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Cancer Cell Fusion: Mechanisms Slowly Unravel
Although molecular mechanisms and signaling pathways driving invasion and metastasis have been studied for many years, the origin of the population of metastatic cells within the primary tumor is still not well understood. About a century ago, Aichel proposed that cancer cell fusion was a mechanism...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037852/ https://www.ncbi.nlm.nih.gov/pubmed/27657058 http://dx.doi.org/10.3390/ijms17091587 |
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author | Noubissi, Felicite K. Ogle, Brenda M. |
author_facet | Noubissi, Felicite K. Ogle, Brenda M. |
author_sort | Noubissi, Felicite K. |
collection | PubMed |
description | Although molecular mechanisms and signaling pathways driving invasion and metastasis have been studied for many years, the origin of the population of metastatic cells within the primary tumor is still not well understood. About a century ago, Aichel proposed that cancer cell fusion was a mechanism of cancer metastasis. This hypothesis gained some support over the years, and recently became the focus of many studies that revealed increasing evidence pointing to the possibility that cancer cell fusion probably gives rise to the metastatic phenotype by generating widespread genetic and epigenetic diversity, leading to the emergence of critical populations needed to evolve resistance to the treatment and development of metastasis. In this review, we will discuss the clinical relevance of cancer cell fusion, describe emerging mechanisms of cancer cell fusion, address why inhibiting cancer cell fusion could represent a critical line of attack to limit drug resistance and to prevent metastasis, and suggest one new modality for doing so. |
format | Online Article Text |
id | pubmed-5037852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-50378522016-09-29 Cancer Cell Fusion: Mechanisms Slowly Unravel Noubissi, Felicite K. Ogle, Brenda M. Int J Mol Sci Review Although molecular mechanisms and signaling pathways driving invasion and metastasis have been studied for many years, the origin of the population of metastatic cells within the primary tumor is still not well understood. About a century ago, Aichel proposed that cancer cell fusion was a mechanism of cancer metastasis. This hypothesis gained some support over the years, and recently became the focus of many studies that revealed increasing evidence pointing to the possibility that cancer cell fusion probably gives rise to the metastatic phenotype by generating widespread genetic and epigenetic diversity, leading to the emergence of critical populations needed to evolve resistance to the treatment and development of metastasis. In this review, we will discuss the clinical relevance of cancer cell fusion, describe emerging mechanisms of cancer cell fusion, address why inhibiting cancer cell fusion could represent a critical line of attack to limit drug resistance and to prevent metastasis, and suggest one new modality for doing so. MDPI 2016-09-21 /pmc/articles/PMC5037852/ /pubmed/27657058 http://dx.doi.org/10.3390/ijms17091587 Text en © 2016 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 Noubissi, Felicite K. Ogle, Brenda M. Cancer Cell Fusion: Mechanisms Slowly Unravel |
title | Cancer Cell Fusion: Mechanisms Slowly Unravel |
title_full | Cancer Cell Fusion: Mechanisms Slowly Unravel |
title_fullStr | Cancer Cell Fusion: Mechanisms Slowly Unravel |
title_full_unstemmed | Cancer Cell Fusion: Mechanisms Slowly Unravel |
title_short | Cancer Cell Fusion: Mechanisms Slowly Unravel |
title_sort | cancer cell fusion: mechanisms slowly unravel |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037852/ https://www.ncbi.nlm.nih.gov/pubmed/27657058 http://dx.doi.org/10.3390/ijms17091587 |
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