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Adipocytokines and disease progression in endometrial cancer: a systematic review
The objective of the study was to document the effect of adipocytokines on endometrial cancer progression. A search of the databases CINAHL, Medline, PubMed, Cochrane, Web of Science, Embase and Google Scholar was performed for English language articles from January 2000 to December 2020 using the k...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924097/ https://www.ncbi.nlm.nih.gov/pubmed/34951691 http://dx.doi.org/10.1007/s10555-021-10002-6 |
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author | Ray, Irene Meira, Lisiane B. Michael, Agnieszka Ellis, Patricia E. |
author_facet | Ray, Irene Meira, Lisiane B. Michael, Agnieszka Ellis, Patricia E. |
author_sort | Ray, Irene |
collection | PubMed |
description | The objective of the study was to document the effect of adipocytokines on endometrial cancer progression. A search of the databases CINAHL, Medline, PubMed, Cochrane, Web of Science, Embase and Google Scholar was performed for English language articles from January 2000 to December 2020 using the keywords: (Endometrial cancer) AND (progression OR metastasis) AND (adipocytokine OR adiponectin OR leptin OR visfatin OR IL-6 OR TNF-α OR adipokine OR cytokine). Forty-nine studies on adipocytokines have been included in this review. Adiponectin has been linked with anti-proliferative and anti-metastatic effects on endometrial cancer cells and is associated with a better prognosis. Leptin, visfatin and resistin are linked to the stimulation of endometrial cancer growth, proliferation, invasion and metastasis and are associated with worse prognosis or with a higher grade/stage of endometrial cancer. IL-6, Il-11, IL-31, IL-33, TNF-α, TGF-β1, SDF-1 and CXCR are involved in endometrial cancer cell growth and metastasis or involved in epithelial mesenchymal transformation (EMT) or associated with advanced disease. Adipocytokines have been found to directly impact endometrial cancer cell proliferation, invasion and migration. These molecules and their signalling pathways may be used to determine prognosis and course of the disease and may also be exploited as potential targets for cancer treatment and prevention of progression. |
format | Online Article Text |
id | pubmed-8924097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-89240972022-03-17 Adipocytokines and disease progression in endometrial cancer: a systematic review Ray, Irene Meira, Lisiane B. Michael, Agnieszka Ellis, Patricia E. Cancer Metastasis Rev Clinical The objective of the study was to document the effect of adipocytokines on endometrial cancer progression. A search of the databases CINAHL, Medline, PubMed, Cochrane, Web of Science, Embase and Google Scholar was performed for English language articles from January 2000 to December 2020 using the keywords: (Endometrial cancer) AND (progression OR metastasis) AND (adipocytokine OR adiponectin OR leptin OR visfatin OR IL-6 OR TNF-α OR adipokine OR cytokine). Forty-nine studies on adipocytokines have been included in this review. Adiponectin has been linked with anti-proliferative and anti-metastatic effects on endometrial cancer cells and is associated with a better prognosis. Leptin, visfatin and resistin are linked to the stimulation of endometrial cancer growth, proliferation, invasion and metastasis and are associated with worse prognosis or with a higher grade/stage of endometrial cancer. IL-6, Il-11, IL-31, IL-33, TNF-α, TGF-β1, SDF-1 and CXCR are involved in endometrial cancer cell growth and metastasis or involved in epithelial mesenchymal transformation (EMT) or associated with advanced disease. Adipocytokines have been found to directly impact endometrial cancer cell proliferation, invasion and migration. These molecules and their signalling pathways may be used to determine prognosis and course of the disease and may also be exploited as potential targets for cancer treatment and prevention of progression. Springer US 2021-12-24 2022 /pmc/articles/PMC8924097/ /pubmed/34951691 http://dx.doi.org/10.1007/s10555-021-10002-6 Text en © The Author(s) 2021, corrected publication 2022 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/) . |
spellingShingle | Clinical Ray, Irene Meira, Lisiane B. Michael, Agnieszka Ellis, Patricia E. Adipocytokines and disease progression in endometrial cancer: a systematic review |
title | Adipocytokines and disease progression in endometrial cancer: a systematic review |
title_full | Adipocytokines and disease progression in endometrial cancer: a systematic review |
title_fullStr | Adipocytokines and disease progression in endometrial cancer: a systematic review |
title_full_unstemmed | Adipocytokines and disease progression in endometrial cancer: a systematic review |
title_short | Adipocytokines and disease progression in endometrial cancer: a systematic review |
title_sort | adipocytokines and disease progression in endometrial cancer: a systematic review |
topic | Clinical |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924097/ https://www.ncbi.nlm.nih.gov/pubmed/34951691 http://dx.doi.org/10.1007/s10555-021-10002-6 |
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