Clinical, Cosmetic and Investigational Dermatology (Apr 2022)

LncRNA LNCOC1 is Upregulated in Melanoma and Serves as a Potential Regulatory Target of miR-124 to Suppress Cancer Cell Invasion and Migration

  • Liu C,
  • Ding X,
  • Wei C,
  • Pei Y,
  • Meng F,
  • Zhong Y,
  • Liu Y

Journal volume & issue
Vol. Volume 15
pp. 751 – 762

Abstract

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Changhai Liu,1 Xiangsheng Ding,1 Cuie Wei,1 Yongdong Pei,1 Fanjun Meng,1 Yuren Zhong,1 Yi Liu2 1Department of Burn and Plastic Surgery, The First Affiliated of Hospital of Kangda College of Nanjing Medical University/The First People’s Hospital of Lianyungang, Lianyungang, People’s Republic of China; 2Department of Burn Plastic Surgery and Wound Repair, Second Hospital of Lanzhou University, Lanzhou, People’s Republic of ChinaCorrespondence: Changhai Liu, Department of Burn and Plastic Surgery, The First Affiliated of Hospital of Kangda College of Nanjing Medical University/The First People’s Hospital of Lianyungang, No. 6 Zhenhua East Road, Haizhou District, Lianyungang City, 222000, People’s Republic of China, Email [email protected] Yi Liu, Department of Burn Plastic Surgery and Wound Repair, Second Hospital of Lanzhou University, No. 82 Cuiyingmen, Chengguan District, Lanzhou City, 730030, People’s Republic of China, Email [email protected]: A cascade of genes and pathways have been reported in the precise regulation of malignant melanoma (MM). Previous study has demonstrated that lncRNA LNCOC1 is an oncogenic factor in the pathogenesis and development of various cancers. The present study explored the functionalities of LNCOC1 and its interactions with miR-124 in MM.Methods: A total of 65 melanoma patients were enrolled in this study. The expression of LNCOC1 and miR-124 after cell transfection were detected by RT-qPCR. The migration rates of SK-MEL-3 and A375 cells after transient transfection with LNCOC1 expression vector and miR-124 mimic was detected by trans-well assay.Results: LNCOC1 was accumulated to high levels in melanoma, and it was significantly correlated with the low survival rate of melanoma patients. Our bioinformatics data showed that miR-124 could target LNCOC1. Overexpression of miR-124 could downregulate LNCOC1. However, up-regulated the expression of LNCOC1 did not affect the expression of miR-124. Our correlation analysis also revealed that the expression of LNCOC1 and miR-124 were inversely correlated in both melanoma tissues and non-tumor tissues. The trans-well invasion and migration assays indicated that overexpression of miR-124 inhibited the melanoma cell invasion and migration. However, overexpression of LNCOC1 promoted melanoma cell invasion and migration.Conclusion: LNCOC1 is upregulated in melanoma, which can be considered as a potential target of miR-124 in modulating melanoma cell invasion and migration. LNCOC1 may also be an interfering target of MM therapy.Keywords: LNCOC1, miR-124, melanoma, invasion, migration

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