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Relationship of tumor marker CA125 and ovarian tumor stem cells: preliminary identification
PURPOSE: The purpose of this study is to identify a prospective association between CA125 and tumorigenic ovarian cancer cells, using the new method of orthotopic transplantation (1). METHOD: After making the surgical ovarian cancer specimen into cell suspension, we separated the tumorigenic cells f...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383191/ https://www.ncbi.nlm.nih.gov/pubmed/25886959 http://dx.doi.org/10.1186/s13048-015-0132-8 |
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author | Zhang, Hui Yang, Yongan Wang, Yifeng Gao, Xinping Wang, Weiming Liu, Hui He, Haipeng Liang, Yijuan Pan, Kun Wu, Hongli Shi, Junrong Xue, Huiling Liang, Ling Cai, Zhihuci Fan, Yanfang Zhang, Yanyan |
author_facet | Zhang, Hui Yang, Yongan Wang, Yifeng Gao, Xinping Wang, Weiming Liu, Hui He, Haipeng Liang, Yijuan Pan, Kun Wu, Hongli Shi, Junrong Xue, Huiling Liang, Ling Cai, Zhihuci Fan, Yanfang Zhang, Yanyan |
author_sort | Zhang, Hui |
collection | PubMed |
description | PURPOSE: The purpose of this study is to identify a prospective association between CA125 and tumorigenic ovarian cancer cells, using the new method of orthotopic transplantation (1). METHOD: After making the surgical ovarian cancer specimen into cell suspension, we separated the tumorigenic cells from the nontumorigenic cancer cells based on cell surface marker (cancer antigen CA125 and lineage markers) expression. We developed a SCID mice model in which the CA125+/ lineage- and CA125-/ lineage- cells were injected into ovarian parenchyma by use of a microinjector. As a measure of effectiveness of tumor-forming, tumor weight, abdominal distension, ascites volume and activity, subcutaneous fat were determined or observed. Immunohistochemistry was done to determine tumor cell markers. RESULTS: We found that the cells of CA125+/ lineage- were able to form new tumors; whereas, an equal quantity of CA125-/lineage- cells failed to form any tumors. The new generated tumor contained additional CA125-/lineage- tumorigenic cells as well as the phenotypically diverse population of nontumorigenic cells. Quantities were judged to be significantly different P < 0.0001. CONCLUSION: CA125+/ lineage- cells, which may be ovarian cancer stem cells, were the source for tumor recurrence. The strategies designed to target this cell population may lead to more effective therapies. |
format | Online Article Text |
id | pubmed-4383191 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43831912015-04-03 Relationship of tumor marker CA125 and ovarian tumor stem cells: preliminary identification Zhang, Hui Yang, Yongan Wang, Yifeng Gao, Xinping Wang, Weiming Liu, Hui He, Haipeng Liang, Yijuan Pan, Kun Wu, Hongli Shi, Junrong Xue, Huiling Liang, Ling Cai, Zhihuci Fan, Yanfang Zhang, Yanyan J Ovarian Res Research PURPOSE: The purpose of this study is to identify a prospective association between CA125 and tumorigenic ovarian cancer cells, using the new method of orthotopic transplantation (1). METHOD: After making the surgical ovarian cancer specimen into cell suspension, we separated the tumorigenic cells from the nontumorigenic cancer cells based on cell surface marker (cancer antigen CA125 and lineage markers) expression. We developed a SCID mice model in which the CA125+/ lineage- and CA125-/ lineage- cells were injected into ovarian parenchyma by use of a microinjector. As a measure of effectiveness of tumor-forming, tumor weight, abdominal distension, ascites volume and activity, subcutaneous fat were determined or observed. Immunohistochemistry was done to determine tumor cell markers. RESULTS: We found that the cells of CA125+/ lineage- were able to form new tumors; whereas, an equal quantity of CA125-/lineage- cells failed to form any tumors. The new generated tumor contained additional CA125-/lineage- tumorigenic cells as well as the phenotypically diverse population of nontumorigenic cells. Quantities were judged to be significantly different P < 0.0001. CONCLUSION: CA125+/ lineage- cells, which may be ovarian cancer stem cells, were the source for tumor recurrence. The strategies designed to target this cell population may lead to more effective therapies. BioMed Central 2015-03-28 /pmc/articles/PMC4383191/ /pubmed/25886959 http://dx.doi.org/10.1186/s13048-015-0132-8 Text en © Zhang et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Zhang, Hui Yang, Yongan Wang, Yifeng Gao, Xinping Wang, Weiming Liu, Hui He, Haipeng Liang, Yijuan Pan, Kun Wu, Hongli Shi, Junrong Xue, Huiling Liang, Ling Cai, Zhihuci Fan, Yanfang Zhang, Yanyan Relationship of tumor marker CA125 and ovarian tumor stem cells: preliminary identification |
title | Relationship of tumor marker CA125 and ovarian tumor stem cells: preliminary identification |
title_full | Relationship of tumor marker CA125 and ovarian tumor stem cells: preliminary identification |
title_fullStr | Relationship of tumor marker CA125 and ovarian tumor stem cells: preliminary identification |
title_full_unstemmed | Relationship of tumor marker CA125 and ovarian tumor stem cells: preliminary identification |
title_short | Relationship of tumor marker CA125 and ovarian tumor stem cells: preliminary identification |
title_sort | relationship of tumor marker ca125 and ovarian tumor stem cells: preliminary identification |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383191/ https://www.ncbi.nlm.nih.gov/pubmed/25886959 http://dx.doi.org/10.1186/s13048-015-0132-8 |
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