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The Hippo signaling pathway in leukemia: function, interaction, and carcinogenesis
Cancer can be considered as a communication disease between and within cells; nevertheless, there is no effective therapy for the condition, and this disease is typically identified at its late stage. Chemotherapy, radiation, and molecular-targeted treatment are typically ineffective against cancer...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8710012/ https://www.ncbi.nlm.nih.gov/pubmed/34953494 http://dx.doi.org/10.1186/s12935-021-02408-7 |
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author | Noorbakhsh, Negar Hayatmoghadam, Bentolhoda Jamali, Marzieh Golmohammadi, Maryam Kavianpour, Maria |
author_facet | Noorbakhsh, Negar Hayatmoghadam, Bentolhoda Jamali, Marzieh Golmohammadi, Maryam Kavianpour, Maria |
author_sort | Noorbakhsh, Negar |
collection | PubMed |
description | Cancer can be considered as a communication disease between and within cells; nevertheless, there is no effective therapy for the condition, and this disease is typically identified at its late stage. Chemotherapy, radiation, and molecular-targeted treatment are typically ineffective against cancer cells. A better grasp of the processes of carcinogenesis, aggressiveness, metastasis, treatment resistance, detection of the illness at an earlier stage, and obtaining a better therapeutic response will be made possible. Researchers have discovered that cancerous mutations mainly affect signaling pathways. The Hippo pathway, as one of the main signaling pathways of a cell, has a unique ability to cause cancer. In order to treat cancer, a complete understanding of the Hippo signaling system will be required. On the other hand, interaction with other pathways like Wnt, TGF-β, AMPK, Notch, JNK, mTOR, and Ras/MAP kinase pathways can contribute to carcinogenesis. Phosphorylation of oncogene YAP and TAZ could lead to leukemogenesis, which this process could be regulated via other signaling pathways. This review article aimed to shed light on how the Hippo pathway interacts with other cellular signaling networks and its functions in leukemia. |
format | Online Article Text |
id | pubmed-8710012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87100122022-01-05 The Hippo signaling pathway in leukemia: function, interaction, and carcinogenesis Noorbakhsh, Negar Hayatmoghadam, Bentolhoda Jamali, Marzieh Golmohammadi, Maryam Kavianpour, Maria Cancer Cell Int Review Cancer can be considered as a communication disease between and within cells; nevertheless, there is no effective therapy for the condition, and this disease is typically identified at its late stage. Chemotherapy, radiation, and molecular-targeted treatment are typically ineffective against cancer cells. A better grasp of the processes of carcinogenesis, aggressiveness, metastasis, treatment resistance, detection of the illness at an earlier stage, and obtaining a better therapeutic response will be made possible. Researchers have discovered that cancerous mutations mainly affect signaling pathways. The Hippo pathway, as one of the main signaling pathways of a cell, has a unique ability to cause cancer. In order to treat cancer, a complete understanding of the Hippo signaling system will be required. On the other hand, interaction with other pathways like Wnt, TGF-β, AMPK, Notch, JNK, mTOR, and Ras/MAP kinase pathways can contribute to carcinogenesis. Phosphorylation of oncogene YAP and TAZ could lead to leukemogenesis, which this process could be regulated via other signaling pathways. This review article aimed to shed light on how the Hippo pathway interacts with other cellular signaling networks and its functions in leukemia. BioMed Central 2021-12-25 /pmc/articles/PMC8710012/ /pubmed/34953494 http://dx.doi.org/10.1186/s12935-021-02408-7 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 Noorbakhsh, Negar Hayatmoghadam, Bentolhoda Jamali, Marzieh Golmohammadi, Maryam Kavianpour, Maria The Hippo signaling pathway in leukemia: function, interaction, and carcinogenesis |
title | The Hippo signaling pathway in leukemia: function, interaction, and carcinogenesis |
title_full | The Hippo signaling pathway in leukemia: function, interaction, and carcinogenesis |
title_fullStr | The Hippo signaling pathway in leukemia: function, interaction, and carcinogenesis |
title_full_unstemmed | The Hippo signaling pathway in leukemia: function, interaction, and carcinogenesis |
title_short | The Hippo signaling pathway in leukemia: function, interaction, and carcinogenesis |
title_sort | hippo signaling pathway in leukemia: function, interaction, and carcinogenesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8710012/ https://www.ncbi.nlm.nih.gov/pubmed/34953494 http://dx.doi.org/10.1186/s12935-021-02408-7 |
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