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Verfasst von:Grottke, Claudia [VerfasserIn]   i
 Schadendorf, Dirk [VerfasserIn]   i
Titel:Identification of differentially expressed genes in human melanoma cells with acquired resistance to various antineoplastic drugs
Verf.angabe:Claudia Grottke, Klaus Mantwill, Manfred Dietel, Dirk Schadendorf and Hermann Lage
Umfang:12 S.
Fussnoten:Gesehen am 01.03.2019
Titel Quelle:Enthalten in: International journal of cancer
Jahr Quelle:2000
Band/Heft Quelle:88(2000), 4, S. 535-546
ISSN Quelle:1097-0215
Abstract:Malignant melanoma displays strong resistance against various antineoplastic drugs. The mechanisms conferring this intrinsic resistance are unclear. To better understand the molecular events associated with drug resistance in melanoma, a panel of human melanoma cell variants exhibiting low and high levels of resistance to 4 commonly used drugs in melanoma treatment, i.e., vindesine, etoposide, fotemustine and cisplatin, was characterized by differential display reverse transcription-polymerase chain reaction (DDRT-PCR). Of 269 mRNA fragments found to be altered in expression level by DDRT-PCR, a total of 11 cDNA clones was characterized after confirmation of a differential expression pattern by Northern blot analyses. These clones include 3 genes (DSM-1, DSM-3 and DSM-5) of known function, 4 previously sequenced genes (DSM-2, DSM-4, DSM-6 and DSM-7) of uncharacterized function and 4 novel genes (DSM-8-DSM-11) without match in GenBank. All of these genes exhibited altered mRNAexpression in high level etoposide-resistant cells, whereby 7 genes (DSM-1-DSM-6 and DSM-8) were found to be decreased in the transcription rate in these etoposide-resistant cells. The mRNA synthesis of the remaining genes (DSM-7 and DSM-9-DSM11) was enhanced in high level etoposide-resistant melanoma cells. The expression of 5 (DSM-5 and DSM-7-DSM-10) of the cloned cDNA encoding mRNAs was modulated in various independently established drug-resistant melanoma cells, indicating to be associated with drug resistance. Further characterization of these genes may yield inside into the biology and development of drug resistance in malignant melanoma.
DOI:doi:10.1002/1097-0215(20001115)88:4<535¬AID-IJC4>3.0.CO;2-V
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Verlag: http://dx.doi.org/10.1002/1097-0215(20001115)88:4<535AID-IJC4>3.0.CO;2-V
 Verlag: https://onlinelibrary.wiley.com/doi/abs/10.1002/1097-0215%2820001115%2988%3A4%3C535%3A%3AAID-IJC4%3E3.0.CO%3B2-V
 DOI: https://doi.org/10.1002/1097-0215(20001115)88:4<535AID-IJC4>3.0.CO;2-V
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1588258017
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