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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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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. |
format | Online Article Text |
id | pubmed-4749816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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