oncology Radiology, The First Affiliated Hospital of Dalian Medical University, Dalian 116023, China.
Mol Ther Nucleic Acids. 2018 Mar 2;10:426-437. doi: 10.1016/j.omtn.2017.12.022. Epub 2018 Jan 4.
MicroRNA-140, a cartilage-specific microRNA, has recently been implicated in the cancer progression. However, the comprehensive role of miR-140 in the invasion and metastasis of colorectal cancer (CRC) is still not fully understood. In this study, we confirmed that miR-140 downregulates SMAD family member 3 (Smad3), which is a key downstream effector of the TGF-β signaling pathway, at the translational level in the CRC cell lines. Ectopic expression of miR-140 inhibits the process of epithelial-mesenchymal transition (EMT), at least partially through targeting Smad3, and induces the suppression of migratory and invasive capacities of CRC cells in vitro. miR-140 also attenuates CRC cell proliferation possibly via downregulating Samd3. Furthermore, overexpression of miR-140 inhibits the tumor formation and metastasis of CRC in vivo, and silenced Smad3 has the similar effect. Additionally, miR-140 expression is decreased in the clinical primary CRC specimens and appears as a progressive reduction in the metastatic specimens, whereas Smad3 is overexpressed in the CRC samples. Taken together, our findings suggest that miR-140 might be a key suppressor of CRC progression and metastasis through inhibiting EMT process by targeting Smad3. miR-140 may represent a novel candidate for CRC treatment.
微小RNA-140是一种软骨特异性微小RNA,最近被认为与癌症进展有关。然而,miR-140在结直肠癌(CRC)侵袭和转移中的全面作用仍未完全明确。在本研究中,我们证实miR-140在CRC细胞系的翻译水平下调SMAD家族成员3(Smad3),Smad3是TGF-β信号通路的关键下游效应因子。miR-140的异位表达至少部分通过靶向Smad3抑制上皮-间质转化(EMT)过程,并在体外诱导CRC细胞迁移和侵袭能力的抑制。miR-140还可能通过下调Samd3减弱CRC细胞增殖。此外,miR-140的过表达在体内抑制CRC的肿瘤形成和转移,沉默Smad3也有类似效果。另外,miR-140在临床原发性CRC标本中的表达降低,且在转移标本中呈逐渐降低趋势,而Smad3在CRC样本中过表达。综上所述,我们的研究结果表明,miR-140可能是通过靶向Smad3抑制EMT过程从而成为CRC进展和转移的关键抑制因子。miR-140可能代表一种用于CRC治疗的新型候选物。