Induced resistance in the human non small cell lung carcinoma (NCI-H460) cell line in vitro by anticancer drugs

被引:97
作者
Pesic, M
Markovic, JZ
Jankovic, D
Kanazir, S
Markovic, ID
Rakic, L
Ruzdijic, S
机构
[1] Inst Biol Res, Dept Neurobiol & Immunol, Mol Neurobiol Lab, Belgrade 11060, Serbia Monteneg
[2] Univ Belgrade, Fac Med, Belgrade 11000, Serbia Monteneg
[3] Serbian Acad Arts & Sci, Belgrade 11000, Serbia Monteneg
关键词
human non-small cell lung carcinoma (NSCLC); doxorubicin; pacilitaxel; multidrug resistance; verapamil; curcumin; P-glycoprotein; doxorubicin efflux; RT-PCR; glutathione-S-transferase;
D O I
10.1179/joc.2006.18.1.66
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Exposure of human non-small cell lung cancer cells (NCI-H460) to gradually increasing concentrations of doxorubicin resulted in the appearance of a new cell line (NCI-H460/R) that was resistant to doxorubicin (96.2-fold) and cross-resistant to etoposide, paclitaxel, vinblastine and epirubicin. Slight cross-resistance to two MDR-unrelated drugs 8-Cl-cAMP and sulfinosine was observed. Flow cytometry analysis showed that the accumulation of doxorubicin in the resistant cells was 88.4% lower than in the parental cells. Also, verapamil significantly decreased the efflux rate in NCI-H460 and NCI-H460/R cells, whereas curcumin inhibited the efflux in NCI-H460 cells only. Gene expression data confirmed the induction of mdr1(P-gp), as judged by the observed 15-fold increase in its mRNA concentration in doxorubicin-resistant NCI-H460/R cells. In contrast, mrp1 and lrp expression was unaffected by the doxorubicin resistance. Further work should develop a rationale for a novel treatment of NSCLC with appropriate modulators of resistance aimed at improving the outcome of the acquired drug resistance.
引用
收藏
页码:66 / 73
页数:8
相关论文
共 30 条
[11]   Role of glutathione S-transferase P1, P-glycoprotein and multidrug resistance-associated protein 1 in acquired doxorubicin resistance [J].
Harbottle, A ;
Daly, AK ;
Atherton, K ;
Campbell, FC .
INTERNATIONAL JOURNAL OF CANCER, 2001, 92 (06) :777-783
[12]  
HORWITZ SB, 1992, TRENDS PHARMACOL SCI, V13, P134
[13]  
Izquierdo MA, 1996, INT J CANCER, V65, P230
[14]   Vaults are up-regulated in multidrug-resistant cancer cell lines [J].
Kickhoefer, VA ;
Rajavel, KS ;
Scheffer, GL ;
Dalton, WS ;
Scheper, RJ ;
Rome, LH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (15) :8971-8974
[15]   Multidrug resistance (MDR) in cancer - Mechanisms, reversal using modulators of MDR and the role of MDR modulators in influencing the pharmacokinetics of anticancer drugs [J].
Krishna, R ;
Mayer, LD .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2000, 11 (04) :265-283
[16]  
MUNEYAMA K, 1971, BIOCHEMISTRY-US, V10, P2390
[17]   TAXOL BINDS TO POLYMERIZED TUBULIN INVITRO [J].
PARNESS, J ;
HORWITZ, SB .
JOURNAL OF CELL BIOLOGY, 1981, 91 (02) :479-487
[18]   EVOLUTIONARY CONSERVATION IN THE UNTRANSLATED REGIONS OF ACTIN MESSENGER-RNAS - DNA-SEQUENCE OF A HUMAN BETA-ACTIN CDNA [J].
PONTE, P ;
NG, SY ;
ENGEL, J ;
GUNNING, P ;
KEDES, L .
NUCLEIC ACIDS RESEARCH, 1984, 12 (03) :1687-1696
[19]  
Pronzato P, 2001, LUNG CANCER-J IASLC, V34, pS57
[20]   P-GLYCOPROTEIN AND ALTERATIONS IN THE GLUTATHIONE GLUTATHIONE-PEROXIDASE CYCLE UNDERLIE DOXORUBICIN RESISTANCE IN HL-60-R, A SUBCLONE OF THE HL-60 HUMAN LEUKEMIA-CELL LINE [J].
RAGHU, G ;
PIERREJEROME, M ;
DORDAL, MS ;
SIMONIAN, P ;
BAUER, KD ;
WINTER, JN .
INTERNATIONAL JOURNAL OF CANCER, 1993, 53 (05) :804-811