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The role of HOPX in normal tissues and tumor progression
The homeodomain-only protein homeobox (HOPX) as the smallest homeodomain protein, lacks certain conserved residues required for DNA binding. Through our literature search, we reviewed the current understandings of HOPX in normal tissues and tumor progression. HOPX was initially identified as a criti...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997107/ https://www.ncbi.nlm.nih.gov/pubmed/31934721 http://dx.doi.org/10.1042/BSR20191953 |
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author | Liu, Yijun Zhang, Wenling |
author_facet | Liu, Yijun Zhang, Wenling |
author_sort | Liu, Yijun |
collection | PubMed |
description | The homeodomain-only protein homeobox (HOPX) as the smallest homeodomain protein, lacks certain conserved residues required for DNA binding. Through our literature search, we reviewed the current understandings of HOPX in normal tissues and tumor progression. HOPX was initially identified as a critical transcription factor in various normal tissues, which interacted with serum response factor (SRF) or other substance to regulate normal physiological function. However, HOPX is at a low expression or methylation level in tumors. These data indicated that HOPX may play a very important role in regulating differentiation phenotype and tumor suppressive function. We predicted the prognosis of HOPX in tumors from TCGA database and discussed the downstream genes of HOPX. To understand how HOPX is involved in the mechanisms between physical and pathological conditions could lead to novel therapeutic strategies for treatment. |
format | Online Article Text |
id | pubmed-6997107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69971072020-02-10 The role of HOPX in normal tissues and tumor progression Liu, Yijun Zhang, Wenling Biosci Rep Cancer The homeodomain-only protein homeobox (HOPX) as the smallest homeodomain protein, lacks certain conserved residues required for DNA binding. Through our literature search, we reviewed the current understandings of HOPX in normal tissues and tumor progression. HOPX was initially identified as a critical transcription factor in various normal tissues, which interacted with serum response factor (SRF) or other substance to regulate normal physiological function. However, HOPX is at a low expression or methylation level in tumors. These data indicated that HOPX may play a very important role in regulating differentiation phenotype and tumor suppressive function. We predicted the prognosis of HOPX in tumors from TCGA database and discussed the downstream genes of HOPX. To understand how HOPX is involved in the mechanisms between physical and pathological conditions could lead to novel therapeutic strategies for treatment. Portland Press Ltd. 2020-01-31 /pmc/articles/PMC6997107/ /pubmed/31934721 http://dx.doi.org/10.1042/BSR20191953 Text en © 2020 The Author(s). https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY). |
spellingShingle | Cancer Liu, Yijun Zhang, Wenling The role of HOPX in normal tissues and tumor progression |
title | The role of HOPX in normal tissues and tumor progression |
title_full | The role of HOPX in normal tissues and tumor progression |
title_fullStr | The role of HOPX in normal tissues and tumor progression |
title_full_unstemmed | The role of HOPX in normal tissues and tumor progression |
title_short | The role of HOPX in normal tissues and tumor progression |
title_sort | role of hopx in normal tissues and tumor progression |
topic | Cancer |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997107/ https://www.ncbi.nlm.nih.gov/pubmed/31934721 http://dx.doi.org/10.1042/BSR20191953 |
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