The role of miR-4469 as a tumor suppressor regulating inflammatory cell infiltration in colorectal cancer

被引:2
|
作者
Qi, Lu [1 ,2 ,3 ]
Wang, Lu [4 ,5 ]
Song, Fuyao [1 ,2 ,3 ]
Ding, Zhenhua [4 ,5 ]
Zhang, Ying [4 ,5 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Pathol, Guangzhou 510515, Peoples R China
[2] Southern Med Univ, Sch Basic Med Sci, Dept Pathol, Guangzhou 510515, Peoples R China
[3] Guangdong Prov Key Lab Mol Oncol Pathol, Guangzhou 510515, Peoples R China
[4] Southern Med Univ, Sch Publ Hlth, Dept Radiat Med, Guangzhou 510515, Peoples R China
[5] Guangdong Prov Key Lab Trop Dis Res, Guangzhou 510515, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
miR-4469; Colorectal cancer; Neutrophil; Tumor suppressor; GENE-EXPRESSION; PROMOTES; MICRORNAS; PROLIFERATION; BIOGENESIS; CYTOSCAPE; PROGNOSIS; SOFTWARE; MIR-34A;
D O I
10.1016/j.csbj.2022.07.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: MicroRNA (miRNA) regulates gene expression posttranscriptionally, and some of them function in tumor suppression and can be used in drug development. As a result, identifying and screening miRNAs that suppress tumors would be a significant addition to tumor treatment. Methods: In this study, we analyzed the miRNA expression profile of colorectal cancer (CRC), constructed a negative regulatory network of the miRNA-target genes, and identified miR-4469 as one of the key tumor suppressors miRNAs. We analyzed the expression and survival of miR-4469 in pan-cancer, experimentally verified the expression level of miR-4469 in CRC cells and the effect on CRC cell proliferation and migration. We screened miR-4469 target genes for enrichment analysis and immune cell infiltration analysis and validated target gene expression to clarify the regulatory mechanisms involved in miR-4469. Results: miR-4469 was more highly expressed in normal colorectum tissues compared to CRC tissues and correlated with survival time in patients with multiple cancers. It was shown that miR-4469 was highly expressed in normal colon cells and miR-4469 expression could inhibit the proliferation and migration of CRC cells. In addition, studies on the mechanism showed that miR-4469 function is mainly related to the regulation of inflammatory cell infiltration, and the key target genes of miR-4469 in this process are SLC2A3, FGR, PLEKHO2, and MYO1F. Conclusion: miR-4469 is a tumor suppressor in CRC, and its regulatory mechanism mainly affects the infiltration of inflammatory cells in the cancer tissue. (C) 2022 The Author(s). Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology.
引用
收藏
页码:3755 / 3763
页数:9
相关论文
共 50 条
  • [1] Tumor suppressor miR-137 inhibits colorectal cancer progression by negatively regulating cancer stem cell marker, Musashi-1
    Smith, Amber R.
    Marquez, Rebecca
    Tsao, Bryan
    Lan, Lan
    Pathak, Surajit
    Sun, Xiao-Feng
    Neufeld, Kristi
    Xu, Liang
    CANCER RESEARCH, 2014, 74 (19)
  • [2] CDK3, target of miR-4469, suppresses breast cancer metastasis via inhibiting Wnt/β-catenin pathway
    Cao, Ting
    Xiao, Tian
    Huang, Guanqun
    Xu, Yafei
    Zhu, Joe Jiang
    Wang, Kaixin
    Ye, Wencai
    Guan, Hong
    He, Jinsong
    Zheng, Duo
    ONCOTARGET, 2017, 8 (49) : 84917 - 84927
  • [3] Tumor Suppressor Functions of miR-133a in Colorectal Cancer
    Dong, Yujuan
    Zhao, Junhong
    Wu, Chung-Wah
    Zhang, Lijing
    Liu, Xiaodong
    Kang, Wei
    Leung, Wing-Wah
    Zhang, Ning
    Chan, Francis K. L.
    Sung, Joseph J. Y.
    Ng, Simon S. M.
    Yu, Jun
    MOLECULAR CANCER RESEARCH, 2013, 11 (09) : 1051 - 1060
  • [4] Detailed analysis of inflammatory cell infiltration in colorectal cancer
    Vayrynen, J. P.
    Tuomisto, A.
    Klintrup, K.
    Makela, J.
    Karttunen, T. J.
    Makinen, M. J.
    BRITISH JOURNAL OF CANCER, 2013, 109 (07) : 1839 - 1847
  • [5] Detailed analysis of inflammatory cell infiltration in colorectal cancer
    J P Väyrynen
    A Tuomisto
    K Klintrup
    J Mäkelä
    T J Karttunen
    M J Mäkinen
    British Journal of Cancer, 2013, 109 : 1839 - 1847
  • [6] The Role of Autophagy in Tumor Immune Infiltration in Colorectal Cancer
    Bian-fang, Yu
    Dong-ning, Wu
    Dan, Teng
    Jian-yu, Shi
    Shi-yi, Wang
    Ben-jun, Wang
    Xin, Dong
    Wen-wen, Zhao
    Qing-feng, Wang
    Yan, Zhao
    ANALYTICAL CELLULAR PATHOLOGY, 2022, 2022
  • [7] MiR-215 is a tumor suppressor in colorectal cancer in vitro and in vivo
    Vychytilova-Faltejskova, Petra
    Merhautova, Jana
    MIcochova, Jitka
    Radova, Lenka
    Iliev, Robert
    Svoboda, Marek
    Vyzula, Rostislav
    Slaby, Ondrej
    CANCER RESEARCH, 2015, 75
  • [8] Tumor Suppressor PTPRJ Is a Target of miR-155 in Colorectal Cancer
    Zhang, Xiao-Fei
    Tu, Rongfu
    Li, Keke
    Ye, Pengxiang
    Cui, Xiaofeng
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2017, 118 (10) : 3391 - 3400
  • [9] MiR-382 functions as tumor suppressor and chemosensitizer in colorectal cancer
    Yao, Hui
    Xia, Dong
    Li, Zong-lin
    Ren, Lei
    Wang, Ming-ming
    Chen, Wang-sheng
    Hu, Zheng-chuan
    Yi, Guo-ping
    Xu, Liang
    BIOSCIENCE REPORTS, 2019, 39
  • [10] MiR-4500 is epigenetically downregulated in colorectal cancer and functions as a novel tumor suppressor by regulating HMGA2
    Yu, Feng Yan
    Tu, Yun
    Deng, Ying
    Guo, Cancan
    Ning, Jue
    Zhu, Yuzhen
    Lv, Xiaohua
    Ye, Hua
    CANCER BIOLOGY & THERAPY, 2016, 17 (11) : 1149 - 1157