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PMID: 3468517 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Cross-resistance patterns and antigen expression in Vinca alkaloid- and other multiple drug-resistant human leukemic cell lines.

Progress in clinical and biological research ·Vol. 223 ·1986-00-00 ·Pages 3-10

Beck WT, Danks MK, Cirtain MC, van Heiningen JN

Abstract

The studies presented in this report demonstrate that Vinca alkaloid-resistant human leukemic lymphoblasts display patterns of cross-resistance to other drugs that differ from those of cell lines selected for primary resistance to anthracyclines or epipodophyllotoxins. These various drug-resistant cell lines also showed differential expression of an antigen recognized by an antibody that distinguishes VLB-resistant from VLB-sensitive cells. Furthermore, comparable levels of resistance or cross-resistance to one drug are not predictive of cross-resistance to other drugs. Our data suggest, then, that the MDR phenotype is complex and may be the result of many and different biochemical lesions. Thus, in order to predict MDR, it may be necessary to document more than one of these changes with specific reagents.

MeSH Terms
Antibodies, Monoclonal/immunology Antigens, Neoplasm/analysis Antigens, Surface/analysis Antimetabolites, Antineoplastic/pharmacology Cell Line Drug Resistance Flow Cytometry Humans Leukemia, Lymphoid/drug therapy Vinca Alkaloids/pharmacology
Chemicals
Antibodies, Monoclonal Antigens, Neoplasm Antigens, Surface Antimetabolites, Antineoplastic Vinca Alkaloids
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Beck W T
Danks M K
Cirtain M C
van Heiningen J N
Article Info
Journal
Progress in clinical and biological research
Abbr.
Prog Clin Biol Res
ISSN
0361-7742
Published
1986-00-00
Pages
3-10
Language
English
Region
United States
NLM ID
7605701
Subset
IM
Grants
NCI NIH HHS · CA 06795 · United States
NCI NIH HHS · CA 21765 · United States
NCI NIH HHS · CA 30103 · United States
External Links
PubMed source
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