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Tumor Hypoxia and Circulating Tumor Cells
Circulating tumor cells (CTCs) are a rare tumor cell subpopulation induced and selected by the tumor microenvironment’s extreme conditions. Under hypoxia and starvation, these aggressive and invasive cells are able to invade the lymphatic and circulatory systems. Escaping from the primary tumor, CTC...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766826/ https://www.ncbi.nlm.nih.gov/pubmed/33339353 http://dx.doi.org/10.3390/ijms21249592 |
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author | Tinganelli, Walter Durante, Marco |
author_facet | Tinganelli, Walter Durante, Marco |
author_sort | Tinganelli, Walter |
collection | PubMed |
description | Circulating tumor cells (CTCs) are a rare tumor cell subpopulation induced and selected by the tumor microenvironment’s extreme conditions. Under hypoxia and starvation, these aggressive and invasive cells are able to invade the lymphatic and circulatory systems. Escaping from the primary tumor, CTCs enter into the bloodstream to form metastatic deposits or re-establish themselves in cancer’s primary site. Although radiotherapy is widely used to cure solid malignancies, it can promote metastasis. Radiation can disrupt the primary tumor vasculature, increasing the dissemination of CTCs. Radiation also induces epithelial–mesenchymal transition (EMT) and eliminates suppressive signaling, causing the proliferation of existent, but previously dormant, disseminated tumor cells (DTCs). In this review, we collect the results and evidence underlying the molecular mechanisms of CTCs and DTCs and the effects of radiation and hypoxia in developing these cells. |
format | Online Article Text |
id | pubmed-7766826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77668262020-12-28 Tumor Hypoxia and Circulating Tumor Cells Tinganelli, Walter Durante, Marco Int J Mol Sci Review Circulating tumor cells (CTCs) are a rare tumor cell subpopulation induced and selected by the tumor microenvironment’s extreme conditions. Under hypoxia and starvation, these aggressive and invasive cells are able to invade the lymphatic and circulatory systems. Escaping from the primary tumor, CTCs enter into the bloodstream to form metastatic deposits or re-establish themselves in cancer’s primary site. Although radiotherapy is widely used to cure solid malignancies, it can promote metastasis. Radiation can disrupt the primary tumor vasculature, increasing the dissemination of CTCs. Radiation also induces epithelial–mesenchymal transition (EMT) and eliminates suppressive signaling, causing the proliferation of existent, but previously dormant, disseminated tumor cells (DTCs). In this review, we collect the results and evidence underlying the molecular mechanisms of CTCs and DTCs and the effects of radiation and hypoxia in developing these cells. MDPI 2020-12-16 /pmc/articles/PMC7766826/ /pubmed/33339353 http://dx.doi.org/10.3390/ijms21249592 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Tinganelli, Walter Durante, Marco Tumor Hypoxia and Circulating Tumor Cells |
title | Tumor Hypoxia and Circulating Tumor Cells |
title_full | Tumor Hypoxia and Circulating Tumor Cells |
title_fullStr | Tumor Hypoxia and Circulating Tumor Cells |
title_full_unstemmed | Tumor Hypoxia and Circulating Tumor Cells |
title_short | Tumor Hypoxia and Circulating Tumor Cells |
title_sort | tumor hypoxia and circulating tumor cells |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766826/ https://www.ncbi.nlm.nih.gov/pubmed/33339353 http://dx.doi.org/10.3390/ijms21249592 |
work_keys_str_mv | AT tinganelliwalter tumorhypoxiaandcirculatingtumorcells AT durantemarco tumorhypoxiaandcirculatingtumorcells |