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To Detach, Migrate, Adhere, and Metastasize: CD97/ADGRE5 in Cancer
Tumorigenesis is a multistep process, during which cells acquire a series of mutations that lead to unrestrained cell growth and proliferation, inhibition of cell differentiation, and evasion of cell death. Growing tumors stimulate angiogenesis, providing them with nutrients and oxygen. Ultimately,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9101421/ https://www.ncbi.nlm.nih.gov/pubmed/35563846 http://dx.doi.org/10.3390/cells11091538 |
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author | Aust, Gabriela Zheng, Leyu Quaas, Marianne |
author_facet | Aust, Gabriela Zheng, Leyu Quaas, Marianne |
author_sort | Aust, Gabriela |
collection | PubMed |
description | Tumorigenesis is a multistep process, during which cells acquire a series of mutations that lead to unrestrained cell growth and proliferation, inhibition of cell differentiation, and evasion of cell death. Growing tumors stimulate angiogenesis, providing them with nutrients and oxygen. Ultimately, tumor cells invade the surrounding tissue and metastasize; a process responsible for about 90% of cancer-related deaths. Adhesion G protein-coupled receptors (aGPCRs) modulate the cellular processes closely related to tumor cell biology, such as adhesion and detachment, migration, polarity, and guidance. Soon after first being described, individual human aGPCRs were found to be involved in tumorigenesis. Twenty-five years ago, CD97/ADGRE5 was discovered to be induced in one of the most severe tumors, dedifferentiated anaplastic thyroid carcinoma. After decades of research, the time has come to review our knowledge of the presence and function of CD97 in cancer. In summary, CD97 is obviously induced or altered in many tumor entities; this has been shown consistently in nearly one hundred published studies. However, its high expression at circulating and tumor-infiltrating immune cells renders the systemic targeting of CD97 in tumors difficult. |
format | Online Article Text |
id | pubmed-9101421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91014212022-05-14 To Detach, Migrate, Adhere, and Metastasize: CD97/ADGRE5 in Cancer Aust, Gabriela Zheng, Leyu Quaas, Marianne Cells Review Tumorigenesis is a multistep process, during which cells acquire a series of mutations that lead to unrestrained cell growth and proliferation, inhibition of cell differentiation, and evasion of cell death. Growing tumors stimulate angiogenesis, providing them with nutrients and oxygen. Ultimately, tumor cells invade the surrounding tissue and metastasize; a process responsible for about 90% of cancer-related deaths. Adhesion G protein-coupled receptors (aGPCRs) modulate the cellular processes closely related to tumor cell biology, such as adhesion and detachment, migration, polarity, and guidance. Soon after first being described, individual human aGPCRs were found to be involved in tumorigenesis. Twenty-five years ago, CD97/ADGRE5 was discovered to be induced in one of the most severe tumors, dedifferentiated anaplastic thyroid carcinoma. After decades of research, the time has come to review our knowledge of the presence and function of CD97 in cancer. In summary, CD97 is obviously induced or altered in many tumor entities; this has been shown consistently in nearly one hundred published studies. However, its high expression at circulating and tumor-infiltrating immune cells renders the systemic targeting of CD97 in tumors difficult. MDPI 2022-05-04 /pmc/articles/PMC9101421/ /pubmed/35563846 http://dx.doi.org/10.3390/cells11091538 Text en © 2022 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 Aust, Gabriela Zheng, Leyu Quaas, Marianne To Detach, Migrate, Adhere, and Metastasize: CD97/ADGRE5 in Cancer |
title | To Detach, Migrate, Adhere, and Metastasize: CD97/ADGRE5 in Cancer |
title_full | To Detach, Migrate, Adhere, and Metastasize: CD97/ADGRE5 in Cancer |
title_fullStr | To Detach, Migrate, Adhere, and Metastasize: CD97/ADGRE5 in Cancer |
title_full_unstemmed | To Detach, Migrate, Adhere, and Metastasize: CD97/ADGRE5 in Cancer |
title_short | To Detach, Migrate, Adhere, and Metastasize: CD97/ADGRE5 in Cancer |
title_sort | to detach, migrate, adhere, and metastasize: cd97/adgre5 in cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9101421/ https://www.ncbi.nlm.nih.gov/pubmed/35563846 http://dx.doi.org/10.3390/cells11091538 |
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