4.4 Review

Cancer-associated miRNAs and their therapeutic potential

Journal

JOURNAL OF HUMAN GENETICS
Volume 66, Issue 9, Pages 937-945

Publisher

SPRINGERNATURE
DOI: 10.1038/s10038-021-00938-6

Keywords

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Funding

  1. JSPS [18K06954, 16K14630, 15H05908]
  2. MEXT, a research program of the Project for Cancer Research and Therapeutic Evolution (P-CREATE)
  3. Japan Agency for Medical Research and Development (AMED)
  4. Nanken-Kyoten, TMDU
  5. Grants-in-Aid for Scientific Research [16K14630, 15H05908, 18K06954] Funding Source: KAKEN

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miRNA plays a role in cancer development and its therapeutics hold promise in inhibiting oncogenic miRNA and replacing tumor suppressive miRNA, potentially improving cancer treatment outcomes.
MicroRNA (miRNA; miR) is a functionally small non-coding RNA and can negatively regulate gene expression by directly binding to the target gene. Some miRNAs are closely involved in the development and progression of cancer and are abnormally expressed in many cancer types. Therefore, control of the expression of cancer-associated miRNAs is expected as a next-generation drug modality to treat advanced types of cancers with high unmet medical needs. Indeed, miRNA therapeutics, which are based on the functional inhibition of oncogenic miRNA (OncomiR) using antisense oligonucleotides (anti-miR) and the replacement via the introduction of a synthetic miRNA mimic for tumor suppressive miRNA (TS-miR), have been developed. In this review, we summarize cancer-associated miRNAs related to various cancer pathologies and their clinical application to miRNA therapeutics for cancer.

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