Increase in tumor GADD153 mRNA level following treatment correlates with response to paclitaxel

被引:11
作者
de las Alas, MM
Christen, RD
Gately, DP
Weiner, DE
Benbatoul, K
Kirmani, S
D'Agostino, HR
Plaxe, SC
Darrah, D
McClay, EF
Aebi, S
Howell, SB
Los, G
机构
[1] Univ Calif San Diego, Canc Ctr 0058, Dept Biomed Sci, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Surg, La Jolla, CA 92093 USA
关键词
GADD153; MDR1; paclitaxel;
D O I
10.1007/s002800051006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We investigated the relationship between the basal and treatment-induced change in the tumor expression of the drug resistance gene MDR1 and the cellular injury response gene GADD153, and clinical response to paclitaxel treatment. Methods: MDR1 and GADD153 mRNA levels were measured by reverse transcriptase polymerase chain reaction (RT-PCR) in tumor samples obtained by fine needle aspiration biopsy from 14 patients before and 24 h after paclitaxel infusion. Results: There was no difference between responders and non-responders with respect to either the basal MDR1 mRNA level or the change in MDR1 mRNA level at 24 h after treatment (P = 0.464). Likewise. there was no difference in basal GADD153 mRNA level between responders and non-responders. However, there was a significantly greater increase in GADD153 mRNA at 24 h in responders compared with non-responders (P = 0.005). An increase in GADD153 mRNA level of 1.5-fold or higher predicted response with a sensitivity of 86% and a specificity of 100%. Conclusions: An increase in GADD153 mRNA level reflects chemotherapy-induced damage sufficient to be manifest as a clinically detectable reduction in tumor volume. Measurement of the change in GADD153 mRNA level successfully identified patients destined to respond as early as 24 h post-treatment.
引用
收藏
页码:381 / 388
页数:8
相关论文
共 33 条
[1]  
Davis LG., 1986, Basic Methods in Molecular Biology
[2]  
DELASALAS M, 1996, P AN M AM SOC CLIN, V37, P571
[3]  
Delmastro DA, 1997, CANCER CHEMOTH PHARM, V39, P245
[4]   CELL-MEDIATED IMMUNITY TO HUMAN MALIGNANT CELLS - BRIEF REVIEW AND FURTHER STUDIES WITH 2 GYNECOLOGIC TUMORS [J].
DISAIA, PJ ;
RUTLEDGE, FN ;
SMITH, JP ;
SINKOVICS, JG .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1972, 114 (07) :979-+
[5]  
Eymin B, 1997, CANCER RES, V57, P686
[6]   DNA DAMAGE-INDUCIBLE TRANSCRIPTS IN MAMMALIAN-CELLS [J].
FORNACE, AJ ;
ALAMO, I ;
HOLLANDER, MC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) :8800-8804
[7]   MAMMALIAN GENES COORDINATELY REGULATED BY GROWTH ARREST SIGNALS AND DNA-DAMAGING AGENTS [J].
FORNACE, AJ ;
NEBERT, DW ;
HOLLANDER, MC ;
LUETHY, JD ;
PAPATHANASIOU, M ;
FARGNOLI, J ;
HOLBROOK, NJ .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (10) :4196-4203
[8]   Paclitaxel activation of the GADD153 promoter through a cellular injury response element containing an essential Sp1 binding site [J].
Gately, DP ;
Howell, SB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (34) :20588-20593
[9]   INDUCTION OF THE GROWTH ARREST AND DNA DAMAGE-INDUCIBLE GENE GADD153 BY CISPLATIN IN-VITRO AND IN-VIVO [J].
GATELY, DP ;
JONES, JA ;
CHRISTEN, R ;
BARTON, RM ;
LOS, G ;
HOWELL, SB .
BRITISH JOURNAL OF CANCER, 1994, 70 (06) :1102-1106
[10]   Cisplatin and taxol activate different signal pathways regulating cellular injury-induced expression of GADD153 [J].
Gately, DP ;
Sharma, A ;
Christen, RD ;
Howell, SB .
BRITISH JOURNAL OF CANCER, 1996, 73 (01) :18-23