Multiplex tetra-primer amplification refractory mutation system PCR to detect 6 common germline mutations of the MUTYH gene associated with polyposis and colorectal cancer

被引:33
作者
Piccioli, P
Sierra, M
Gismondi, V
Pedemonte, S
Loiacono, F
Lastraioli, S
Bertario, L
De Angioletti, M
Varcsco, L
Notaro, R
机构
[1] Ist Nazl Ric Canc, Lab Human Genet, IST, I-16132 Genoa, Italy
[2] Ist Nazl Ric Canc, Hereditary Tumors Unit, IST, I-16132 Genoa, Italy
[3] Ist Nazl Tumori, Prevent Pred Med Unit, I-20133 Milan, Italy
[4] CNR, Ist Genet & Biofis Adirano Buzzati Traverso, I-80125 Naples, Italy
关键词
D O I
10.1373/clinchem.2005.060137
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: We describe a simple tetra-primer amplification refractory mutation system PCR (T-ARMS-PCR) for detecting MUTYH mutations, which are associated with colorectal adenomas and colorectal cancer. Methods: We designed specific T-ARMS-PCR assays for 6 mutations (Y165C, G382D, 1395_7delGGA, Y90X, 1103de1C, and R231H) selected on the basis of the frequency of their occurrence. We also designed a set of 3 multiplex T-ARMS PCR assays, each for detection of 2 mutations. We tested DNA samples from patients with attenuated or classic adenomatous polyposis coli and no detectable APC germline mutations. Results: All mutations were easily detected with both the specific and multiplex T-ARMS-PCR assays. Results were confirmed by DNA HPLC analysis in all 54 patients, and each mutation was confirmed by direct DNA sequencing. Conclusions: T-ARMS-PCR does not require any special equipment, and it provides rapid, reproducible, and cost-effective detection of common MUTYH mutations. Multiplex T-ARMS-PCR allows the detection of 6 common MUTYH mutations with use of as few as 3 single tube PCR reactions. It could be useful to carry out large population-based epidemiologic studies. (c) 2006 American Association for Clinical Chemistry.
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收藏
页码:739 / 743
页数:5
相关论文
共 22 条
[1]  
Aceto Gitana, 2005, Hum Mutat, V26, P394, DOI 10.1002/humu.9370
[2]   Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors [J].
Al-Tassan, N ;
Chmiel, NH ;
Maynard, J ;
Fleming, N ;
Livingston, AL ;
Williams, GT ;
Hodges, AK ;
Davies, DR ;
David, SS ;
Sampson, JR ;
Cheadle, JR .
NATURE GENETICS, 2002, 30 (02) :227-232
[3]   Colorectal cancer and inherited mutations in base-excision repair [J].
Chow, E ;
Thirlwell, C ;
Macrae, F ;
Lipton, L .
LANCET ONCOLOGY, 2004, 5 (10) :600-606
[4]   Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk [J].
Croitoru, ME ;
Cleary, SP ;
Di Nicola, N ;
Manno, M ;
Selander, T ;
Aronson, M ;
Redston, M ;
Cotterchio, M ;
Knight, J ;
Gryfe, R ;
Gallinger, S .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (21) :1631-1634
[5]   The potential for increased clinical sensitivity in genetic testing for polyposis colorectal cancer through the analysis of MYH mutations in North American patients [J].
Eliason, K ;
Hendrickson, BC ;
Judkins, T ;
Norton, M ;
Leclair, B ;
Lyon, E ;
Ward, B ;
Noll, W ;
Scholl, T .
JOURNAL OF MEDICAL GENETICS, 2005, 42 (01) :95-96
[6]   Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients [J].
Enholm, S ;
Hienonen, T ;
Suomalainen, A ;
Lipton, L ;
Tomlinson, I ;
Kärjä, V ;
Eskelinen, M ;
Mecklin, JP ;
Karhu, A ;
Järvinen, HJ ;
Aaltonen, LA .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 163 (03) :827-832
[7]   Germline susceptibility to colorectal cancer due to base-excision repair gene defects [J].
Farrington, SM ;
Tenesa, A ;
Barnetson, R ;
Wiltshire, A ;
Prendergast, J ;
Porteous, M ;
Campbell, H ;
Farrington, SM .
AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 77 (01) :112-119
[8]   Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer [J].
Fleischmann, C ;
Peto, J ;
Cheadle, J ;
Shah, B ;
Sampson, J ;
Houlston, RS .
INTERNATIONAL JOURNAL OF CANCER, 2004, 109 (04) :554-558
[9]   Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas [J].
Gismondi, V ;
Meta, M ;
Bonelli, L ;
Radice, P ;
Sala, P ;
Bertario, L ;
Viel, A ;
Fornasarig, M ;
Arrigoni, A ;
Gentile, M ;
De Leon, MP ;
Anselmi, L ;
Mareni, C ;
Bruzzi, P ;
Varesco, L .
INTERNATIONAL JOURNAL OF CANCER, 2004, 109 (05) :680-684
[10]  
Isidro Gloria, 2004, Hum Mutat, V24, P353, DOI 10.1002/humu.9282