Altered DNA methylation is associated with docetaxel resistance in human breast cancer cells

被引:54
作者
Kastl, Lena [1 ]
Brown, Iain [1 ]
Schofield, Andrew C. [1 ]
机构
[1] Univ Aberdeen, Sch Med, Coll Life Sci & Med, Sch Med & Dent, Aberdeen AB25 2ZD, Scotland
关键词
breast cancer; chemotherapy; DNA methylation; drug resistance; MESSENGER-RNA EXPRESSION; METHYLTRANSFERASES DNMT3A; HISTONE DEACETYLASE; ESTROGEN-RECEPTOR; OVARIAN-CANCER; BETA-TUBULIN; GENE; HYPERMETHYLATION; HYPOMETHYLATION; DEMETHYLATION;
D O I
10.3892/ijo_00000607
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Docetaxel is an effective chemotherapy drug to treat breast cancer but the underlying molecular mechanisms of drug resistance are not fully understood DNA methylation is an epigenetic event, involved in the control of gene expression. which is known to play an important role in cancer and chemotherapy drug resistance. To investigate the role of DNA methylation in docetaxel resistance in breast cancer we used two human breast cancer cell lines (MCF-7 and MDA-MB-231) that were made resistant to docetaxel Docetaxel-resistant sub-lines were treated with different concentrations of decitabine Global methylation and DNA methyltransferase (DNMT) activity was measured using an ELISA-based assay Quantitative real-time PCR was used to study DNMT acne expression Cell viability was studied by MTT assay Global methylation was increased in MCF-7 but not significantly changed in MDA-MB-231 docetaxel-resistant cells Decreased DNMT activity and decreased DNMT1 and DNMT3b mRNA expression was associated with docetaxel resistance in both cell lines. To investigate how the components of the DNA methylation machinery may contribute towards docetaxel resistance. decitabine (5-aza-2'-deoxycytidine). an inhibitor of DNA methylation, was used Decitabine treatment decreased global methylation. DNMT activity and DNMT1, DNMT3a and DNMT3b mRNA expression in MDA-MB-23 I docetaxel-resistant cells In contrast. decitabine-treated MCF-7 docetaxel-resistant cells showed increased DNMT1, DNMT3a and DNMT3b mRNA expression indicating a cell line specific effect of decitabine Decitabine treatment increased resistance in MCF-7 docetaxel-resistant cells and in the parental MCF-7 and MDA-MB231 docetaxel-sensitive cell lines, however. it did not alter response to docetaxel in MDA-MB-231 docetaxel-resistant cells This study demonstrates that changes in the DNA methylation machinery are associated with resistance to docetaxel in breast cancer cells. The use of epigenetic therapies. as a strategy to overcome drug resistance, needs to be investigated more fully to determine their effectiveness in different cancers and for different chemotherapy drugs.
引用
收藏
页码:1235 / 1241
页数:7
相关论文
共 33 条
[1]   Reduced expression of p27 is a novel mechanism of docetaxel resistance in breast cancer cells [J].
Brown, I ;
Shalli, K ;
McDonald, SL ;
Moir, SE ;
Hutcheon, AW ;
Heys, SD ;
Schofield, AC .
BREAST CANCER RESEARCH, 2004, 6 (05) :R601-R607
[2]   Role of DNA hypomethylation in the development of the resistance to doxorubicin in human MCF-7 breast adenocarcinoma cells [J].
Chekhun, VF ;
Kulik, GI ;
Yurchenko, OV ;
Tryndyak, VP ;
Todor, IN ;
Luniv, LS ;
Tregubova, NA ;
Pryzimirska, TV ;
Montgomery, B ;
Rusetskaya, NV ;
Pogribny, IP .
CANCER LETTERS, 2006, 231 (01) :87-93
[3]   Correlation between CpG methylation profiles and hormone receptor status in breast cancers [J].
Feng, Weiwei ;
Shen, Lanlan ;
Wen, Sijin ;
Rosen, Daniel G. ;
Jelinek, Jaroslav ;
Hu, Xin ;
Huan, Shaoyi ;
Huang, Miao ;
Liu, Jinsong ;
Sahin, Aysegul A. ;
Hunt, Kelly K. ;
Bast, Robert C., Jr. ;
Shen, Yu ;
Issa, Jean-Pierre J. ;
Yu, Yinhua .
BREAST CANCER RESEARCH, 2007, 9 (04)
[4]   Sensitization for death receptor- or drug-induced apoptosis by re-expression of caspase-8 through demethylation or gene transfer [J].
Fulda, S ;
Küfer, MU ;
Meyer, E ;
van Valen, F ;
Dockhorn-Dworniczak, B ;
Debatin, KM .
ONCOGENE, 2001, 20 (41) :5865-5877
[5]   DNA methyltransferase inhibitors - state of the art [J].
Goffin, J ;
Eisenhauer, E .
ANNALS OF ONCOLOGY, 2002, 13 (11) :1699-1716
[6]   Timing is everything: Order of administration of 5-aza 2′ deoxycytidine, trichostatin A and tamoxifen changes estrogen receptor mRNA expression and cell sensitivity [J].
Hostetter, Christine L. ;
Licata, Lauren A. ;
Keen, Judith Clancy .
CANCER LETTERS, 2009, 275 (02) :178-184
[7]   Genomic organization and promoter analysis of the Dnmt3b gene [J].
Ishida, C ;
Ura, K ;
Hirao, A ;
Sasaki, H ;
Toyoda, A ;
Sakaki, Y ;
Niwa, H ;
Li, E ;
Kaneda, Y .
GENE, 2003, 310 :151-159
[8]  
Izutsu N, 2008, INT J ONCOL, V32, P1227
[9]   Randomized phase III study of docetaxel compared with paclitaxel in metastatic breast cancer [J].
Jones, SE ;
Erban, J ;
Overmoyer, B ;
Budd, GT ;
Hutchins, L ;
Lower, E ;
Laufman, L ;
Sundaram, S ;
Urba, WJ ;
Pritchard, KI ;
Mennel, R ;
Richards, D ;
Olsen, S ;
Meyers, ML ;
Ravdin, PM .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (24) :5542-5551
[10]  
KASTL L, MOL CELL PR IN PRESS