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Oncogenic and tumor suppressor function of MEIS and associated factors

MEIS proteins are historically associated with tumorigenesis, metastasis, and invasion in cancer. MEIS and associated PBX-HOX proteins may act as tumor suppressors or oncogenes in different cellular settings. Their expressions tend to be misregulated in various cancers. Bioinformatic analyses have s...

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Autores principales: GİRGİN, Birkan, KARADAĞ-ALPASLAN, Medine, KOCABAŞ, Fatih
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific and Technological Research Council of Turkey 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7759197/
https://www.ncbi.nlm.nih.gov/pubmed/33402862
http://dx.doi.org/10.3906/biy-2006-25
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author GİRGİN, Birkan
KARADAĞ-ALPASLAN, Medine
KOCABAŞ, Fatih
author_facet GİRGİN, Birkan
KARADAĞ-ALPASLAN, Medine
KOCABAŞ, Fatih
author_sort GİRGİN, Birkan
collection PubMed
description MEIS proteins are historically associated with tumorigenesis, metastasis, and invasion in cancer. MEIS and associated PBX-HOX proteins may act as tumor suppressors or oncogenes in different cellular settings. Their expressions tend to be misregulated in various cancers. Bioinformatic analyses have suggested their upregulation in leukemia/lymphoma, thymoma, pancreas, glioma, and glioblastoma, and downregulation in cervical, uterine, rectum, and colon cancers. However, every cancer type includes, at least, a subtype with high MEIS expression. In addition, studies have highlighted that MEIS proteins and associated factors may function as diagnostic or therapeutic biomarkers for various diseases. Herein, MEIS proteins and associated factors in tumorigenesis are discussed with recent discoveries in addition to how they could be modulated by noncoding RNAs or newly developed small-molecule MEIS inhibitors.
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spelling pubmed-77591972021-01-04 Oncogenic and tumor suppressor function of MEIS and associated factors GİRGİN, Birkan KARADAĞ-ALPASLAN, Medine KOCABAŞ, Fatih Turk J Biol Article MEIS proteins are historically associated with tumorigenesis, metastasis, and invasion in cancer. MEIS and associated PBX-HOX proteins may act as tumor suppressors or oncogenes in different cellular settings. Their expressions tend to be misregulated in various cancers. Bioinformatic analyses have suggested their upregulation in leukemia/lymphoma, thymoma, pancreas, glioma, and glioblastoma, and downregulation in cervical, uterine, rectum, and colon cancers. However, every cancer type includes, at least, a subtype with high MEIS expression. In addition, studies have highlighted that MEIS proteins and associated factors may function as diagnostic or therapeutic biomarkers for various diseases. Herein, MEIS proteins and associated factors in tumorigenesis are discussed with recent discoveries in addition to how they could be modulated by noncoding RNAs or newly developed small-molecule MEIS inhibitors. The Scientific and Technological Research Council of Turkey 2020-12-14 /pmc/articles/PMC7759197/ /pubmed/33402862 http://dx.doi.org/10.3906/biy-2006-25 Text en Copyright © 2020 The Author(s) This article is distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/ ), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Article
GİRGİN, Birkan
KARADAĞ-ALPASLAN, Medine
KOCABAŞ, Fatih
Oncogenic and tumor suppressor function of MEIS and associated factors
title Oncogenic and tumor suppressor function of MEIS and associated factors
title_full Oncogenic and tumor suppressor function of MEIS and associated factors
title_fullStr Oncogenic and tumor suppressor function of MEIS and associated factors
title_full_unstemmed Oncogenic and tumor suppressor function of MEIS and associated factors
title_short Oncogenic and tumor suppressor function of MEIS and associated factors
title_sort oncogenic and tumor suppressor function of meis and associated factors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7759197/
https://www.ncbi.nlm.nih.gov/pubmed/33402862
http://dx.doi.org/10.3906/biy-2006-25
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