Cited by 29Cancer-related molecular mechanisms researchMicroRNA in disease regulationRNA modifications and cancer

LncRNA MALAT1 Promotes the Proliferation, Migration, and Invasion of Melanoma Cells by Downregulating miR-23a

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Wang, Pan, Hu, Liu, Fu, Guili, Lu, Jingjing, Zheng, Yuanquan, Li, Ying, Jia, Lin·2020·Cancer Management and Research

Abstract

PURPOSE: This study was designed to investigate the relationship between long-chain non-coding RNA metastasis-associated lung adenocarcinoma transcript 1 (lncRNA MALAT1)/miR-23a-23a and melanoma. PATIENTS AND METHODS: Fifty-two cases of corresponding non-tumor normal tissues and 109 cases (including 62 cases of primary melanoma and 47 cases of metastatic melanoma) were collected. Real-time fluorescent PCR quantified lncRNA MALAT1 and miR-23a, and counted the 3-year survival of high/low miR-23 and high/low lncRNA MALAT1 populations. We predicted the binding site according to the sequence information of lncRNA MALAT1 and miR-23a. lncRNA MALAT1 siRNA and miR-23a mimics vectors were constructed and transfected into melanoma cell lines respectively to observe their effects on cells. RESULTS: Compared with corresponding non-tumor normal tissues, lncRNA MALAT1 in melanoma tissue increased while miR-23a decreased. Compared with primary melanoma, metastatic melanoma was higher and miR-23a was lower. Downregulation of lncRNA MALAT1 caused upregulation of miR-23a, and lncRNA MALAT1 could bind to miR-23a. Downregulating lncRNA MALAT1 or upregulating miR-23a inhibited cell proliferation, migration and invasion and promoted apoptosis. Rescue experiments revealed that downregulation of miR-23a could offset cell changes caused by downregulation of lncRNA MALAT1. CONCLUSION: lncRNA MALAT1 promotes malignant proliferation of melanoma cells through miR-23a.

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  • Downregulation of Malat1 or MEG3 leads to an increase in miR-23a levels, consequently promoting tumor cell proliferation, migration, and invasion.

    “A downregulation of Malat1 or MEG3 leads to an increase in miR-23a levels, consequently promoting tumor cell proliferation, migration, and invasion [100,101].”

    From Recent advances of miR-23 in human diseases and growth development (2025) · cites this paper as [100]

    The Abstract (Results; page not specified) reports that MALAT1 downregulation raises miR-23a levels but inhibits, rather than promotes, melanoma-cell proliferation, migration, and invasion. The Results section on miR-23a confirms that increasing miR-23a inhibits these behaviors. The supplied passages do not address MEG3. (LLM, conf=0.93)

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  • In melanoma and pituitary tumors, miR-23a binds to lncRNA Malat1 and MEG3.

    “in melanoma and pituitary tumors, miR-23a binds to lncRNA Malat1 and MEG3.”

    From Recent advances of miR-23 in human diseases and growth development (2025) · cites this paper as [100]

    The Results section (“miR-23a is the Target Gene of lncRNA MALAT1”; page unavailable) reports sequence pairing and a luciferase assay supporting MALAT1–miR-23a binding in melanoma cells. The paper does not report this interaction with MEG3 in pituitary tumors; its References section mentions a MEG3–miR-23a study in laryngeal cancer instead. (LLM, conf=0.90)

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Authors
Wang, P., Hu, L., Fu, G., Lu, J., Zheng, Y., Li, Y., & Jia, L.
Affiliations
  • Wuhan Children's Hospital (CN)
  • Hubei Cancer Hospital (CN)
  • Central Hospital of Wuhan (CN)
Corresponding author
Li, Ying
Venue
Cancer Management and Research
Published
2020-07
Volume
Volume 12
Pages
6553-6562
ISSN
1179-1322 (ISSN-L)
OpenAlex
W3045628124
Cited by
29
References
30
Citations by year
2025: 4 · 2024: 7 · 2023: 1 · 2022: 7 · 2021: 9 · 2020: 1
FWCI
1.54
Type
journal article
Language
en
Open access
Locations
  • Cancer Management and Research (publishedVersion, cc-by-nc)
  • PubMed Central (publishedVersion, cc-by-nc)
  • PubMed (publishedVersion)
  • Dove Medical Press (Taylor and Francis Group) (submittedVersion, cc-by-nc)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer-related molecular mechanisms research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA modifications and cancer
Keywords
MALAT1, miR-23a, melanoma, metastatic melanoma, cell proliferation, cell migration, cell invasion, apoptosis, lncRNA-miRNA interaction, microRNA downregulation

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