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A Specific Common Chromosomal Pathway for the Origin of Human Malignancy—II

A consistent chromosome abnormality exists in 17 human cell lines and in 11 fresh cancers, a finding strongly supportive of our original support of Boveri's concept of a chromosomal imbalance origin of human cancer. This abnormality is in the form of a marked excess of E16 chromosomes per cell,...

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Detalles Bibliográficos
Autores principales: Minkler, J. L., Gofman, J. W., Tandy, R. K.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1970
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2008712/
https://www.ncbi.nlm.nih.gov/pubmed/4323224
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author Minkler, J. L.
Gofman, J. W.
Tandy, R. K.
author_facet Minkler, J. L.
Gofman, J. W.
Tandy, R. K.
author_sort Minkler, J. L.
collection PubMed
description A consistent chromosome abnormality exists in 17 human cell lines and in 11 fresh cancers, a finding strongly supportive of our original support of Boveri's concept of a chromosomal imbalance origin of human cancer. This abnormality is in the form of a marked excess of E16 chromosomes per cell, either absolute or in relationship to other chromosome classes. If the ratio of E16 chromosomes to those of other classes be the crucial parameter, several ratios involving E16 chromosomes must be considered as candidates. We feel the choice between such possible ratios might be better made when 100 or more human cancers have been studied, rather than now. It may be that imbalance in E16 chromosomes relative to certain other classes represents a necessary condition for malignant cell behavior, but that more than one such E16 imbalance may be a sufficient condition.
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spelling pubmed-20087122009-09-10 A Specific Common Chromosomal Pathway for the Origin of Human Malignancy—II Minkler, J. L. Gofman, J. W. Tandy, R. K. Br J Cancer Articles A consistent chromosome abnormality exists in 17 human cell lines and in 11 fresh cancers, a finding strongly supportive of our original support of Boveri's concept of a chromosomal imbalance origin of human cancer. This abnormality is in the form of a marked excess of E16 chromosomes per cell, either absolute or in relationship to other chromosome classes. If the ratio of E16 chromosomes to those of other classes be the crucial parameter, several ratios involving E16 chromosomes must be considered as candidates. We feel the choice between such possible ratios might be better made when 100 or more human cancers have been studied, rather than now. It may be that imbalance in E16 chromosomes relative to certain other classes represents a necessary condition for malignant cell behavior, but that more than one such E16 imbalance may be a sufficient condition. Nature Publishing Group 1970-12 /pmc/articles/PMC2008712/ /pubmed/4323224 Text en https://creativecommons.org/licenses/by/4.0/This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Articles
Minkler, J. L.
Gofman, J. W.
Tandy, R. K.
A Specific Common Chromosomal Pathway for the Origin of Human Malignancy—II
title A Specific Common Chromosomal Pathway for the Origin of Human Malignancy—II
title_full A Specific Common Chromosomal Pathway for the Origin of Human Malignancy—II
title_fullStr A Specific Common Chromosomal Pathway for the Origin of Human Malignancy—II
title_full_unstemmed A Specific Common Chromosomal Pathway for the Origin of Human Malignancy—II
title_short A Specific Common Chromosomal Pathway for the Origin of Human Malignancy—II
title_sort specific common chromosomal pathway for the origin of human malignancy—ii
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2008712/
https://www.ncbi.nlm.nih.gov/pubmed/4323224
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