Regulating Protein-RNA Interactions: Advances in Targeting the LIN28/Let-7 Pathway

Int J Mol Sci. 2024 Mar 22;25(7):3585. doi: 10.3390/ijms25073585.

Abstract

Originally discovered in C. elegans, LIN28 is an evolutionarily conserved zinc finger RNA-binding protein (RBP) that post-transcriptionally regulates genes involved in developmental timing, stem cell programming, and oncogenesis. LIN28 acts via two distinct mechanisms. It blocks the biogenesis of the lethal-7 (let-7) microRNA (miRNA) family, and also directly binds messenger RNA (mRNA) targets, such as IGF-2 mRNA, and alters downstream splicing and translation events. This review focuses on the molecular mechanism of LIN28 repression of let-7 and current strategies to overcome this blockade for the purpose of cancer therapy. We highlight the value of the LIN28/let-7 pathway as a drug target, as multiple oncogenic proteins that the pathway regulates are considered undruggable due to their inaccessible cellular location and lack of cavities for small molecule binding.

Keywords: LIN28; gene therapy; let-7; miRNA; oncogene; small-molecule inhibitor.

Publication types

  • Review

MeSH terms

  • Animals
  • Caenorhabditis elegans / genetics
  • Carcinogenesis
  • Cell Transformation, Neoplastic
  • Humans
  • MicroRNAs* / genetics
  • RNA, Messenger

Substances

  • Lin28A protein, human
  • LIN28B protein, human
  • MicroRNAs
  • mirnlet7 microRNA, human
  • RNA, Messenger

Grants and funding

This work was supported by National Key R&D Program of China 2022YFA0912200, a startup fund from Wuhan University to L.W.