CONSTANT DENATURANT GEL-ELECTROPHORESIS AS A RAPID SCREENING TECHNIQUE FOR P53 MUTATIONS

被引:211
作者
BORRESEN, AL
HOVIG, E
SMITHSORENSEN, B
MALKIN, D
LYSTAD, S
ANDERSEN, TI
NESLAND, JM
ISSELBACHER, KJ
FRIEND, SH
机构
[1] MASSACHUSETTS GEN HOSP,CTR CANC,CHARLESTON,MA 02129
[2] NORWEGIAN RADIUM HOSP,INST CANC RES,DEPT PATHOL,OSLO 3,NORWAY
[3] HARVARD UNIV,CHILDRENS HOSP,DANA FARBER CANC INST,BOSTON,MA 02115
[4] HARVARD UNIV,SCH MED,BOSTON,MA 02115
关键词
TUMOR-SUPPRESSOR GENE; DNA SCREENING; LOSS OF HETEROZYGOSITY; CHROMOSOME-17; BREAST CANCER;
D O I
10.1073/pnas.88.19.8405
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
At present, mutation of the p53 gene appears to be the most common genetic alteration found in human cancers. These mutations can occur within many different regions of the gene. We have developed a modification of denaturing gradient gel electrophoresis termed "constant denaturant gel electrophoresis" (CDGE), which provides a rapid and sensitive method to screen the four conserved regions within the p53 gene where the majority of p53 mutations have been reported. The sensitivity of CDGE was first tested with known p53 mutations in all four conserved regions. The CDGE technique was then used to screen 32 breast carcinomas that had been analyzed by immunohistochemical methods for altered p53 protein levels and whose DNA had already been shown to have loss of heterozygosity for a chromosome 17p marker. By immunostaining techniques, only 6 of the 32 tumors had elevated p53 expression. However, CDGE detected p53 mutations in 11 of the 32 tumors. DNA sequence analysis was performed to determine the nucleotide positions of these mutations in all 11 samples. Loss of heterozygosity for the pYNZ22 or p144D6 markers did not associate with either the loss of heterozygosity at the p53 locus or the mutations detected by CDGE. We conclude that CDGE is a rapid and effective technique to screen for p53 mutations.
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收藏
页码:8405 / 8409
页数:5
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