Predictive value of GADD153, p21 and c-Jun for chemotherapy response in gastric cancer

被引:9
作者
Akatsu, Yukako
Saikawa, Yoshiro
Kubota, Tetsuro
Akatsu, Tomotaka
Yoshida, Masashi
Kitagawa, Yuko
Otani, Yoshihide
Kumai, Koichiro
Kitajima, Masaki
机构
[1] Keio Univ, Sch Med, Dept Surg, Tokyo 1608582, Japan
[2] Keio Univ, Sch Med, Ctr Diagnost & Therapeut Endoscopy, Tokyo 1608582, Japan
来源
CANCER SCIENCE | 2007年 / 98卷 / 05期
关键词
D O I
10.1111/j.1349-7006.2007.00435.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We sought to determine whether changes in the expression of early response genes (GADD153, p21 and c-Jun) are indicators of chemotherapy response in gastric cancer. Three human gastric cancer cell lines were exposed to 5-fluorouracil or cisplatin in vitro. Xenografts of TMK-1 cells in nude mice were also treated with 5-fluorouracil or cisplatin in vivo. For each of these treatments, we tested for a correlation between early gene expression levels and inhibition ratios derived at a later time. A 5-fluorouracil derivative, S-1, and cisplatin were administered to 12 patients with advanced gastric cancer for 3 weeks. Gene expression levels were measured using biopsy specimens obtained by endoscopy soon after initiation of chemotherapy. There was a significant correlation between expression levels of these genes at 24 h and inhibition ratios at 72 h in vitro. Cut-off values determined from receiver-operating characteristic curves were 1.3 for GADD153, 1.8 for p21 and 2.1 for c-Jun There was also a significant correlation between gene expression levels at 2 days and inhibition ratios at 21 days in vivo. Cut-off values were 1.8 for GADD153, 1.9 for p21 and 2.2 for c-Jun. Levels of early response gene expression in patients showing progressive disease were significantly lower than those in patients with partial response. Changes in the expression of the three early response genes soon after drug administration could improve predictions of the final outcome of chemotherapy in gastric cancer.
引用
收藏
页码:707 / 715
页数:9
相关论文
共 25 条
[1]   Paclitaxel-based chemoradiotherapy in localized gastric carcinoma: Degree of pathologic response and not clinical parameters dictated patient outcome [J].
Ajani, JA ;
Mansfield, PF ;
Crane, CH ;
Wu, TT ;
Lunagomez, S ;
Lynch, PM ;
Janjan, N ;
Feig, B ;
Faust, J ;
Yao, JC ;
Nivers, R ;
Morris, J ;
Pisters, PW .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (06) :1237-1244
[2]   Multi-institutional trial of preoperative chemoradiotherapy in patients with potentially resectable gastric carcinoma [J].
Ajani, JA ;
Mansfield, PF ;
Janjan, N ;
Morris, J ;
Pisters, PW ;
Lynch, PM ;
Feig, B ;
Myerson, R ;
Nivers, R ;
Cohen, DS ;
Gunderson, LL .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (14) :2774-2780
[3]   Transcriptional activation by p53, but not induction of the p21 gene, is essential for oncogene-mediated apoptosis [J].
Attardi, LD ;
Lowe, SW ;
Brugarolas, J ;
Jacks, T .
EMBO JOURNAL, 1996, 15 (14) :3693-3701
[4]  
BUSCHER M, 1988, ONCOGENE, V3, P301
[5]  
Chung YS, 1997, CANCER, V80, P1
[6]  
ELDEIRY WS, 1994, CANCER RES, V54, P1169
[7]  
Friedman AD, 1996, CANCER RES, V56, P3250
[8]   Induction of thymidine phosphorylase by interferon and taxanes occurs only in human cancer cells with low thymidine phosphorylase activity [J].
Fukushima, M ;
Okabe, H ;
Takechi, T ;
Ichikawa, W ;
Hirayama, R .
CANCER LETTERS, 2002, 187 (1-2) :103-110
[9]  
FUTSCHER BW, 1990, CANCER RES, V50, P62
[10]   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