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Lineage relationship of prostate cancer cell types based on gene expression

BACKGROUND: Prostate tumor heterogeneity is a major factor in disease management. Heterogeneity could be due to multiple cancer cell types with distinct gene expression. Of clinical importance is the so-called cancer stem cell type. Cell type-specific transcriptomes are used to examine lineage relat...

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Autores principales: Pascal, Laura E, Vêncio, Ricardo ZN, Vessella, Robert L, Ware, Carol B, Vêncio, Eneida F, Denyer, Gareth, Liu, Alvin Y
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3113924/
https://www.ncbi.nlm.nih.gov/pubmed/21605402
http://dx.doi.org/10.1186/1755-8794-4-46
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author Pascal, Laura E
Vêncio, Ricardo ZN
Vessella, Robert L
Ware, Carol B
Vêncio, Eneida F
Denyer, Gareth
Liu, Alvin Y
author_facet Pascal, Laura E
Vêncio, Ricardo ZN
Vessella, Robert L
Ware, Carol B
Vêncio, Eneida F
Denyer, Gareth
Liu, Alvin Y
author_sort Pascal, Laura E
collection PubMed
description BACKGROUND: Prostate tumor heterogeneity is a major factor in disease management. Heterogeneity could be due to multiple cancer cell types with distinct gene expression. Of clinical importance is the so-called cancer stem cell type. Cell type-specific transcriptomes are used to examine lineage relationship among cancer cell types and their expression similarity to normal cell types including stem/progenitor cells. METHODS: Transcriptomes were determined by Affymetrix DNA array analysis for the following cell types. Putative prostate progenitor cell populations were characterized and isolated by expression of the membrane transporter ABCG2. Stem cells were represented by embryonic stem and embryonal carcinoma cells. The cancer cell types were Gleason pattern 3 (glandular histomorphology) and pattern 4 (aglandular) sorted from primary tumors, cultured prostate cancer cell lines originally established from metastatic lesions, xenografts LuCaP 35 (adenocarcinoma phenotype) and LuCaP 49 (neuroendocrine/small cell carcinoma) grown in mice. No detectable gene expression differences were detected among serial passages of the LuCaP xenografts. RESULTS: Based on transcriptomes, the different cancer cell types could be clustered into a luminal-like grouping and a non-luminal-like (also not basal-like) grouping. The non-luminal-like types showed expression more similar to that of stem/progenitor cells than the luminal-like types. However, none showed expression of stem cell genes known to maintain stemness. CONCLUSIONS: Non-luminal-like types are all representatives of aggressive disease, and this could be attributed to the similarity in overall gene expression to stem and progenitor cell types.
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spelling pubmed-31139242011-06-14 Lineage relationship of prostate cancer cell types based on gene expression Pascal, Laura E Vêncio, Ricardo ZN Vessella, Robert L Ware, Carol B Vêncio, Eneida F Denyer, Gareth Liu, Alvin Y BMC Med Genomics Research Article BACKGROUND: Prostate tumor heterogeneity is a major factor in disease management. Heterogeneity could be due to multiple cancer cell types with distinct gene expression. Of clinical importance is the so-called cancer stem cell type. Cell type-specific transcriptomes are used to examine lineage relationship among cancer cell types and their expression similarity to normal cell types including stem/progenitor cells. METHODS: Transcriptomes were determined by Affymetrix DNA array analysis for the following cell types. Putative prostate progenitor cell populations were characterized and isolated by expression of the membrane transporter ABCG2. Stem cells were represented by embryonic stem and embryonal carcinoma cells. The cancer cell types were Gleason pattern 3 (glandular histomorphology) and pattern 4 (aglandular) sorted from primary tumors, cultured prostate cancer cell lines originally established from metastatic lesions, xenografts LuCaP 35 (adenocarcinoma phenotype) and LuCaP 49 (neuroendocrine/small cell carcinoma) grown in mice. No detectable gene expression differences were detected among serial passages of the LuCaP xenografts. RESULTS: Based on transcriptomes, the different cancer cell types could be clustered into a luminal-like grouping and a non-luminal-like (also not basal-like) grouping. The non-luminal-like types showed expression more similar to that of stem/progenitor cells than the luminal-like types. However, none showed expression of stem cell genes known to maintain stemness. CONCLUSIONS: Non-luminal-like types are all representatives of aggressive disease, and this could be attributed to the similarity in overall gene expression to stem and progenitor cell types. BioMed Central 2011-05-23 /pmc/articles/PMC3113924/ /pubmed/21605402 http://dx.doi.org/10.1186/1755-8794-4-46 Text en Copyright ©2011 Pascal 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 Research Article
Pascal, Laura E
Vêncio, Ricardo ZN
Vessella, Robert L
Ware, Carol B
Vêncio, Eneida F
Denyer, Gareth
Liu, Alvin Y
Lineage relationship of prostate cancer cell types based on gene expression
title Lineage relationship of prostate cancer cell types based on gene expression
title_full Lineage relationship of prostate cancer cell types based on gene expression
title_fullStr Lineage relationship of prostate cancer cell types based on gene expression
title_full_unstemmed Lineage relationship of prostate cancer cell types based on gene expression
title_short Lineage relationship of prostate cancer cell types based on gene expression
title_sort lineage relationship of prostate cancer cell types based on gene expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3113924/
https://www.ncbi.nlm.nih.gov/pubmed/21605402
http://dx.doi.org/10.1186/1755-8794-4-46
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