Dose-dependent and independent temporal patterns of gene responses to ionizing radiation in normal and tumor cells and tumor xenografts

被引:55
作者
Khodarev, NN
Park, JO
Yu, JQ
Gupta, N
Nodzenski, E
Roizman, B [1 ]
Weichselbaum, RR
机构
[1] Univ Chicago, Marjorie B Kovler Viral Oncol Labs, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Radiat & Cellular Oncol, Chicago, IL 60637 USA
关键词
cDNA arrays; gene clusters; time course; radiotherapy; transcription;
D O I
10.1073/pnas.211443698
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
U87 cells derived from human malignant gliomas and growth-arrested human embryonic lung (HEL) fibroblasts were examined with respect to their response to ionizing radiation by profiling their RNAs. In the first series of experiments, cells grown in vitro were harvested and the RNAs were extracted 5 h after exposure to 1, 3, or 10 Gy. In the second series of experiments the U87 tumors were implanted in nude mice and subjected to the same doses of irradiation. The xenografts were harvested at 1, 5, or 24 h after irradiation and subjected to the same analyses. We observed and report on (i) cell-type common and cell-type specific responses, (ii) genes induced at low levels of irradiation but not at higher doses, (iii) temporal patterns of gene response in U87 xenografts that varied depending on radiation dose and temporal patterns of response that were similar at all doses tested, (iv) significantly higher up-regulation of cells in xenografts than in in vitro cultures, and (v) genes highly up-regulated by radiation. The responding genes could be grouped into nine functional clusters. The representation of the nine clusters was to some extent dependent on dose and time after irradiation. The results suggest that clinical outcome of ionizing radiation treatment may benefit significantly by taking into account both cell-type and radiation-dose specificity of cellular responses.
引用
收藏
页码:12665 / 12670
页数:6
相关论文
共 29 条
[1]   Fluorescent cDNA microarray hybridization reveals complexity and heterogeneity of cellular genotoxic stress responses [J].
Amundson, SA ;
Bittner, M ;
Chen, YD ;
Trent, J ;
Meltzer, P ;
Fornace, AJ .
ONCOGENE, 1999, 18 (24) :3666-3672
[2]  
Bradley JD, 1999, CLIN CANCER RES, V5, P1517
[3]   STRUCTURAL MODIFICATIONS OF HUMAN BETA-2 MICROGLOBULIN TREATED WITH OXYGEN-DERIVED RADICALS [J].
CAPEILLEREBLANDIN, C ;
DELAVEAU, T ;
DESCAMPSLATSCHA, B .
BIOCHEMICAL JOURNAL, 1991, 277 :175-182
[4]  
CRELLIN RP, 1993, CLIN ONCOL, V5, P5139
[5]   Protein phosphatases regulate DNA-dependent protein kinase activity [J].
Douglas, P ;
Moorhead, GBG ;
Ye, RQ ;
Lees-Miller, SP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (22) :18992-18998
[6]   Protein interactions of the MLL PHD fingers modulate MLL target gene regulation in human cells [J].
Fair, K ;
Anderson, M ;
Bulanova, E ;
Mi, HF ;
Tropschug, M ;
Diaz, MO .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (10) :3589-3597
[7]   Fundamentals of DNA hybridization arrays for gene expression analysis [J].
Freeman, WM ;
Robertson, DJ ;
Vrana, KE .
BIOTECHNIQUES, 2000, 29 (05) :1042-+
[8]  
Hall E., 2000, RADIOBIOLOGY RADIOLO, V5th, P5
[9]   INCREASED TUMOR NECROSIS FACTOR-ALPHA MESSENGER-RNA AFTER CELLULAR EXPOSURE TO IONIZING-RADIATION [J].
HALLAHAN, DE ;
SPRIGGS, DR ;
BECKETT, MA ;
KUFE, DW ;
WEICHSELBAUM, RR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (24) :10104-10107
[10]   The CREC family, a novel family of multiple EF-hand, low-affinity Ca2+-binding proteins localised to the secretory pathway of mammalian cells [J].
Honoré, B ;
Vorum, H .
FEBS LETTERS, 2000, 466 (01) :11-18