Evaluation of arrayed primer extension for TP53 mutation detection in breast and ovarian carcinomas

被引:17
作者
Kringen, P
Bergamaschi, A
Due, EU
Wang, Y
Tagliabue, E
Nesland, JM
Nehman, A
Tönisson, N
Borresen-Dale, AL [1 ]
机构
[1] Norwegian Radium Hosp, Dept Genet, N-0310 Oslo, Norway
[2] Ist Nazl Studio & Cura Tumori, I-20133 Milan, Italy
[3] Univ Tartu, EE-50090 Tartu, Estonia
关键词
D O I
10.2144/000112000
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Mutations in the tumor suppressor gene TP53 are associated with a wide range of different cancers and may have prognostic and therapeutic implications. Methods for rapid and sensitive detection of mutations in this gene are therefore required. In order to make screening more effective, a commercially available TP53 genotyping microarray from Asper Biotech has been constructed by arrayed primer extension (APEX). The present study is the first report that blindly evaluates the efficiency of the second generation APEXTP53 genotype chip outside the Asper laboratory and compares it to temporal temperature gradient electrophoresis (TTGE) and sequencing of TP53 for mutation detection in ovarian and breast cancer samples. All nucleotides in the TP53 gene from exon 2-9 are included on the chip by synthesis and application of sequence-specific oligonucleotides. The chip was validated by screening 48 breast and 11 ovarian cancer cases, all of which had previously been analyzed by TTGE and sequencing. APEX scored 17 of 20 sequence variants, missing one deletion, one insertion, and a missense mutation. Resequencing efficiency using APEX was 92% for both DNA strands and 99.5% for sense and/or antisense strand. We conclude that the APEX TP53 microarray is a robust, rapid, and comprehensive screening tool for sequence alterations in tumors.
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页码:755 / 761
页数:7
相关论文
共 17 条
[1]   Specific P53 mutations are associated with de novo resistance to doxorubicin in breast cancer patients [J].
Aas, T ;
Borresen, AL ;
Geisler, S ;
SmithSorensen, B ;
Johnsen, H ;
Varhaug, JE ;
Akslen, LA ;
Lonning, PE .
NATURE MEDICINE, 1996, 2 (07) :811-814
[2]  
Aas Turid, 1994, Tidsskrift for den Norske Laegeforening, V114, P668
[3]   COMPLETE SEQUENCING OF THE P53 GENE PROVIDES PROGNOSTIC INFORMATION IN BREAST-CANCER PATIENTS, PARTICULARLY IN RELATION TO ADJUVANT SYSTEMIC THERAPY AND RADIOTHERAPY [J].
BERGH, J ;
NORBERG, T ;
SJOGREN, S ;
LINDGREN, A ;
HOLMBERG, L .
NATURE MEDICINE, 1995, 1 (10) :1029-1034
[4]  
Berns EMJJ, 2000, CANCER RES, V60, P2155
[5]  
BORENSENDALE AL, 2003, HUM MUTAT, V21, P292
[6]   TP53 MUTATIONS AND BREAST-CANCER PROGNOSIS - PARTICULARLY POOR SURVIVAL RATES FOR CASES WITH MUTATIONS IN THE ZINC-BINDING DOMAINS [J].
BORRESEN, AL ;
ANDERSEN, TI ;
EYFJORD, JE ;
CORNELIS, RS ;
THORLACIUS, S ;
BORG, A ;
JOHANSSON, U ;
THEILLET, C ;
SCHERNECK, S ;
HARTMAN, S ;
CORNELISSE, CJ ;
HOVIG, E ;
DEVILEE, P .
GENES CHROMOSOMES & CANCER, 1995, 14 (01) :71-75
[7]  
Borresen-Dale AL, 1998, CLIN CANCER RES, V4, P203
[8]   The combination of p53 mutation and neu/erbB-2 amplification is associated with poor survival in node-negative breast cancer [J].
Bull, SB ;
Ozcelik, H ;
Pinnaduwage, D ;
Blackstein, ME ;
Sutherland, DAJ ;
Pritchard, KI ;
Tzontcheva, AT ;
Sidlofsky, S ;
Hanna, WM ;
Qizilbash, AH ;
Tweeddale, ME ;
Fine, S ;
McCready, DR ;
Andrulis, IL .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (01) :86-96
[9]   Integration of combined heteroduplex/restriction fragment length polymorphism analysis on an electrophoresis microchip for the detection of hereditary haemochromatosis [J].
Footz, T ;
Somerville, MJ ;
Tomaszewski, R ;
Elyas, B ;
Backhouse, CJ .
ANALYST, 2004, 129 (01) :25-31
[10]  
Geisler S, 2003, CLIN CANCER RES, V9, P5582