Gately D P, Jones J A, Christen R, Barton R M, Los G, Howell S B
Department of Biomedical Sciences, University of California, San Diego, La Jolla.
Br J Cancer. 1994 Dec;70(6):1102-6. doi: 10.1038/bjc.1994.455.
The inability to assess the extent of tumour damage immediately following treatment is a major clinical obstacle to improving the management of cancer patients. Normally, the effectiveness of chemotherapy or radiation therapy cannot be determined for at least several weeks after treatment. We studied the increase in mRNA of the growth arrest and DNA damage-inducible gene GADD153 in human 2008 ovarian carcinoma cells in vitro and in vivo to determine whether treatment-induced increases in the level of GADD153 mRNA could be used as a marker of the extent of tumour damage. GADD153 mRNA was increased in a transient, dose-dependent manner by cisplatin (DDP) when the tumour cells were grown both in vitro and as tumour xenografts in nude mice. The magnitude of induction of GADD153 mRNA did not vary significantly between different 2008 xenografts treated with equal doses of DDP, and GADD153 mRNA induction correlated with the degree of in vitro cytotoxicity for two different schedules of drug exposure. DDP increased GADD153 mRNA levels in melanoma and head and neck xenograft models as well. We conclude that the increase in GADD153 mRNA can be used to detect tumour injury at time points as short as 24 h after administration of DDP.
治疗后无法立即评估肿瘤损伤程度是改善癌症患者管理的主要临床障碍。通常,化疗或放疗的效果在治疗后至少几周内无法确定。我们在体外和体内研究了人2008卵巢癌细胞中生长停滞和DNA损伤诱导基因GADD153的mRNA增加情况,以确定治疗诱导的GADD153 mRNA水平升高是否可作为肿瘤损伤程度的标志物。当肿瘤细胞在体外生长以及在裸鼠体内作为肿瘤异种移植物生长时,顺铂(DDP)可使GADD153 mRNA以瞬时、剂量依赖性方式增加。用等量DDP处理的不同2008异种移植物之间,GADD153 mRNA的诱导幅度没有显著差异,并且对于两种不同的药物暴露方案,GADD153 mRNA诱导与体外细胞毒性程度相关。DDP在黑色素瘤和头颈部异种移植模型中也增加了GADD153 mRNA水平。我们得出结论,GADD153 mRNA的增加可用于在给予DDP后短至24小时的时间点检测肿瘤损伤。