IOVS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Originally published In Press as doi:10.1167/iovs.08-1751 on March 7, 2008
(Investigative Ophthalmology and Visual Science. 2008;49:2799-2805.)
© 2008 by The Association for Research in Vision and Ophthalmology, Inc.
doi:10.1167/iovs.08-1751

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
iovs.08-1751v1
49/7/2799    most recent
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (3)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Boutrid, H.
Right arrow Articles by Cebulla, C. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Boutrid, H.
Right arrow Articles by Cebulla, C. M.

Targeting Hypoxia, a Novel Treatment for Advanced Retinoblastoma

Hinda Boutrid,1 Maria-Elena Jockovich,1 Timothy G. Murray,1 Yolanda Piña,1 William J. Feuer,1 Theodore J. Lampidis,2 and Colleen M. Cebulla1

1From the Bascom Palmer Eye Institute, Department of Ophthalmology, University of Miami Miller School of Medicine, Miami, Florida; and the 2Department of Cell Biology and Anatomy, University of Miami Miller School of Medicine and Sylvester Comprehensive Cancer Center, Miami, Florida.

PURPOSE. The purpose of this study was to evaluate the presence and extent of hypoxia in murine retinoblastoma tumors and the feasibility of targeting hypoxic cells as a novel therapeutic strategy.

METHODS. Hypoxic and vascular areas in LHBETATAG mouse retinal tumors were measured using immunohistochemistry. The glycolytic inhibitor 2-deoxy-D-glucose (2-DG) was used to test the efficacy of targeting hypoxic cells in retinoblastoma. Sixteen-week-old LHBETATAG mice received injections of saline, carboplatin (31.25 µg/20 µL), 2-DG (500 mg/kg), and carboplatin (31.25 µg/20 µL) + 2-DG (500 mg/kg). Carboplatin was administered through biweekly subconjunctival injections to right eyes only for 3 weeks. 2-DG was administered through intraperitoneal injection three times a week for 5 weeks. Saline was administered using both methods. Eyes were enucleated at 21 weeks of age and examined for residual tumor.

RESULTS. Hypoxic regions were observed in tumors larger than 3.28 mm2. When 2-DG was combined with carboplatin, a marked decrease in tumor burden was observed that was significantly more pronounced than when either agent was given alone. The hypoxic tumor cell population as measured by pimonidazole was markedly reduced by carboplatin + 2-DG (P < 0.01) and by 2-DG alone (P < 0.01), but not by carboplatin alone, indicating that 2-DG effectively killed hypoxic retinoblastoma cells in vivo.

CONCLUSIONS. Treatment with glycolytic inhibitors as adjuvants to chemotherapy has the potential to increase the efficacy of chemotherapy in advanced retinoblastoma. This approach may have benefits for children with this disease and should be further investigated.





This article has been cited by other articles:


Home page
IOVSHome page
H. Boutrid, Y. Pina, C. M. Cebulla, W. J. Feuer, T. J. Lampidis, M.-E. Jockovich, and T. G. Murray
Increased Hypoxia following Vessel Targeting in a Murine Model of Retinoblastoma
Invest. Ophthalmol. Vis. Sci., December 1, 2009; 50(12): 5537 - 5543.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2008 by the Association for Research in Vision and Ophthalmology