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DISE/6mer seed toxicity-a powerful anti-cancer mechanism with implications for other diseases

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 comp...

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Autores principales: Haluck-Kangas, Ashley, Patel, Monal, Paudel, Bidur, Vaidyanathan, Aparajitha, Murmann, Andrea E., Peter, Marcus E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8662895/
https://www.ncbi.nlm.nih.gov/pubmed/34893072
http://dx.doi.org/10.1186/s13046-021-02177-1
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author Haluck-Kangas, Ashley
Patel, Monal
Paudel, Bidur
Vaidyanathan, Aparajitha
Murmann, Andrea E.
Peter, Marcus E.
author_facet Haluck-Kangas, Ashley
Patel, Monal
Paudel, Bidur
Vaidyanathan, Aparajitha
Murmann, Andrea E.
Peter, Marcus E.
author_sort Haluck-Kangas, Ashley
collection PubMed
description 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.
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spelling pubmed-86628952021-12-13 DISE/6mer seed toxicity-a powerful anti-cancer mechanism with implications for other diseases Haluck-Kangas, Ashley Patel, Monal Paudel, Bidur Vaidyanathan, Aparajitha Murmann, Andrea E. Peter, Marcus E. J Exp Clin Cancer Res Review 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. BioMed Central 2021-12-10 /pmc/articles/PMC8662895/ /pubmed/34893072 http://dx.doi.org/10.1186/s13046-021-02177-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Haluck-Kangas, Ashley
Patel, Monal
Paudel, Bidur
Vaidyanathan, Aparajitha
Murmann, Andrea E.
Peter, Marcus E.
DISE/6mer seed toxicity-a powerful anti-cancer mechanism with implications for other diseases
title DISE/6mer seed toxicity-a powerful anti-cancer mechanism with implications for other diseases
title_full DISE/6mer seed toxicity-a powerful anti-cancer mechanism with implications for other diseases
title_fullStr DISE/6mer seed toxicity-a powerful anti-cancer mechanism with implications for other diseases
title_full_unstemmed DISE/6mer seed toxicity-a powerful anti-cancer mechanism with implications for other diseases
title_short DISE/6mer seed toxicity-a powerful anti-cancer mechanism with implications for other diseases
title_sort dise/6mer seed toxicity-a powerful anti-cancer mechanism with implications for other diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8662895/
https://www.ncbi.nlm.nih.gov/pubmed/34893072
http://dx.doi.org/10.1186/s13046-021-02177-1
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