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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004260naa a2200481 4500
001oai:DiVA.org:liu-98827
003SwePub
008131014s1999 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:1944032
024a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-988272 URI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:19440322 URI
024a https://doi.org/10.1016/S0891-5849(99)00101-X2 DOI
040 a (SwePub)liud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Sasada, T.u Department of Biological Responses, Institute for Virus Research, Kyoto University, Kyoto, Japan4 aut
2451 0a Possible involvement of thioredoxin reductase as well as thioredoxin in cellular sensitivity to cis-diamminedichloroplatinum (II)
264 1b Elsevier,c 1999
338 a print2 rdacarrier
520 a The thioredoxin (TRX) system, composed of nicotinamide adenine dinucleotide phosphate (reduced form), TRX, and TRX reductase (TRXR), has multiple biologic functions via thiol-mediated redox control. In this study, we investigated the relationship between intracellular TRXR levels and cellular sensitivity to cis-diamminedichloroplatinum (II) (CDDP). HeLa, a human cervical carcinoma cell line, cultured with CDDP showed a time- and dose-dependent reduction of intracellular TRXR activity, which was well correlated with the decrease in cell viability after exposure to CDDP. In a cell-free system, CDDP was found to directly inactivate the reduced form of purified human TRXR. The CDDP-resistant variants of HeLa cells, established by continuous exposure to CDDP, exhibited an increased expression and activity of TRXR as well as TRX compared with the parental cells. In addition, sodium selenate, an inhibitor of TRXR, was found to increase the susceptibility to CDDP in the CDDP-resistant cells. Moreover, the HeLa cells transfected with an antisense TRXR RNA expression vector to reduce the intracellular enzyme activity displayed an enhanced sensitivity to CDDP. Taken together with previous reports on TRX, these results indicate the possible involvement of TRXR as well as TRX in the cellular sensitivity and resistance to CDDP.
653 a Thioredoxin
653 a Thioredoxin reductase
653 a cis-Diamminedichloroplatinum (II)
653 a Cytotoxicity
653 a Redox
653 a Free radicals
700a Nakamura, H.u Department of Biological Responses, Institute for Virus Research, Kyoto University, Kyoto, Japan4 aut
700a Ueda, S.u Department of Biological Responses, Institute for Virus Research, Kyoto University, Kyoto, Japan4 aut
700a Sato, N.u Department of Biological Responses, Institute for Virus Research, Kyoto University, Kyoto, Japan4 aut
700a Kitaoka, Y.u Department of Biological Responses, Institute for Virus Research, Kyoto University, Kyoto, Japan4 aut
700a Gon, Y.u Department of Biological Responses, Institute for Virus Research, Kyoto University, Kyoto, Japan4 aut
700a Takabayashi, A.u Department of Surgery, Tazuke Kofukai Kitano Hospital Medical Institute, Osaka, Japan4 aut
700a Spyrou, Giannisu Medical Nobel Institute for Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden4 aut0 (Swepub:liu)ioasp42
700a Holmgren, Arneu Karolinska Institutet4 aut
700a Yodoi, J.u Department of Biological Responses, Institute for Virus Research, Kyoto University, Kyoto, Japan4 aut
710a Department of Biological Responses, Institute for Virus Research, Kyoto University, Kyoto, Japanb Department of Surgery, Tazuke Kofukai Kitano Hospital Medical Institute, Osaka, Japan4 org
773t Free Radical Biology & Medicined : Elsevierg 27:5-6, s. 504-514q 27:5-6<504-514x 0891-5849x 1873-4596
856u http://www.sciencedirect.com/science/article/pii/S089158499900101X#y Link to article
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-98827
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:1944032
8564 8u https://doi.org/10.1016/S0891-5849(99)00101-X

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