Retrovirus–mediated wild–type P53 gene transfer to tumors of patients with lung cancer. View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1996-09

AUTHORS

J.A. Roth, D. Nguyen, D.D. Lawrence, B.L. Kemp, C.H. Carrasco, D.Z. Ferson, W.K. Hong, R. Komaki, J.J. Lee, J.C. Nesbitt, K.M.W. Pisters, J.B. Putnam, R. Schea, D.M. Shin, G.L. Walsh, M.M. Dolormente, C.-I. Han, F.D. Martin, N. Yen, K. Xu, L.C. Stephens, T.J. Mcdonnell, T. Mukhopadhyay, D. Cai

ABSTRACT

A retroviral vector containing the wild–type p53 gene under control of a β–actin promoter was produced to mediate transfer of wild–type p53 into human non–small cell lung cancers by direct injection. Nine patients whose conventional treatments failed were entered into the study. No clinically significant vector–related toxic effects were noted up to five months after treatment. In situ hybridization and DNA polymerase chain reaction showed vector–p53 sequences in posttreatment biopsies. Apoptosis (programmed cell death) was more frequent in posttreatment biopsies than in pretreatment biopsies. Tumor regression was noted in three patients, and tumor growth stabilized in three other patients. More... »

PAGES

985-991

Journal

TITLE

Nature Medicine

ISSUE

9

VOLUME

2

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/nm0996-985

DOI

http://dx.doi.org/10.1038/nm0996-985

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1019494129

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/8782455


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346 Department of Veterinary Medicine and Surgery, The University of Texas M.D. Anderson Cancer Center, 77030, Houston, Texas, USA
347 Section of Thoracic Molecular Oncology, Department of Thoracic and Cardiovascular Surgery, The University of Texas M.D. Anderson Cancer Center, 77030, Houston, Texas, USA
348 rdf:type schema:Organization
 




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