Identification and functional analysis of N6-methyladenine (m6 A)-related lncRNA across 33 cancer types

Cancer Med. 2023 Jan;12(2):2104-2116. doi: 10.1002/cam4.5001. Epub 2022 Jul 4.

Abstract

Background: N6-methyladenosine (m6 A) plays an essential role in tumorigenesis and cancer progression. Long noncoding RNAs (lncRNAs) are discovered to be important targets of m6 A modification, and they play fundamental roles in diverse biological processes. However, there is still a lack of knowledge with regards to the association between m6 A and lncRNAs in human tumors.

Methods: The relationship between lncRNAs and 21 m6 A regulators was comprehensively explored, through the integration of multi-omics data from M6A2Target, m6A-Atlas, and TCGA (The Cancer Genome Atlas). In order to explore the potential roles of m6A-related lncRNAs in human tumors, three applicable methods were introduced, which include the construction of ceRNA networks, drug sensitivity estimation, and survival analysis.

Results: A substantial number of positive correlation events across 33 cancer types were found. Moreover, cancer-specific lncRNAs were associated with tissue specificity, and cancer-common lncRNAs were conserved in cancer-related biological function. In particular, the m6 A-related lncRNA FGD5-AS1 was found to be associated with cancer treatment, through its influence on cisplatin resistance in breast cancer patients. Finally, a user-friendly interface Lnc2m6A, which is enriched with various browsing sections resource for the exhibition of relationships and putative biogenesis between lncRNAs and m6 A modifications, is offered in http://hainmu-biobigdata.com/Lnc2m6A.

Conclusions: In summary, the results from this paper will provide a valuable resource that guides both mechanistic and therapeutic roles of m6 A-related lncRNAs in human tumors.

Keywords: ceRNA; drug sensitivity; lncRNA; m6A; pan-cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine
  • Breast Neoplasms*
  • Carcinogenesis
  • Cell Transformation, Neoplastic
  • Female
  • Humans
  • RNA, Long Noncoding* / genetics

Substances

  • RNA, Long Noncoding
  • Adenosine