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Colorectal Cancer with Residual Polyp of Origin: A Model of Malignant Transformation()()
The majority of colorectal cancers (CRCs) arise from adenomatous polyps. In this study, we sought to present the underrecognized CRC with the residual polyp of origin (CRC RPO +) as an entity to be utilized as a model to study colorectal carcinogenesis. We identified all subjects with biopsy-proven...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Neoplasia Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941582/ https://www.ncbi.nlm.nih.gov/pubmed/27567950 http://dx.doi.org/10.1016/j.tranon.2016.06.002 |
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author | Druliner, Brooke R. Rashtak, Shahrooz Ruan, Xiaoyang Bae, Taejeong Vasmatzis, Nikolaos O’Brien, Daniel Johnson, Ruth Felmlee-Devine, Donna Washechek-Aletto, Jill Basu, Nivedita Liu, Hongfang Smyrk, Thomas Abyzov, Alexej Boardman, Lisa A. |
author_facet | Druliner, Brooke R. Rashtak, Shahrooz Ruan, Xiaoyang Bae, Taejeong Vasmatzis, Nikolaos O’Brien, Daniel Johnson, Ruth Felmlee-Devine, Donna Washechek-Aletto, Jill Basu, Nivedita Liu, Hongfang Smyrk, Thomas Abyzov, Alexej Boardman, Lisa A. |
author_sort | Druliner, Brooke R. |
collection | PubMed |
description | The majority of colorectal cancers (CRCs) arise from adenomatous polyps. In this study, we sought to present the underrecognized CRC with the residual polyp of origin (CRC RPO +) as an entity to be utilized as a model to study colorectal carcinogenesis. We identified all subjects with biopsy-proven CRC RPO + that were evaluated over 10 years at Mayo Clinic, Rochester, MN, and compared their clinical and pathologic characteristics to CRC without remnant polyps (CRC RPO −). Overall survival and disease-free survival overlap with an equivalent hazard ratio between CRC RPO + and RPO − cases when age, stage, and grade are adjusted. The somatic genomic profile obtained by whole genome sequencing and the gene expression profiles by RNA-seq for CRC RPO + tumors were compared with that of age -and gender-matched CRC RPO − evaluated by The Cancer Genome Atlas. CRC RPO + cases were more commonly found with lower-grade, earlier-stage disease than CRC RPO −. However, within the same disease stage and grade, their clinical course is very similar to that of CRC RPO −. The mutation frequencies of commonly mutated genes in CRC are similar between CRC RPO + and RPO − cases. Likewise, gene expression patterns are indistinguishable between the RPO + and RPO − cases. We have confirmed that CRC RPO + is clinically and biologically similar to CRC RPO − and may be utilized as a model of the adenoma to carcinoma transition. |
format | Online Article Text |
id | pubmed-4941582 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Neoplasia Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49415822016-07-13 Colorectal Cancer with Residual Polyp of Origin: A Model of Malignant Transformation()() Druliner, Brooke R. Rashtak, Shahrooz Ruan, Xiaoyang Bae, Taejeong Vasmatzis, Nikolaos O’Brien, Daniel Johnson, Ruth Felmlee-Devine, Donna Washechek-Aletto, Jill Basu, Nivedita Liu, Hongfang Smyrk, Thomas Abyzov, Alexej Boardman, Lisa A. Transl Oncol Original article The majority of colorectal cancers (CRCs) arise from adenomatous polyps. In this study, we sought to present the underrecognized CRC with the residual polyp of origin (CRC RPO +) as an entity to be utilized as a model to study colorectal carcinogenesis. We identified all subjects with biopsy-proven CRC RPO + that were evaluated over 10 years at Mayo Clinic, Rochester, MN, and compared their clinical and pathologic characteristics to CRC without remnant polyps (CRC RPO −). Overall survival and disease-free survival overlap with an equivalent hazard ratio between CRC RPO + and RPO − cases when age, stage, and grade are adjusted. The somatic genomic profile obtained by whole genome sequencing and the gene expression profiles by RNA-seq for CRC RPO + tumors were compared with that of age -and gender-matched CRC RPO − evaluated by The Cancer Genome Atlas. CRC RPO + cases were more commonly found with lower-grade, earlier-stage disease than CRC RPO −. However, within the same disease stage and grade, their clinical course is very similar to that of CRC RPO −. The mutation frequencies of commonly mutated genes in CRC are similar between CRC RPO + and RPO − cases. Likewise, gene expression patterns are indistinguishable between the RPO + and RPO − cases. We have confirmed that CRC RPO + is clinically and biologically similar to CRC RPO − and may be utilized as a model of the adenoma to carcinoma transition. Neoplasia Press 2016-07-09 /pmc/articles/PMC4941582/ /pubmed/27567950 http://dx.doi.org/10.1016/j.tranon.2016.06.002 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original article Druliner, Brooke R. Rashtak, Shahrooz Ruan, Xiaoyang Bae, Taejeong Vasmatzis, Nikolaos O’Brien, Daniel Johnson, Ruth Felmlee-Devine, Donna Washechek-Aletto, Jill Basu, Nivedita Liu, Hongfang Smyrk, Thomas Abyzov, Alexej Boardman, Lisa A. Colorectal Cancer with Residual Polyp of Origin: A Model of Malignant Transformation()() |
title | Colorectal Cancer with Residual Polyp of Origin: A Model of Malignant Transformation()() |
title_full | Colorectal Cancer with Residual Polyp of Origin: A Model of Malignant Transformation()() |
title_fullStr | Colorectal Cancer with Residual Polyp of Origin: A Model of Malignant Transformation()() |
title_full_unstemmed | Colorectal Cancer with Residual Polyp of Origin: A Model of Malignant Transformation()() |
title_short | Colorectal Cancer with Residual Polyp of Origin: A Model of Malignant Transformation()() |
title_sort | colorectal cancer with residual polyp of origin: a model of malignant transformation()() |
topic | Original article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941582/ https://www.ncbi.nlm.nih.gov/pubmed/27567950 http://dx.doi.org/10.1016/j.tranon.2016.06.002 |
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