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Immunotoxin therapy of cancer
Abstract
Rationally designed anticancer agents that target cell-surface antigens or receptors represent a promising approach for treating cancer patients. However, antibodies that bind these targets are often, by themselves, non-cytotoxic. By attaching potent toxins we can dramatically improve the clinical utility of some anti-tumour antibodies. Here we describe the construction and clinical utility of several recombinant immunotoxins; each of which is composed of antibody Fv fragments fused to powerful bacterial toxins. Results from clinical trials indicate that recombinant immunotoxins and similar agents that are designed to combine antibody selectivity with toxin cell-killing potency will be useful additions to cancer therapy.
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Cited by
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Strebhardt, K., & Ullrich, A. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2394 · Cited by 1,457
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Thomas, A., Teicher, B. A., & Hassan, R. (2016) · The Lancet Oncology · doi:10.1016/s1470-2045(16)30030-4 · Cited by 606
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Hassan, R., & Ho, M. (2008) · European Journal of Cancer · doi:10.1016/j.ejca.2007.08.028 · Cited by 340
Self-citationAutophagy regulates selective HMGB1 release in tumor cells that are destined to die
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Metadata
- Authors
- Pastan, I., Hassan, R., FitzGerald, D. J., & Kreitman, R. J.
- Venue
- Nature Reviews Cancer
- Published
- 2006-07
- Volume
- 6
- Issue
- 7
- Pages
- 559-565
- ISSN
- 1474-175X (ISSN-L)
- 1474-1768
- OpenAlex
- W2009013652
- Cited by
- 528
- References
- 0
- FWCI
- 1.64
- Type
- journal article
- Language
- en
- Open access
- closed
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