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      Expression of P‐Glycoprotein mRNA in Human Gastric Tumors

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          Abstract

          We have isolated a cDNA clone, pCA12–2, from a 2 gt11 cDNA library of an adriamyciii‐resistant subline of human myelogenous leukemia K562 (K562/ADM) by plaque hybridization with the 2.6 kb genomic probe of P‐glycoprotein reported previously. The cDNA pCA12–2 was identified as the 3′‐part of P‐glycoprotein cDNA by dideoxy sequencing. By using the cDNA probe, expression of P‐glycoprotein mRNA was examined in human gastric xenograft lines transplanted in nude mice and clinical samples of human gastric normal tissues and tumors. Five gastric tumor xenograft lines expressed low but significant levels of P‐glycoprotein mRNA. The extent of expression was higher in some cases than that observed for R1–3, a weakly drug‐resistant subline of K562. Normal gastric tissues from three patients expressed similar levels of P‐glycoprotein mRNA and the extent of expression was slightly higher than that of R1–3. Two of three gastric tumor samples expressed higher levels of mRNA than normal gastric tissues. These results suggest that the intrinsic insensitivity of human gastric cancers to chemotherapy could be partly explained by the expression of P‐glycoprotein.

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          Most cited references42

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          A surface glycoprotein modulating drug permeability in Chinese hamster ovary cell mutants.

          Chinese hamster ovary cells selected for resistance to colchicine display pleiotropic cross-resistance to a wide range of amphiphilic drugs. The drug-resistant phenotype is due to a membrane alteration which reduces the rate of drug permeation. Surface labelling studies reveal that drug-resistant Chinese hamster ovary cell membranes possess a carbohydrate-containing component of 170 000 daltons apparent molecular weight which is not observed in wild type cells. Through studies of the metabolic incorporation of carbohydrate and protein precursors, and through the use of selective proteolysis, this component is shown to be a cell surface glycoprotein. Since this glycoprotein appears unique to mutant cells displaying altered drug permeability, we have designated it the P glycoprotein. The relative amount of surface labelled P glycoprotein correlates with the degree of drug resistance in a number of independent mutant and revertant clones. A similar high molecular weight glycoprotein is also present in drug-resistant mutants from another hamster cell line. Observations on the molecular basis of pleiotropic drug resistance are interpreted in terms of a model wherein certain surface glycoproteins control drug permeation by modulating the properties of hydrophobic membrane regions...
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            Internal duplication and homology with bacterial transport proteins in the mdr1 (P-glycoprotein) gene from multidrug-resistant human cells.

            Resistance of tumor cells to multiple cytotoxic drugs is a major impediment to cancer chemotherapy. Multidrug resistance in human cells is determined by the mdr1 gene, encoding a high molecular weight membrane glycoprotein (P-glycoprotein). Complete primary structure of human P-glycoprotein has been determined from the cDNA sequence. The protein, 1280 amino acids long, consists of two homologous parts of approximately equal length. Each half of the protein includes a hydrophobic region with six predicted transmembrane segments and a hydrophilic region. The hydrophilic regions share homology with peripheral membrane components of bacterial active transport systems and include potential nucleotide-binding sites. These results are consistent with a function for P-glycoprotein as an energy-dependent efflux pump responsible for decreased drug accumulation in multidrug-resistant cells.
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              A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.

              A technique for conveniently radiolabeling DNA restriction endonuclease fragments to high specific activity is described. DNA fragments are purified from agarose gels directly by ethanol precipitation and are then denatured and labeled with the large fragment of DNA polymerase I, using random oligonucleotides as primers. Over 70% of the precursor triphosphate is routinely incorporated into complementary DNA, and specific activities of over 10(9) dpm/microgram of DNA can be obtained using relatively small amounts of precursor. These "oligolabeled" DNA fragments serve as efficient probes in filter hybridization experiments.
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                Author and article information

                Journal
                Jpn J Cancer Res
                Jpn. J. Cancer Res
                10.1111/(ISSN)1349-7006a
                CAS
                Japanese Journal of Cancer Research : Gann
                Blackwell Publishing Ltd (Oxford, UK )
                0910-5050
                1876-4673
                October 1989
                : 80
                : 10 ( doiID: 10.1111/cas.1989.80.issue-10 )
                : 993-999
                Affiliations
                [ 1 ]Cancer Chemotherapy Center, Japanese Foundation for Cancer Research, Kami‐Ikebukuro, Toshima‐ku, Tokyo 170
                [ 2 ]Institute of Applied Microbiology, University of Tokyo, Yayoi, Bunkyo‐ku, Tokyo 113
                Author notes
                [*] [* ]To whom correspondence and requests for reprints should be addressed.
                Article
                CAE993
                10.1111/j.1349-7006.1989.tb01639.x
                5917879
                2575610
                5e42e098-cd63-479a-95d4-a7acad23ac49
                History
                Page count
                References: 46, Pages: 7
                Categories
                Article
                Custom metadata
                2.0
                October 1989
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.6.9 mode:remove_FC converted:04.11.2015

                multidrug resistance,p‐glycoprotein,human gastric tumor,cancer chemotherapy

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