RNA-binding proteins regulating the CD44 alternative splicing

Alternative splicing is often deregulated in cancer, and cancer-specific isoform switches are part of the oncogenic transformation of cells. Accumulating evidence indicates that isoforms of the multifunctional cell-surface glycoprotein CD44 play different roles in cancer cells as compared to normal...

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Main Authors: Diana Maltseva, Alexander Tonevitsky
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-12-01
Series:Frontiers in Molecular Biosciences
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmolb.2023.1326148/full
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author Diana Maltseva
Alexander Tonevitsky
Alexander Tonevitsky
author_facet Diana Maltseva
Alexander Tonevitsky
Alexander Tonevitsky
author_sort Diana Maltseva
collection DOAJ
description Alternative splicing is often deregulated in cancer, and cancer-specific isoform switches are part of the oncogenic transformation of cells. Accumulating evidence indicates that isoforms of the multifunctional cell-surface glycoprotein CD44 play different roles in cancer cells as compared to normal cells. In particular, the shift of CD44 isoforms is required for epithelial to mesenchymal transition (EMT) and is crucial for the maintenance of pluripotency in normal human cells and the acquisition of cancer stem cells phenotype for malignant cells. The growing and seemingly promising use of splicing inhibitors for treating cancer and other pathologies gives hope for the prospect of using such an approach to regulate CD44 alternative splicing. This review integrates current knowledge about regulating CD44 alternative splicing by RNA-binding proteins.
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spelling doaj.art-85a52239a53d492ab82b26a15d7104fb2023-12-01T12:28:33ZengFrontiers Media S.A.Frontiers in Molecular Biosciences2296-889X2023-12-011010.3389/fmolb.2023.13261481326148RNA-binding proteins regulating the CD44 alternative splicingDiana Maltseva0Alexander Tonevitsky1Alexander Tonevitsky2Faculty of Biology and Biotechnology, HSE University, Moscow, RussiaFaculty of Biology and Biotechnology, HSE University, Moscow, RussiaShemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, RussiaAlternative splicing is often deregulated in cancer, and cancer-specific isoform switches are part of the oncogenic transformation of cells. Accumulating evidence indicates that isoforms of the multifunctional cell-surface glycoprotein CD44 play different roles in cancer cells as compared to normal cells. In particular, the shift of CD44 isoforms is required for epithelial to mesenchymal transition (EMT) and is crucial for the maintenance of pluripotency in normal human cells and the acquisition of cancer stem cells phenotype for malignant cells. The growing and seemingly promising use of splicing inhibitors for treating cancer and other pathologies gives hope for the prospect of using such an approach to regulate CD44 alternative splicing. This review integrates current knowledge about regulating CD44 alternative splicing by RNA-binding proteins.https://www.frontiersin.org/articles/10.3389/fmolb.2023.1326148/fullCD44 alternative splicing regulationCD44 isoformRNA-binding proteincancerESRP1
spellingShingle Diana Maltseva
Alexander Tonevitsky
Alexander Tonevitsky
RNA-binding proteins regulating the CD44 alternative splicing
Frontiers in Molecular Biosciences
CD44 alternative splicing regulation
CD44 isoform
RNA-binding protein
cancer
ESRP1
title RNA-binding proteins regulating the CD44 alternative splicing
title_full RNA-binding proteins regulating the CD44 alternative splicing
title_fullStr RNA-binding proteins regulating the CD44 alternative splicing
title_full_unstemmed RNA-binding proteins regulating the CD44 alternative splicing
title_short RNA-binding proteins regulating the CD44 alternative splicing
title_sort rna binding proteins regulating the cd44 alternative splicing
topic CD44 alternative splicing regulation
CD44 isoform
RNA-binding protein
cancer
ESRP1
url https://www.frontiersin.org/articles/10.3389/fmolb.2023.1326148/full
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