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Circulating tumor cells as a prognostic and predictive marker in gastrointestinal stromal tumors: a prospective study

BACKGROUND: Circulating tumor cells (CTC) are prognostic and predictive for several cancer types. Only limited data exist regarding prognostic or predictive impact of CTC on gastrointestinal stromal tumor (GIST) patients. The aim of our study was to elucidate the role of CTC in GIST patients. RESULT...

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Autores principales: Li, Qiang, Zhi, Xiaofei, Zhou, Jianping, Tao, Ran, Zhang, Jiaxuan, Chen, Peisheng, Røe, Oluf Dimitri, Sun, Luning, Ma, Lilin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095028/
https://www.ncbi.nlm.nih.gov/pubmed/27153560
http://dx.doi.org/10.18632/oncotarget.9128
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author Li, Qiang
Zhi, Xiaofei
Zhou, Jianping
Tao, Ran
Zhang, Jiaxuan
Chen, Peisheng
Røe, Oluf Dimitri
Sun, Luning
Ma, Lilin
author_facet Li, Qiang
Zhi, Xiaofei
Zhou, Jianping
Tao, Ran
Zhang, Jiaxuan
Chen, Peisheng
Røe, Oluf Dimitri
Sun, Luning
Ma, Lilin
author_sort Li, Qiang
collection PubMed
description BACKGROUND: Circulating tumor cells (CTC) are prognostic and predictive for several cancer types. Only limited data exist regarding prognostic or predictive impact of CTC on gastrointestinal stromal tumor (GIST) patients. The aim of our study was to elucidate the role of CTC in GIST patients. RESULTS: A total of 121 GIST patients and 54 non-GIST samples were enrolled in the study. The cutoff value for ANO1 positive was 3*10(−5) and 65 (54%) GIST patients were defined as ANO1 positive. ANO1s were more frequently detected in unresectable patients. Tumor size, mitotic count and risk level were associated with ANO1 detection in resectable GIST patients. The presence of ANO1 significantly correlated with poor disease-free survival (15.3 versus 19.6 months, p = 0.038). Most patients turned ANO1-negative after surgery and inversely, all 21 patients with recurrence turned ANO1-positive with high ANO1 expression levels. Moreover, in the neoadjuvant setting, decline of ANO1 expression level correlated with the response of imatinib. METHODS: Cells from peripheral blood mononuclear cells tested positive for anoctamin 1, calcium activated chloride channel, ANO1 (DOG1) were considered as tumor CTC of GISTs. The expression levels of ANO1 were determined using quantitative real-time polymerase chain reaction (qRT-PCR). The highest level of ANO1 expression in non-GIST samples was used as the “cutoff” value. CONCLUSION: ANO1 detection by qRT-PCR in peripheral blood is of clinical potential for monitoring recurrence and evaluating therapeutic efficacy of imatinib for GIST patients.
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spelling pubmed-50950282016-11-22 Circulating tumor cells as a prognostic and predictive marker in gastrointestinal stromal tumors: a prospective study Li, Qiang Zhi, Xiaofei Zhou, Jianping Tao, Ran Zhang, Jiaxuan Chen, Peisheng Røe, Oluf Dimitri Sun, Luning Ma, Lilin Oncotarget Research Paper BACKGROUND: Circulating tumor cells (CTC) are prognostic and predictive for several cancer types. Only limited data exist regarding prognostic or predictive impact of CTC on gastrointestinal stromal tumor (GIST) patients. The aim of our study was to elucidate the role of CTC in GIST patients. RESULTS: A total of 121 GIST patients and 54 non-GIST samples were enrolled in the study. The cutoff value for ANO1 positive was 3*10(−5) and 65 (54%) GIST patients were defined as ANO1 positive. ANO1s were more frequently detected in unresectable patients. Tumor size, mitotic count and risk level were associated with ANO1 detection in resectable GIST patients. The presence of ANO1 significantly correlated with poor disease-free survival (15.3 versus 19.6 months, p = 0.038). Most patients turned ANO1-negative after surgery and inversely, all 21 patients with recurrence turned ANO1-positive with high ANO1 expression levels. Moreover, in the neoadjuvant setting, decline of ANO1 expression level correlated with the response of imatinib. METHODS: Cells from peripheral blood mononuclear cells tested positive for anoctamin 1, calcium activated chloride channel, ANO1 (DOG1) were considered as tumor CTC of GISTs. The expression levels of ANO1 were determined using quantitative real-time polymerase chain reaction (qRT-PCR). The highest level of ANO1 expression in non-GIST samples was used as the “cutoff” value. CONCLUSION: ANO1 detection by qRT-PCR in peripheral blood is of clinical potential for monitoring recurrence and evaluating therapeutic efficacy of imatinib for GIST patients. Impact Journals LLC 2016-05-02 /pmc/articles/PMC5095028/ /pubmed/27153560 http://dx.doi.org/10.18632/oncotarget.9128 Text en Copyright: © 2016 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 Research Paper
Li, Qiang
Zhi, Xiaofei
Zhou, Jianping
Tao, Ran
Zhang, Jiaxuan
Chen, Peisheng
Røe, Oluf Dimitri
Sun, Luning
Ma, Lilin
Circulating tumor cells as a prognostic and predictive marker in gastrointestinal stromal tumors: a prospective study
title Circulating tumor cells as a prognostic and predictive marker in gastrointestinal stromal tumors: a prospective study
title_full Circulating tumor cells as a prognostic and predictive marker in gastrointestinal stromal tumors: a prospective study
title_fullStr Circulating tumor cells as a prognostic and predictive marker in gastrointestinal stromal tumors: a prospective study
title_full_unstemmed Circulating tumor cells as a prognostic and predictive marker in gastrointestinal stromal tumors: a prospective study
title_short Circulating tumor cells as a prognostic and predictive marker in gastrointestinal stromal tumors: a prospective study
title_sort circulating tumor cells as a prognostic and predictive marker in gastrointestinal stromal tumors: a prospective study
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095028/
https://www.ncbi.nlm.nih.gov/pubmed/27153560
http://dx.doi.org/10.18632/oncotarget.9128
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