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PMID: 9407950 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

The 95-kilodalton membrane glycoprotein overexpressed in novel multidrug-resistant breast cancer cells is NCA, the nonspecific cross-reacting antigen of carcinoembryonic antigen.

Cancer research ·Vol. 57 ·No. 24 ·1997-12-15 ·Pages 5460-4

Ross DD, Gao Y, Yang W, Leszyk J, Shively J, Doyle LA

Abstract

Human breast carcinoma MCF-7/AdrVp cells display a novel multidrug resistance phenotype that is characterized by the overexpression of a 95-kDa membrane glycoprotein (p95) and by marked reduction in intracellular anthracycline accumulation, without overexpression of P-glycoprotein or the multidrug resistance protein MRP. p95 is also highly expressed in multidrug-resistant NCI-H1688 cells derived from a human small cell lung carcinoma. Deglycoslyated p95 from NCI-H1688 cells was isolated by two-dimensional gel electrophoresis and then digested with trypsin. The tryptic peptides were analyzed by mass spectrometry and microsequencing. These analyses identified p95 to be identical to NCA-90, the nonspecific cross-reacting antigen related to the carcinoembryonic antigen (CEA). Further confirmation that p95 is indeed NCA-90 was obtained by Northern and Western blot studies using probes or antibodies specific for p95, NCA-90, or CEA family members. Western blot studies also revealed that CEA itself is overexpressed in MCF-7/AdrVp cells compared to parental MCF-7/W cells. The enforced expression of NCA-90 protein in HeLa cells stably transfected with NCA-90 cDNA did not result in increased resistance of the transfected cells to daunorubicin or a decrease in daunorubicin accumulation in the transfected cells compared to cells transfected only with the expression vector. However, a recent report by H. Kawaharata et al. (Int. J. Cancer, 72: 377-382, 1997) of diminished accumulation, retention, and cytotoxicity of doxorubicin in EJNIH3T3 cells in which enforced expression of CEA was accomplished leaves open the possibility that the overexpression of CEA, possibly in combination with that of NCA-90, could account at least in part for the drug resistant phenotype displayed by MCF-7/AdrVp cells.

MeSH Terms
3T3 Cells/metabolism Amino Acid Sequence Animals Antibiotics, Antineoplastic/pharmacology Antigens, Neoplasm Blotting, Western Breast Neoplasms/chemistry,drug therapy,metabolism Carcinoembryonic Antigen/immunology Cell Adhesion Molecules Cross Reactions Doxorubicin/pharmacology Drug Resistance, Multiple Drug Resistance, Neoplasm Electrophoresis, Gel, Two-Dimensional Epitopes HeLa Cells Humans Isoelectric Focusing Membrane Glycoproteins/biosynthesis,chemistry,isolation & purification Mice Molecular Sequence Data Neoplasm Proteins/biosynthesis,chemistry,isolation & purification Phenotype Sodium Dodecyl Sulfate Tumor Cells, Cultured
Chemicals
Antibiotics, Antineoplastic Antigens, Neoplasm Carcinoembryonic Antigen Cell Adhesion Molecules Epitopes Membrane Glycoproteins Neoplasm Proteins Sodium Dodecyl Sulfate Doxorubicin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Ross D D
Greenebaum Cancer Center of the University of Maryland and the Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA. dross@umcc01.umcc.ab.umd.edu
Gao Y
Yang W
Leszyk J
Shively J
Doyle L A
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1997-12-15
Pages
5460-4
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
NCI NIH HHS · R01 CA52178 · United States
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