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Cellular origin of bladder neoplasia and tissue dynamics of its progression to invasive carcinoma

Understanding how malignancies arise within normal tissues requires identification of the cancer cell of origin and knowledge of the cellular and tissue dynamics of tumor progression. Here we examine bladder cancer in a chemical carcinogenesis model that mimics muscle-invasive human bladder cancer....

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Detalles Bibliográficos
Autores principales: Shin, Kunyoo, Lim, Agnes, Odegaard, Justin I., Honeycutt, Jared D., Kawano, Sally, Hsieh, Michael H., Beachy, Philip A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196946/
https://www.ncbi.nlm.nih.gov/pubmed/24747439
http://dx.doi.org/10.1038/ncb2956
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author Shin, Kunyoo
Lim, Agnes
Odegaard, Justin I.
Honeycutt, Jared D.
Kawano, Sally
Hsieh, Michael H.
Beachy, Philip A.
author_facet Shin, Kunyoo
Lim, Agnes
Odegaard, Justin I.
Honeycutt, Jared D.
Kawano, Sally
Hsieh, Michael H.
Beachy, Philip A.
author_sort Shin, Kunyoo
collection PubMed
description Understanding how malignancies arise within normal tissues requires identification of the cancer cell of origin and knowledge of the cellular and tissue dynamics of tumor progression. Here we examine bladder cancer in a chemical carcinogenesis model that mimics muscle-invasive human bladder cancer. With no prior bias regarding genetic pathways or cell types, we prospectively mark or ablate cells to show that muscle-invasive bladder carcinomas arise exclusively from Sonic hedgehog (Shh)-expressing stem cells in basal urothelium. These carcinomas arise clonally from a single cell whose progeny aggressively colonize a major portion of the urothelium to generate a lesion with histological features identical to human carcinoma-in-situ. Shh-expressing basal cells within this precursor lesion become tumor-initiating cells, although Shh expression is lost in subsequent carcinomas. We thus find that invasive carcinoma is initiated from basal urothelial stem cells but that tumor cell phenotype can diverge significantly from that of the cancer cell-of-origin.
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spelling pubmed-41969462014-11-01 Cellular origin of bladder neoplasia and tissue dynamics of its progression to invasive carcinoma Shin, Kunyoo Lim, Agnes Odegaard, Justin I. Honeycutt, Jared D. Kawano, Sally Hsieh, Michael H. Beachy, Philip A. Nat Cell Biol Article Understanding how malignancies arise within normal tissues requires identification of the cancer cell of origin and knowledge of the cellular and tissue dynamics of tumor progression. Here we examine bladder cancer in a chemical carcinogenesis model that mimics muscle-invasive human bladder cancer. With no prior bias regarding genetic pathways or cell types, we prospectively mark or ablate cells to show that muscle-invasive bladder carcinomas arise exclusively from Sonic hedgehog (Shh)-expressing stem cells in basal urothelium. These carcinomas arise clonally from a single cell whose progeny aggressively colonize a major portion of the urothelium to generate a lesion with histological features identical to human carcinoma-in-situ. Shh-expressing basal cells within this precursor lesion become tumor-initiating cells, although Shh expression is lost in subsequent carcinomas. We thus find that invasive carcinoma is initiated from basal urothelial stem cells but that tumor cell phenotype can diverge significantly from that of the cancer cell-of-origin. 2014-04-20 2014-05 /pmc/articles/PMC4196946/ /pubmed/24747439 http://dx.doi.org/10.1038/ncb2956 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Shin, Kunyoo
Lim, Agnes
Odegaard, Justin I.
Honeycutt, Jared D.
Kawano, Sally
Hsieh, Michael H.
Beachy, Philip A.
Cellular origin of bladder neoplasia and tissue dynamics of its progression to invasive carcinoma
title Cellular origin of bladder neoplasia and tissue dynamics of its progression to invasive carcinoma
title_full Cellular origin of bladder neoplasia and tissue dynamics of its progression to invasive carcinoma
title_fullStr Cellular origin of bladder neoplasia and tissue dynamics of its progression to invasive carcinoma
title_full_unstemmed Cellular origin of bladder neoplasia and tissue dynamics of its progression to invasive carcinoma
title_short Cellular origin of bladder neoplasia and tissue dynamics of its progression to invasive carcinoma
title_sort cellular origin of bladder neoplasia and tissue dynamics of its progression to invasive carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196946/
https://www.ncbi.nlm.nih.gov/pubmed/24747439
http://dx.doi.org/10.1038/ncb2956
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