dc.contributor.author |
Sun, JD |
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dc.contributor.author |
Liu, Q |
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dc.contributor.author |
Wang, J |
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dc.contributor.author |
Ahluwalia, D |
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dc.contributor.author |
Ferraro, D |
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dc.contributor.author |
Wang, Y |
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dc.contributor.author |
Duan, JX |
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dc.contributor.author |
Ammons, WS |
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dc.contributor.author |
Curd, JG |
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dc.contributor.author |
Matteucci, MD |
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dc.contributor.author |
Hart, CP |
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dc.coverage.spatial |
United States |
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dc.date.accessioned |
2012-06-12T23:19:13Z |
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dc.date.available |
2012-06-12T23:19:13Z |
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dc.date.issued |
2012 |
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dc.identifier.citation |
Clin Cancer Res 18(3):758-770 01 Feb 2012 |
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dc.identifier.issn |
1078-0432 |
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dc.identifier.other |
1078-0432.CCR-11-1980 |
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dc.identifier.uri |
http://hdl.handle.net/2292/18965 |
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dc.description.abstract |
Tumor hypoxia underlies treatment failure and yields a more aggressive, invasive, and metastatic cancer phenotype. TH-302 is a 2-nitroimidazole triggered hypoxia-activated prodrug of the cytotoxin bromo-isophosphoramide mustard (Br-IPM). The purpose of this study is to characterize the antitumor activity of TH-302 and investigate its selective targeting of the hypoxic cells in human tumor xenograft models. |
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dc.language |
eng |
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dc.publisher |
American Association for Cancer Research |
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dc.relation.ispartofseries |
Clinical Cancer Research |
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dc.rights |
Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. |
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dc.rights.uri |
https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm |
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dc.source.uri |
http://dx.doi.org/10.1158/1078-0432.CCR-11-1980 |
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dc.subject |
Animals |
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dc.subject |
Antineoplastic Agents |
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dc.subject |
Cell Hypoxia |
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dc.subject |
Cell Line, Tumor |
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dc.subject |
Female |
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dc.subject |
Humans |
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dc.subject |
Immunohistochemistry |
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dc.subject |
Mice |
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dc.subject |
Mice, SCID |
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dc.subject |
Neoplasms, Experimental |
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dc.subject |
Neovascularization, Pathologic |
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dc.subject |
Nitroimidazoles |
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dc.subject |
Phosphoramide Mustards |
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dc.subject |
Prodrugs |
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dc.subject |
Xenograft Model Antitumor Assays |
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dc.title |
Selective tumor hypoxia targeting by hypoxia-activated prodrug TH-302 inhibits tumor growth in preclinical models of cancer. |
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dc.type |
Journal Article |
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dc.identifier.doi |
10.1158/1078-0432.CCR-11-1980 |
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pubs.issue |
3 |
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pubs.begin-page |
758 |
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pubs.volume |
18 |
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dc.rights.holder |
Copyright: American Association for Cancer Research |
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pubs.end-page |
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dc.rights.accessrights |
http://purl.org/eprint/accessRights/RestrictedAccess |
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pubs.elements-id |
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