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Clinical significance of phenotyping and karyotyping of circulating tumor cells in patients with advanced gastric cancer
BACKGROUND: Karyotyping and phenotyping of circulating tumor cells (CTCs) in therapeutic cancer patients is of particular clinical significance in terms of both identifying chemo-resistant CTC subtypes and understanding CTC evolution. METHODS: The integrated subtraction enrichment (SET) and immunost...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196148/ https://www.ncbi.nlm.nih.gov/pubmed/25026283 |
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author | Li, Yilin Zhang, Xiaotian Ge, Sai Gao, Jing Gong, Jifang Lu, Ming Zhang, Qiyue Cao, Yanshuo Wang, Daisy Dandan Lin, Peter Ping Shen, Lin |
author_facet | Li, Yilin Zhang, Xiaotian Ge, Sai Gao, Jing Gong, Jifang Lu, Ming Zhang, Qiyue Cao, Yanshuo Wang, Daisy Dandan Lin, Peter Ping Shen, Lin |
author_sort | Li, Yilin |
collection | PubMed |
description | BACKGROUND: Karyotyping and phenotyping of circulating tumor cells (CTCs) in therapeutic cancer patients is of particular clinical significance in terms of both identifying chemo-resistant CTC subtypes and understanding CTC evolution. METHODS: The integrated subtraction enrichment (SET) and immunostaining-fluorescence in situ hybridization (iFISH) platform was applied to detect and characterize CTCs in patients with advanced gastric cancer (AGC). Status of human epidermal growth factor receptor 2 (HER2) expressing and aneuploidy of chromosome 8 in CTCs enriched from the patients was examined by SET-iFISH following clinical chemotherapy or HER2-targeted therapy. CellSearch system was applied as a reference control. RESULTS: Phenotyping of CTCs in HER2 positive AGC patients demonstrated that HER2(+) CTCs could be effectively eliminated in response to HER2-targeted therapy. Karyotyping of CTCs indicated that distinct CTCs with different ploidies of chromosomes 8 in AGC patients correlated to either sensitivity or resistance of paclitaxel or cisplatin-based chemotherapy. Examination of the copy number of chromosome 8 in CTCs provides a potential approach for predicting chemotherapeutic efficacy and monitoring chemo-resistance. CONCLUSIONS: Phenotyping and karyotyping of the enriched CTCs upon ploidy of chromosome 8 or HER2 expression is of clinical potential for monitoring chemo-resistance and evaluating therapeutic efficacy for AGC patients. |
format | Online Article Text |
id | pubmed-4196148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-41961482014-10-21 Clinical significance of phenotyping and karyotyping of circulating tumor cells in patients with advanced gastric cancer Li, Yilin Zhang, Xiaotian Ge, Sai Gao, Jing Gong, Jifang Lu, Ming Zhang, Qiyue Cao, Yanshuo Wang, Daisy Dandan Lin, Peter Ping Shen, Lin Oncotarget Clinical Research Paper BACKGROUND: Karyotyping and phenotyping of circulating tumor cells (CTCs) in therapeutic cancer patients is of particular clinical significance in terms of both identifying chemo-resistant CTC subtypes and understanding CTC evolution. METHODS: The integrated subtraction enrichment (SET) and immunostaining-fluorescence in situ hybridization (iFISH) platform was applied to detect and characterize CTCs in patients with advanced gastric cancer (AGC). Status of human epidermal growth factor receptor 2 (HER2) expressing and aneuploidy of chromosome 8 in CTCs enriched from the patients was examined by SET-iFISH following clinical chemotherapy or HER2-targeted therapy. CellSearch system was applied as a reference control. RESULTS: Phenotyping of CTCs in HER2 positive AGC patients demonstrated that HER2(+) CTCs could be effectively eliminated in response to HER2-targeted therapy. Karyotyping of CTCs indicated that distinct CTCs with different ploidies of chromosomes 8 in AGC patients correlated to either sensitivity or resistance of paclitaxel or cisplatin-based chemotherapy. Examination of the copy number of chromosome 8 in CTCs provides a potential approach for predicting chemotherapeutic efficacy and monitoring chemo-resistance. CONCLUSIONS: Phenotyping and karyotyping of the enriched CTCs upon ploidy of chromosome 8 or HER2 expression is of clinical potential for monitoring chemo-resistance and evaluating therapeutic efficacy for AGC patients. Impact Journals LLC 2014-07-07 /pmc/articles/PMC4196148/ /pubmed/25026283 Text en Copyright: © 2014 Li et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Clinical Research Paper Li, Yilin Zhang, Xiaotian Ge, Sai Gao, Jing Gong, Jifang Lu, Ming Zhang, Qiyue Cao, Yanshuo Wang, Daisy Dandan Lin, Peter Ping Shen, Lin Clinical significance of phenotyping and karyotyping of circulating tumor cells in patients with advanced gastric cancer |
title | Clinical significance of phenotyping and karyotyping of circulating tumor cells in patients with advanced gastric cancer |
title_full | Clinical significance of phenotyping and karyotyping of circulating tumor cells in patients with advanced gastric cancer |
title_fullStr | Clinical significance of phenotyping and karyotyping of circulating tumor cells in patients with advanced gastric cancer |
title_full_unstemmed | Clinical significance of phenotyping and karyotyping of circulating tumor cells in patients with advanced gastric cancer |
title_short | Clinical significance of phenotyping and karyotyping of circulating tumor cells in patients with advanced gastric cancer |
title_sort | clinical significance of phenotyping and karyotyping of circulating tumor cells in patients with advanced gastric cancer |
topic | Clinical Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196148/ https://www.ncbi.nlm.nih.gov/pubmed/25026283 |
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