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Circulating Carbonic Anhydrase IX and Antiangiogenic Therapy in Breast Cancer

Introduction. Carbonic anhydrase IX (CAIX) is a hypoxia regulated metalloenzyme integral to maintaining cellular pH. Increased CAIX expression is associated with poor prognosis in breast cancer. To explore CAIX as a biomarker for breast cancer therapies, we measured plasma CAIX levels in healthy con...

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Autores principales: Brown-Glaberman, Ursa, Marron, Marilyn, Chalasani, Pavani, Livingston, Robert, Iannone, Maria, Specht, Jennifer, Stopeck, Alison T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749816/
https://www.ncbi.nlm.nih.gov/pubmed/26941473
http://dx.doi.org/10.1155/2016/9810383
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author Brown-Glaberman, Ursa
Marron, Marilyn
Chalasani, Pavani
Livingston, Robert
Iannone, Maria
Specht, Jennifer
Stopeck, Alison T.
author_facet Brown-Glaberman, Ursa
Marron, Marilyn
Chalasani, Pavani
Livingston, Robert
Iannone, Maria
Specht, Jennifer
Stopeck, Alison T.
author_sort Brown-Glaberman, Ursa
collection PubMed
description Introduction. Carbonic anhydrase IX (CAIX) is a hypoxia regulated metalloenzyme integral to maintaining cellular pH. Increased CAIX expression is associated with poor prognosis in breast cancer. To explore CAIX as a biomarker for breast cancer therapies, we measured plasma CAIX levels in healthy control subjects and in breast cancer patients. Methods. In control subjects we evaluated plasma CAIX stability via commercially available ELISA. We then similarly quantified plasma CAIX levels in (1) locally advanced breast cancer (LABC) patients treated with neoadjuvant paclitaxel + sunitinib (T + S) followed by doxorubicin and cyclophosphamide (AC); (2) metastatic breast cancer (MBC) patients treated with systemic chemotherapy. Results. Plasma CAIX levels were stable at room temperature for at least 48 hours in control subjects. Mean baseline plasma CAIX levels were lower in controls compared to patients with LABC or MBC. In LABC, CAIX levels rose significantly in response to administration of antiangiogenic therapy (T + S) (p = 0.02) but not AC (p = 0.37). In patients with MBC treated without an antiangiogenic agent CAIX levels did not change with therapy. Conclusions. Our results suggest that CAIX may be an easily obtained, stable measure of tumor associated hypoxia as well as a useful pharmacodynamic biomarker for antiangiogenic therapy.
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spelling pubmed-47498162016-03-03 Circulating Carbonic Anhydrase IX and Antiangiogenic Therapy in Breast Cancer Brown-Glaberman, Ursa Marron, Marilyn Chalasani, Pavani Livingston, Robert Iannone, Maria Specht, Jennifer Stopeck, Alison T. Dis Markers Research Article Introduction. Carbonic anhydrase IX (CAIX) is a hypoxia regulated metalloenzyme integral to maintaining cellular pH. Increased CAIX expression is associated with poor prognosis in breast cancer. To explore CAIX as a biomarker for breast cancer therapies, we measured plasma CAIX levels in healthy control subjects and in breast cancer patients. Methods. In control subjects we evaluated plasma CAIX stability via commercially available ELISA. We then similarly quantified plasma CAIX levels in (1) locally advanced breast cancer (LABC) patients treated with neoadjuvant paclitaxel + sunitinib (T + S) followed by doxorubicin and cyclophosphamide (AC); (2) metastatic breast cancer (MBC) patients treated with systemic chemotherapy. Results. Plasma CAIX levels were stable at room temperature for at least 48 hours in control subjects. Mean baseline plasma CAIX levels were lower in controls compared to patients with LABC or MBC. In LABC, CAIX levels rose significantly in response to administration of antiangiogenic therapy (T + S) (p = 0.02) but not AC (p = 0.37). In patients with MBC treated without an antiangiogenic agent CAIX levels did not change with therapy. Conclusions. Our results suggest that CAIX may be an easily obtained, stable measure of tumor associated hypoxia as well as a useful pharmacodynamic biomarker for antiangiogenic therapy. Hindawi Publishing Corporation 2016 2016-01-28 /pmc/articles/PMC4749816/ /pubmed/26941473 http://dx.doi.org/10.1155/2016/9810383 Text en Copyright © 2016 Ursa Brown-Glaberman et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Brown-Glaberman, Ursa
Marron, Marilyn
Chalasani, Pavani
Livingston, Robert
Iannone, Maria
Specht, Jennifer
Stopeck, Alison T.
Circulating Carbonic Anhydrase IX and Antiangiogenic Therapy in Breast Cancer
title Circulating Carbonic Anhydrase IX and Antiangiogenic Therapy in Breast Cancer
title_full Circulating Carbonic Anhydrase IX and Antiangiogenic Therapy in Breast Cancer
title_fullStr Circulating Carbonic Anhydrase IX and Antiangiogenic Therapy in Breast Cancer
title_full_unstemmed Circulating Carbonic Anhydrase IX and Antiangiogenic Therapy in Breast Cancer
title_short Circulating Carbonic Anhydrase IX and Antiangiogenic Therapy in Breast Cancer
title_sort circulating carbonic anhydrase ix and antiangiogenic therapy in breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749816/
https://www.ncbi.nlm.nih.gov/pubmed/26941473
http://dx.doi.org/10.1155/2016/9810383
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