Cargando…
Musashi–1—A Stemness RBP for Cancer Therapy?
SIMPLE SUMMARY: Musashi–1 (MSI1) is an RNA–binding protein that promotes stemness properties. It was initially discovered as a regulator of neuronal development and oocyte maturation in flies and frogs. Due to its specific expression pattern with high levels during development and in a variety of ca...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148009/ https://www.ncbi.nlm.nih.gov/pubmed/34062997 http://dx.doi.org/10.3390/biology10050407 |
_version_ | 1783697757439000576 |
---|---|
author | Bley, Nadine Hmedat, Ali Müller, Simon Rolnik, Robin Rausch, Alexander Lederer, Marcell Hüttelmaier, Stefan |
author_facet | Bley, Nadine Hmedat, Ali Müller, Simon Rolnik, Robin Rausch, Alexander Lederer, Marcell Hüttelmaier, Stefan |
author_sort | Bley, Nadine |
collection | PubMed |
description | SIMPLE SUMMARY: Musashi–1 (MSI1) is an RNA–binding protein that promotes stemness properties. It was initially discovered as a regulator of neuronal development and oocyte maturation in flies and frogs. Due to its specific expression pattern with high levels during development and in a variety of cancers, MSI1 evolved as an interesting target for cancer therapy. In cancer cells, the protein mainly promotes an undifferentiated state enhancing cancer growth and therapy resistance. In this review, we summarize previous findings from development of other organisms, outline MSI1′s expression and function in different cancer entities and highlight the development of MSI1–directed inhibitors. ABSTRACT: The RNA–binding protein Musashi–1 (MSI1) promotes stemness during development and cancer. By controlling target mRNA turnover and translation, MSI1 is implicated in the regulation of cancer hallmarks such as cell cycle or Notch signaling. Thereby, the protein enhanced cancer growth and therapy resistance to standard regimes. Due to its specific expression pattern and diverse functions, MSI1 represents an interesting target for cancer therapy in the future. In this review we summarize previous findings on MSI1′s implications in developmental processes of other organisms. We revisit MSI1′s expression in a set of solid cancers, describe mechanistic details and implications in MSI1 associated cancer hallmark pathways and highlight current research in drug development identifying the first MSI1–directed inhibitors with anti–tumor activity. |
format | Online Article Text |
id | pubmed-8148009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-81480092021-05-26 Musashi–1—A Stemness RBP for Cancer Therapy? Bley, Nadine Hmedat, Ali Müller, Simon Rolnik, Robin Rausch, Alexander Lederer, Marcell Hüttelmaier, Stefan Biology (Basel) Review SIMPLE SUMMARY: Musashi–1 (MSI1) is an RNA–binding protein that promotes stemness properties. It was initially discovered as a regulator of neuronal development and oocyte maturation in flies and frogs. Due to its specific expression pattern with high levels during development and in a variety of cancers, MSI1 evolved as an interesting target for cancer therapy. In cancer cells, the protein mainly promotes an undifferentiated state enhancing cancer growth and therapy resistance. In this review, we summarize previous findings from development of other organisms, outline MSI1′s expression and function in different cancer entities and highlight the development of MSI1–directed inhibitors. ABSTRACT: The RNA–binding protein Musashi–1 (MSI1) promotes stemness during development and cancer. By controlling target mRNA turnover and translation, MSI1 is implicated in the regulation of cancer hallmarks such as cell cycle or Notch signaling. Thereby, the protein enhanced cancer growth and therapy resistance to standard regimes. Due to its specific expression pattern and diverse functions, MSI1 represents an interesting target for cancer therapy in the future. In this review we summarize previous findings on MSI1′s implications in developmental processes of other organisms. We revisit MSI1′s expression in a set of solid cancers, describe mechanistic details and implications in MSI1 associated cancer hallmark pathways and highlight current research in drug development identifying the first MSI1–directed inhibitors with anti–tumor activity. MDPI 2021-05-05 /pmc/articles/PMC8148009/ /pubmed/34062997 http://dx.doi.org/10.3390/biology10050407 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Bley, Nadine Hmedat, Ali Müller, Simon Rolnik, Robin Rausch, Alexander Lederer, Marcell Hüttelmaier, Stefan Musashi–1—A Stemness RBP for Cancer Therapy? |
title | Musashi–1—A Stemness RBP for Cancer Therapy? |
title_full | Musashi–1—A Stemness RBP for Cancer Therapy? |
title_fullStr | Musashi–1—A Stemness RBP for Cancer Therapy? |
title_full_unstemmed | Musashi–1—A Stemness RBP for Cancer Therapy? |
title_short | Musashi–1—A Stemness RBP for Cancer Therapy? |
title_sort | musashi–1—a stemness rbp for cancer therapy? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148009/ https://www.ncbi.nlm.nih.gov/pubmed/34062997 http://dx.doi.org/10.3390/biology10050407 |
work_keys_str_mv | AT bleynadine musashi1astemnessrbpforcancertherapy AT hmedatali musashi1astemnessrbpforcancertherapy AT mullersimon musashi1astemnessrbpforcancertherapy AT rolnikrobin musashi1astemnessrbpforcancertherapy AT rauschalexander musashi1astemnessrbpforcancertherapy AT lederermarcell musashi1astemnessrbpforcancertherapy AT huttelmaierstefan musashi1astemnessrbpforcancertherapy |