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PMID: 9461199 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

bcl-2 antisense therapy chemosensitizes human melanoma in SCID mice.

Nature medicine ·Vol. 4 ·No. 2 ·1998-02-00 ·Pages 232-4

Jansen B, Schlagbauer-Wadl H, Brown BD, Bryan RN, van Elsas A, Müller M, Wolff K, Eichler HG, Pehamberger H

Abstract

Malignant melanoma is a prime example of cancers that respond poorly to various treatment modalities including chemotherapy. A number of chemotherapeutic agents have been shown recently to act by inducing apoptosis, a type of cell death antagonized by the bcl-2 gene. Human melanoma expresses Bcl-2 in up to 90% of all cases. In the present study we demonstrate that bcl-2 antisense oligonucleotide treatment improves the chemosensitivity of human melanoma grown in severe combined immunodeficient (SCID) mice. Our findings suggest that reduction of Bcl-2 in melanoma, and possibly also in a variety of other tumors, may be a novel and rational approach to improve chemosensitivity and treatment outcome.

MeSH Terms
Actins/drug effects,metabolism Animals Antineoplastic Agents/pharmacology Apoptosis/drug effects,genetics Dacarbazine/pharmacology Female Humans Melanoma/drug therapy,genetics Mice Mice, SCID Neoplasm Transplantation Oligonucleotides, Antisense/pharmacology Proto-Oncogene Proteins c-bcl-2/drug effects,genetics,metabolism Transplantation, Heterologous
Chemicals
Actins Antineoplastic Agents Oligonucleotides, Antisense Proto-Oncogene Proteins c-bcl-2 Dacarbazine
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Jansen B
Department of Clinical Pharmacology, University of Vienna, Austria.
Schlagbauer-Wadl H
Brown B D
Bryan R N
van Elsas A
Müller M
Wolff K
Eichler H G
Pehamberger H
Article Info
Journal
Nature medicine
Abbr.
Nat Med
ISSN
1078-8956
Published
1998-02-00
Pages
232-4
Language
English
Region
United States
NLM ID
9502015
Subset
IM
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