DISE/6mer seed toxicity-a powerful anti-cancer mechanism with implications for other diseases.
Ashley Haluck-KangasMonal PatelBidur PaudelAparajitha VaidyanathanAndrea E MurmannMarcus E PeterPublished in: Journal of experimental & clinical cancer research : CR (2021)
micro(mi)RNAs are short noncoding RNAs that through their seed sequence (pos. 2-7/8 of the guide strand) regulate cell function by targeting complementary sequences (seed matches) located mostly in the 3' untranslated region (3' UTR) of mRNAs. Any short RNA that enters the RNA induced silencing complex (RISC) can kill cells through miRNA-like RNA interference when its 6mer seed sequence (pos. 2-7 of the guide strand) has a G-rich nucleotide composition. G-rich seeds mediate 6mer Seed Toxicity by targeting C-rich seed matches in the 3' UTR of genes critical for cell survival. The resulting Death Induced by Survival gene Elimination (DISE) predominantly affects cancer cells but may contribute to cell death in other disease contexts. This review summarizes recent findings on the role of DISE/6mer Seed Tox in cancer; its therapeutic potential; its contribution to therapy resistance; its selectivity, and why normal cells are protected. In addition, we explore the connection between 6mer Seed Toxicity and aging in relation to cancer and certain neurodegenerative diseases.
Keyphrases
- cell death
- induced apoptosis
- cell cycle arrest
- oxidative stress
- papillary thyroid
- genome wide
- gene expression
- squamous cell carcinoma
- stem cells
- signaling pathway
- dna methylation
- cell proliferation
- mesenchymal stem cells
- endoplasmic reticulum stress
- copy number
- bone marrow
- high glucose
- nucleic acid
- genome wide identification
- smoking cessation
- lymph node metastasis
- genetic diversity