LMCD1 antisense RNA 1 is a newly identified long noncoding RNA

Anticancer Drugs. 2022 Jan 1;33(1):1-5. doi: 10.1097/CAD.0000000000001124.

Abstract

Long noncoding RNAs (lncRNAs) are one of the interesting fields in cancer researches. LncRNAs are generally dysregulated in many diseases. LMCD1 antisense RNA 1 (LMCD1-AS1) is a newly identified lncRNA with protumorigenic functions on tumor cells. LMCD1-AS1 expression is increased in hepatocellular carcinoma (HCC). LMCD1-AS1 is a sponge of miR-106b-5p activity. LMCD1-AS1 modulates the survival of osteosarcoma via targeting miR-106b-5p. LMCD1-AS1 and Sp1 are highly expressed in osteosarcoma. SP1 can bind to the promoter region of LMCD1-AS1, resulting in its overexpression in osteosarcoma. GLI2 is shown to bind to the LMCD1-AS1 promoter and is transcriptionally activated by LMCD1-AS1. LMCD1 acts as a miR-1287-5p sponge to increase GLI2 expression. LMCD1 is abundantly expressed in kidney tissue. Moreover, it is functionally involved in protein-protein interactions with transcriptional co-repressor activity, including regulation of the calcineurin-NFAT signaling cascade known to play a critical role in recovery from acute kidney injury (AKI). The E2F1/LMCD1-AS1/miR-345-5p/COL6A3 axis is a newly identified regulatory mechanism, which has a function in cholangiocarcinoma (CCA) tumorigenesis and progression and provides potential therapeutic targets for CCA. Also, LMCD1-AS1 functions in thyroid cancer (THCA) development. LMCD1-AS1 is overexpressed in THCA cells, and LMCD1-AS1 knockdown suppresses the malignant phenotypes of THCA cells. In THCA development, LMCD1-AS1 exerts protumorigenic function through sponging miR-1287-5p to increase GLI2 expression, constituting a feedback loop of LMCD1-AS1/miR-1287-5p/GLI2. In this review, the author focuses on the molecular mechanisms of newly identified long noncoding RNA LMCD1 antisense RNA 1 (LMCD1-AS1).

MeSH terms

  • Acute Kidney Injury / pathology
  • Calcineurin / metabolism
  • Carcinogenesis / metabolism
  • Co-Repressor Proteins / metabolism*
  • Humans
  • Immunoglobulins / metabolism
  • LIM Domain Proteins / metabolism*
  • MicroRNAs / metabolism*
  • NFATC Transcription Factors / metabolism
  • Neoplasms / pathology*
  • Nuclear Proteins / metabolism
  • RNA, Antisense / metabolism*
  • RNA, Long Noncoding / metabolism*
  • Signal Transduction / physiology
  • Zinc Finger Protein Gli2 / metabolism

Substances

  • Co-Repressor Proteins
  • GLI2 protein, human
  • Immunoglobulins
  • LIM Domain Proteins
  • LMCD1 protein, human
  • MIRN1287 microRNA, human
  • MicroRNAs
  • NFATC Transcription Factors
  • Nuclear Proteins
  • RNA, Antisense
  • RNA, Long Noncoding
  • SP1 antigen
  • Zinc Finger Protein Gli2
  • Calcineurin