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Glycoprotein non-metastatic b (GPNMB): A metastatic mediator and emerging therapeutic target in cancer

Molecularly targeted therapies are rapidly growing with respect to their clinical development and impact on cancer treatment due to their highly selective anti-tumor action. However, many aggressive cancers such as triple-negative breast cancer (TNBC) currently lack well-defined therapeutic targets...

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Detalles Bibliográficos
Autores principales: Maric, Gordana, Rose, April AN, Annis, Matthew G, Siegel, Peter M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3711880/
https://www.ncbi.nlm.nih.gov/pubmed/23874106
http://dx.doi.org/10.2147/OTT.S44906
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author Maric, Gordana
Rose, April AN
Annis, Matthew G
Siegel, Peter M
author_facet Maric, Gordana
Rose, April AN
Annis, Matthew G
Siegel, Peter M
author_sort Maric, Gordana
collection PubMed
description Molecularly targeted therapies are rapidly growing with respect to their clinical development and impact on cancer treatment due to their highly selective anti-tumor action. However, many aggressive cancers such as triple-negative breast cancer (TNBC) currently lack well-defined therapeutic targets against which such agents can be developed. The identification of tumor-associated antigens and the generation of antibody drug-conjugates represent an emerging area of intense interest and growth in the field of cancer therapeutics. Glycoprotein non-metastatic b (GPNMB) has recently been identified as a gene that is over-expressed in numerous cancers, including TNBC, and often correlates with the metastatic phenotype. In breast cancer, GPNMB expression in the tumor epithelium is associated with a reduction in disease-free and overall survival. Based on these findings, glembatumumab vedotin (CDX-011), an antibody-drug conjugate that selectively targets GPNMB, is currently being investigated in clinical trials for patients with metastatic breast cancer and unresectable melanoma. This review discusses the physiological and potential pathological roles of GPNMB in normal and cancer tissues, respectively, and details the clinical advances and challenges in targeting GPNMB-expressing malignancies.
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spelling pubmed-37118802013-07-19 Glycoprotein non-metastatic b (GPNMB): A metastatic mediator and emerging therapeutic target in cancer Maric, Gordana Rose, April AN Annis, Matthew G Siegel, Peter M Onco Targets Ther Review Molecularly targeted therapies are rapidly growing with respect to their clinical development and impact on cancer treatment due to their highly selective anti-tumor action. However, many aggressive cancers such as triple-negative breast cancer (TNBC) currently lack well-defined therapeutic targets against which such agents can be developed. The identification of tumor-associated antigens and the generation of antibody drug-conjugates represent an emerging area of intense interest and growth in the field of cancer therapeutics. Glycoprotein non-metastatic b (GPNMB) has recently been identified as a gene that is over-expressed in numerous cancers, including TNBC, and often correlates with the metastatic phenotype. In breast cancer, GPNMB expression in the tumor epithelium is associated with a reduction in disease-free and overall survival. Based on these findings, glembatumumab vedotin (CDX-011), an antibody-drug conjugate that selectively targets GPNMB, is currently being investigated in clinical trials for patients with metastatic breast cancer and unresectable melanoma. This review discusses the physiological and potential pathological roles of GPNMB in normal and cancer tissues, respectively, and details the clinical advances and challenges in targeting GPNMB-expressing malignancies. Dove Medical Press 2013-07-09 /pmc/articles/PMC3711880/ /pubmed/23874106 http://dx.doi.org/10.2147/OTT.S44906 Text en © 2013 Maric et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Maric, Gordana
Rose, April AN
Annis, Matthew G
Siegel, Peter M
Glycoprotein non-metastatic b (GPNMB): A metastatic mediator and emerging therapeutic target in cancer
title Glycoprotein non-metastatic b (GPNMB): A metastatic mediator and emerging therapeutic target in cancer
title_full Glycoprotein non-metastatic b (GPNMB): A metastatic mediator and emerging therapeutic target in cancer
title_fullStr Glycoprotein non-metastatic b (GPNMB): A metastatic mediator and emerging therapeutic target in cancer
title_full_unstemmed Glycoprotein non-metastatic b (GPNMB): A metastatic mediator and emerging therapeutic target in cancer
title_short Glycoprotein non-metastatic b (GPNMB): A metastatic mediator and emerging therapeutic target in cancer
title_sort glycoprotein non-metastatic b (gpnmb): a metastatic mediator and emerging therapeutic target in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3711880/
https://www.ncbi.nlm.nih.gov/pubmed/23874106
http://dx.doi.org/10.2147/OTT.S44906
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