Chemotherapy-induced miR-141 /MAP4K4 signaling suppresses progression of colorectal cancer

• Published in: Bioscience reports Vol. 38; no. 6
• Main Authors: Wang, Feifei, Zhao, Lianmei, Zhang, Juan, Meng, Zesong, Zhou, Chaoxi, Wang, Guanglin, Liu, Youqiang, Li, Meng, Xi, Jinchuan, Niu, Wenbo, Wang, Guiying
• Format: Journal Article
• Language: English
• Published: England Portland Press Ltd 21.12.2018
• Subjects: Animals; Apoptosis - drug effects; Cell Proliferation - drug effects; Cell Survival - drug effects; Colorectal Neoplasms - drug therapy; Colorectal Neoplasms - genetics; Colorectal Neoplasms - pathology; Disease Progression; Drug Resistance, Neoplasm - genetics; Fluorouracil - pharmacology; Gene Expression Regulation, Neoplastic - drug effects; HCT116 Cells; Humans; Intracellular Signaling Peptides and Proteins - genetics; Mice; MicroRNAs - genetics; Protein-Serine-Threonine Kinases - genetics; Signal Transduction - drug effects; Xenograft Model Antitumor Assays; miR-141; Colorectal cancer; 5-FU; MAP4K4
• ISSN: 0144-8463; 1573-4935
• DOI: 10.1042/BSR20180978

One of the treatment failures for colorectal cancer (CRC) is resistance to chemotherapy drugs. miRNAs have been demonstrated to be a new regulator of pathobiological processes in various tumors. While few studies have explored the specific role of in mediating 5-fluorouracil (5-FU) sensitivity of CRC cells, the present study aimed to detect the contribution of in 5-FU sensitivity. The CRC cells viability was measured by MTS assay and cell colony forming. The expression of and its downstream targets were assessed by reverse transcription quantitative PCR, Western blotting, and immunohistochemistry. The functional assays were conducted using CRC cells and nude mice. At the present study, we found overexpression of could inhibit proliferation, migration, tumor-forming and invasive potential of CRC cells and mitogen-activated protein kinase kinase kinase kinase 4 (MAP4K4) was verified as a directed target of The combination treatment of with 5-FU, directly targetting MAP4K4, could better inhibit invasion and metastasis of CRC cells colony than either one alone. Furthermore, overexpression of , targetting MAP4K4, enhanced the effected of 5-FU and suppressed the malignant biological behaviors, Our findings showed that 5-FU inhibited malignant behavior of human CRC cells and by enhancing the efficiency of Our data suggested that targetting the /MAP4K4 signaling pathway could be a potential molecular target that may enhance chemotherapeutic efficacy in the treatment of CRC.