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Article has an altmetric score of 9

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Referenced in 7 patents
22 readers on Mendeley
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Research Article Free access | 10.1172/JCI118370

Targeted tumor killing via an intracellular antibody against erbB-2.

J Deshane, G P Siegal, R D Alvarez, M H Wang, M Feng, G Cabrera, T Liu, M Kay, and D T Curiel

Gene Therapy Program, University of Alabama at Birmingham, 35294, USA.

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Gene Therapy Program, University of Alabama at Birmingham, 35294, USA.

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Gene Therapy Program, University of Alabama at Birmingham, 35294, USA.

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Gene Therapy Program, University of Alabama at Birmingham, 35294, USA.

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Gene Therapy Program, University of Alabama at Birmingham, 35294, USA.

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Gene Therapy Program, University of Alabama at Birmingham, 35294, USA.

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Gene Therapy Program, University of Alabama at Birmingham, 35294, USA.

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Gene Therapy Program, University of Alabama at Birmingham, 35294, USA.

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Gene Therapy Program, University of Alabama at Birmingham, 35294, USA.

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Published December 1, 1995 - More info

Published in Volume 96, Issue 6 on December 1, 1995
J Clin Invest. 1995;96(6):2980–2989. https://doi.org/10.1172/JCI118370.
© 1995 The American Society for Clinical Investigation
Published December 1, 1995 - Version history
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Abstract

Specific killing of erbB-2-overexpressing tumor cells can be achieved using expression of an intracellular antibody directed against the erbB-2 oncoprotein. We have developed a strategy using a recombinant adenovirus encoding an anti-erbB-2 single chain antibody to achieve targeted tumor cell killing in vivo and can show significantly prolonged survival of animals carrying a human ovarian carcinoma tumor burden within their peritoneal cavities. This strategy of gene therapy for ovarian carcinoma offers the potential to achieve highly specific, targeted killing of human tumor cells and thus establishes the rationale to undertake human clinical trials on this basis.

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Referenced in 7 patents
22 readers on Mendeley
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