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预测贝伐珠单抗抗肿瘤治疗效果的生物学标记物

Bevacizumab, the monoclonal antibody of vascular endothelial growth factor (VEGF) has been applied to the therapy of several neoplasms, but an appropriate biomarker to predict the efficacy has not been found. Tose markers can originate from peripheral circulation, tumor tissue and genes. Some resear...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000279/
https://www.ncbi.nlm.nih.gov/pubmed/21762631
http://dx.doi.org/10.3779/j.issn.1009-3419.2011.07.08
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collection PubMed
description Bevacizumab, the monoclonal antibody of vascular endothelial growth factor (VEGF) has been applied to the therapy of several neoplasms, but an appropriate biomarker to predict the efficacy has not been found. Tose markers can originate from peripheral circulation, tumor tissue and genes. Some researches have found that low level of vascular cell adhesion molecule-1 (VCAM-1), E-selectin, angiopoietin 2 (Ang-2) in circulation or carbonic anhydrase 9 (CA9), CD31- microvessel density (CD31-MVD) in tumor tissue can predict beter activity of bevacizumab. Moreover, high level of soluble VEGFR2 (sVEGFR2) in circulation or the ratio of phosphorylated-VEGFR2 (p-VEGFR2) and VEGFR2 in tumor tissue increasing has the same predictive function. As to the gene, VEGF-634 CC, VEGF-1498 T and VEGFR2 H472Q are only related to the side effct. Thus more clinical tirals and basic researches should be performed to fnd out effective biomarkers in bevacizumab's therapy.
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spelling pubmed-60002792018-07-06 预测贝伐珠单抗抗肿瘤治疗效果的生物学标记物 Zhongguo Fei Ai Za Zhi 综述 Bevacizumab, the monoclonal antibody of vascular endothelial growth factor (VEGF) has been applied to the therapy of several neoplasms, but an appropriate biomarker to predict the efficacy has not been found. Tose markers can originate from peripheral circulation, tumor tissue and genes. Some researches have found that low level of vascular cell adhesion molecule-1 (VCAM-1), E-selectin, angiopoietin 2 (Ang-2) in circulation or carbonic anhydrase 9 (CA9), CD31- microvessel density (CD31-MVD) in tumor tissue can predict beter activity of bevacizumab. Moreover, high level of soluble VEGFR2 (sVEGFR2) in circulation or the ratio of phosphorylated-VEGFR2 (p-VEGFR2) and VEGFR2 in tumor tissue increasing has the same predictive function. As to the gene, VEGF-634 CC, VEGF-1498 T and VEGFR2 H472Q are only related to the side effct. Thus more clinical tirals and basic researches should be performed to fnd out effective biomarkers in bevacizumab's therapy. 中国肺癌杂志编辑部 2011-07-20 /pmc/articles/PMC6000279/ /pubmed/21762631 http://dx.doi.org/10.3779/j.issn.1009-3419.2011.07.08 Text en 版权所有©《中国肺癌杂志》编辑部2017 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/
spellingShingle 综述
预测贝伐珠单抗抗肿瘤治疗效果的生物学标记物
title 预测贝伐珠单抗抗肿瘤治疗效果的生物学标记物
title_full 预测贝伐珠单抗抗肿瘤治疗效果的生物学标记物
title_fullStr 预测贝伐珠单抗抗肿瘤治疗效果的生物学标记物
title_full_unstemmed 预测贝伐珠单抗抗肿瘤治疗效果的生物学标记物
title_short 预测贝伐珠单抗抗肿瘤治疗效果的生物学标记物
title_sort 预测贝伐珠单抗抗肿瘤治疗效果的生物学标记物
topic 综述
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000279/
https://www.ncbi.nlm.nih.gov/pubmed/21762631
http://dx.doi.org/10.3779/j.issn.1009-3419.2011.07.08
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