Association of genomic imbalances with drug resistance and thermoresistance in human gastric carcinoma cells

被引:13
作者
Tönnies, H
Poland, J
Sinha, P
Lage, H
机构
[1] Humboldt Univ, Inst Pathol, D-10117 Berlin, Germany
[2] Humboldt Univ, Inst Human Genet, D-10117 Berlin, Germany
[3] Humboldt Univ, Inst Lab Med & Pathobiochem, D-10117 Berlin, Germany
关键词
drug resistance; thermoresistance; gastric carcinoma; EPG85-257;
D O I
10.1002/ijc.10905
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Therapy resistance is the major obstacle to advances in successful cancer treatment. To characterize chromosomal alterations associated with different types of acquired MDR and thermoresistance, we applied CGH to compare a unique panel of human gastric carcinoma cells consisting of the parental, drug-sensitive and thermosensitive cancer cell line EPG85-257P, the atypical MDR variant EPG85-257RNOV, the classical MDR subline EPG85-257RDB and their thermoresistant counterparts EPG85-257P-TR, EPG85-257RNOV-TR and EPG85-257RDB-TR. CGH with genomic DNA prepared from these cell lines as probes successfully identified genomic gains and/or losses in chromosomal regions encoding putative genes associated with drug resistance and/or thermoresistance. These genes included various members of the families of ABC transporters and molecular chaperones. The importance of these cell variant-specific genomic imbalances in the development of MDR and thermoresistance is discussed and remains to be elucidated. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:752 / 758
页数:7
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