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Occurrence of cancer at multiple sites: Towards distinguishing multigenesis from metastasis

BACKGROUND: Occurrence of tumors at multiple sites is a hallmark of malignant cancers and contributes to the high mortality of cancers. The formation of multi-site cancers (MSCs) has conventionally been regarded as a result of hematogenous metastasis. However, some MSCs may appear as unusual in the...

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Autores principales: Zhang, Wei-Kang, Zhang, Chun, Zhang, Jing J, Liu, Shi V
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2373780/
https://www.ncbi.nlm.nih.gov/pubmed/18405362
http://dx.doi.org/10.1186/1745-6150-3-14
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author Zhang, Wei-Kang
Zhang, Chun
Zhang, Jing J
Liu, Shi V
author_facet Zhang, Wei-Kang
Zhang, Chun
Zhang, Jing J
Liu, Shi V
author_sort Zhang, Wei-Kang
collection PubMed
description BACKGROUND: Occurrence of tumors at multiple sites is a hallmark of malignant cancers and contributes to the high mortality of cancers. The formation of multi-site cancers (MSCs) has conventionally been regarded as a result of hematogenous metastasis. However, some MSCs may appear as unusual in the sense of vascular dissemination pattern and therefore be explained by alternative metastasis models or even by non-metastatic independent formation mechanisms. RESULTS: Through literature review and incorporation of recent advance in understanding aging and development, we identified two alternative mechanisms for the independent formation of MSCs: 1) formation of separate tumors from cancer-initiating cells (CICs) mutated at an early stage of development and then diverging as to their physical locations upon further development, 2) formation of separate tumors from different CICs that contain mutations in some convergent ways. Either of these processes does not require long-distance migration and/or vascular dissemination of cancer cells from a primary site to a secondary site. Thus, we classify the formation of these MSCs from indigenous CICs (iCICs) into a new mechanistic category of tumor formation – multigenesis. CONCLUSION: A multigenesis view on multi-site cancer (MSCs) may offer explanations for some "unusual metastasis" and has important implications for designing expanded strategies for the diagnosis and treatment of cancers. REVIEWERS: This article was reviewed by Carlo C. Maley nominated by Laura F. Landweber and Razvan T. Radulescu nominated by David R. Kaplan. For the full reviews, please go to the Reviewers' comments section.
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spelling pubmed-23737802008-05-08 Occurrence of cancer at multiple sites: Towards distinguishing multigenesis from metastasis Zhang, Wei-Kang Zhang, Chun Zhang, Jing J Liu, Shi V Biol Direct Hypothesis BACKGROUND: Occurrence of tumors at multiple sites is a hallmark of malignant cancers and contributes to the high mortality of cancers. The formation of multi-site cancers (MSCs) has conventionally been regarded as a result of hematogenous metastasis. However, some MSCs may appear as unusual in the sense of vascular dissemination pattern and therefore be explained by alternative metastasis models or even by non-metastatic independent formation mechanisms. RESULTS: Through literature review and incorporation of recent advance in understanding aging and development, we identified two alternative mechanisms for the independent formation of MSCs: 1) formation of separate tumors from cancer-initiating cells (CICs) mutated at an early stage of development and then diverging as to their physical locations upon further development, 2) formation of separate tumors from different CICs that contain mutations in some convergent ways. Either of these processes does not require long-distance migration and/or vascular dissemination of cancer cells from a primary site to a secondary site. Thus, we classify the formation of these MSCs from indigenous CICs (iCICs) into a new mechanistic category of tumor formation – multigenesis. CONCLUSION: A multigenesis view on multi-site cancer (MSCs) may offer explanations for some "unusual metastasis" and has important implications for designing expanded strategies for the diagnosis and treatment of cancers. REVIEWERS: This article was reviewed by Carlo C. Maley nominated by Laura F. Landweber and Razvan T. Radulescu nominated by David R. Kaplan. For the full reviews, please go to the Reviewers' comments section. BioMed Central 2008-04-11 /pmc/articles/PMC2373780/ /pubmed/18405362 http://dx.doi.org/10.1186/1745-6150-3-14 Text en Copyright © 2008 Zhang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Hypothesis
Zhang, Wei-Kang
Zhang, Chun
Zhang, Jing J
Liu, Shi V
Occurrence of cancer at multiple sites: Towards distinguishing multigenesis from metastasis
title Occurrence of cancer at multiple sites: Towards distinguishing multigenesis from metastasis
title_full Occurrence of cancer at multiple sites: Towards distinguishing multigenesis from metastasis
title_fullStr Occurrence of cancer at multiple sites: Towards distinguishing multigenesis from metastasis
title_full_unstemmed Occurrence of cancer at multiple sites: Towards distinguishing multigenesis from metastasis
title_short Occurrence of cancer at multiple sites: Towards distinguishing multigenesis from metastasis
title_sort occurrence of cancer at multiple sites: towards distinguishing multigenesis from metastasis
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2373780/
https://www.ncbi.nlm.nih.gov/pubmed/18405362
http://dx.doi.org/10.1186/1745-6150-3-14
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