Cancer Management and Research (Nov 2020)

miR-141 Promotes Colon Cancer Cell Proliferation by Targeted PHLPP2 Expression Inhibitionn

  • Fang F,
  • Cheng L,
  • Wu X,
  • Ye M,
  • Zhang H

Journal volume & issue
Vol. Volume 12
pp. 11341 – 11350

Abstract

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Fazhuang Fang,1 Ling Cheng,2 Xiaotang Wu,2 Minfeng Ye,3 Huizhong Zhang1 1Department of Hepatobiliary, Pancreatic and Gastric Surgery, Jinhua Guangfu Hospital, Jinhua 321000, People’s Republic of China; 2Shanghai Engineering Research Center of Pharmaceutical Translation, Shanghai, People’s Republic of China; 3Department of Gastroenterology, Shaoxing People’s Hospital, Shaoxing, People’s Republic of ChinaCorrespondence: Huizhong ZhangDepartment of Hepatobiliary, Pancreatic and Gastric Surgery, Jinhua Guangfu Hospital, No. 1296 North Ring Road, Jinhua 321000, People’s Republic of ChinaTel +86 13735796710Email [email protected]: Colon cancer (CC) is the third most common cancer with a high rate of incidence and mortality. Therefore, it is highly necessary to explore novel targets of CC.Methods: The miRNA-seq and RNA-seq data of CC were accessed from the TCGA database. Differential analysis was performed using the “edgeR” package to identify differentially expressed miRNAs (DE_miRNAs). The downstream target genes of the target miRNA were then predicted by miRNA target prediction databases to identify the target mRNA. Normal colon cell line CCD-18Co and CC cell lines HCT-116, HT-29, SW620 and SW480 were chosen, and qRT-PCR was conducted to detect miR-141 expression in these cell lines. qRT-PCR and Western blot were carried out to determine PHLPP2 mRNA and protein expression, respectively. Dual-luciferase reporter gene assay was performed to verify the targeting relationship between miR-141 and PHLPP2 3ʹUTR. CCK-8 assay and colony formation assay were carried out to detect cell proliferation. Meanwhile, tumor xenograft model in nude mice was constructed to assess CC cell tumorigenic ability in vivo.Results: miR-141 was markedly up-regulated in CC tissue. CC cell proliferation and in vivo tumorigenic ability were suppressed by miR-141 silencing but promoted by miR-141 over-expression. PHLPP2 was significantly down-regulated in cancer tissue. Dual-luciferase reporter gene assay indicated that miR-141 could bind to PHLPP2 3ʹUTR. PHLPP2 expression was noticeably elevated upon miR-141 deficiency but significantly inhibited upon miR-141 over-expression. CCK-8 and colony formation assay suggested that miR-141 facilitated CC cell proliferation by silencing PHLPP2.Conclusion: miR-141 promotes CC cell proliferation by targeted silencing PHLPP2.Keywords: miR-141, PHLPP2, colon cancer, proliferation

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