Increased expression of human DNA repair genes, XRCC1, XRCC3 and RAD51, in radioresistant human KB carcinoma cell line N10

被引:39
作者
Yanagisawa, T
Urade, M
Yamamoto, Y
Furuyama, J
机构
[1] Hyogo Coll Med, Dept Dent & Oral Surg, Nishinomiya, Hyogo 6638501, Japan
[2] Hyogo Coll Med, Dept Genet, Nishinomiya, Hyogo 6638501, Japan
关键词
KB carcinoma cell line; radioresistance; human DNA repair genes (XRCC1; XRCC3; RAD51);
D O I
10.1016/S1368-8375(98)00045-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The radioresistant N10 and parental KB cell lines were examined for the expression of human DNA repair genes which were related to the repair of radiation-induced DNA damage by northern blot analysis using five kinds of DNA probes (XRCC1, XRCC3, XRCCS, RAD51, RAD52). In the unirradiated condition, N10 cells showed higher expression of XRCC1, XRCC3 and RAD51 mRNA than did KB cells. The X-irradiation induced a time-dependent increase in the mRNA levels of XRCC3 and RADS1 in both cell lines with a maximum at 2 h postirradiation. The XRCC1 mRNA in N10 was maintained at the same level even after irradiation, whereas that in KB was decreased after irradiation. There was no difference in the expression of XRCC5 and RAD52 mRNA between N10 and KB cells in both unirradiated and irradiated conditions. From these findings, it was suggested that XRCC1, XRCC3 and RADS1 contribute to the radioresistance in cell line N10. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:524 / 528
页数:5
相关论文
共 30 条
[1]   CHROMOSOMAL LOCATION AND EXPRESSION OF THE GENES-CODING FOR KU P70 AND P80 IN HUMAN CELL-LINES AND NORMAL-TISSUES [J].
CAI, QQ ;
PLET, A ;
IMBERT, J ;
LAFAGEPOCHITALOFF, M ;
CERDAN, C ;
BLANCHARD, JM .
CYTOGENETICS AND CELL GENETICS, 1994, 65 (04) :221-227
[2]   XRCC1 polypeptide interacts with DNA polymerase beta and possibly poly(ADP-ribose) polymerase, and DNA ligase III is a novel molecular 'nick-sensor' in vitro [J].
Caldecott, KW ;
Aoufouchi, S ;
Johnson, P ;
Shall, S .
NUCLEIC ACIDS RESEARCH, 1996, 24 (22) :4387-4394
[3]   AN INTERACTION BETWEEN THE MAMMALIAN DNA-REPAIR PROTEIN XRCC1 AND DNA LIGASE-III [J].
CALDECOTT, KW ;
MCKEOWN, CK ;
TUCKER, JD ;
LJUNGQUIST, S ;
THOMPSON, LH .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (01) :68-76
[4]  
EAGLE H, 1955, P SOC EXP BIOL MED, V89, P362
[5]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[6]  
GAME JC, 1993, SEMIN CANCER BIOL, V4, P73
[7]   LOCALIZATION OF A DNA-REPAIR GENE (XRCC5) INVOLVED IN DOUBLE-STRAND-BREAK REJOINING TO HUMAN CHROMOSOME-2 [J].
JEGGO, PA ;
HAFEZPARAST, M ;
THOMPSON, AF ;
BROUGHTON, BC ;
KAUR, GP ;
ZDZIENICKA, MZ ;
ATHWAL, RS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (14) :6423-6427
[8]  
KAPP LN, 1992, AM J HUM GENET, V51, P45
[9]  
KIRCHGESSNER CU, 1993, CANCER RES, V53, P6011
[10]   STRUCTURAL AND FUNCTIONAL CONSERVATION OF 2 HUMAN HOMOLOGS OF THE YEAST DNA-REPAIR GENE RAD6 [J].
KOKEN, MHM ;
REYNOLDS, P ;
JASPERSDEKKER, I ;
PRAKASH, L ;
PRAKASH, S ;
BOOTSMA, D ;
HOEIJMAKERS, JHJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (20) :8865-8869