Corrigendum to: "Difficulties in recognizing families with Hereditary Non-polyposis Colorectal Carcinoma. Presentation of 4 families with proven mutation", [Eur J Surg Oncol 34 (2008) 1322-1327] (DOI:10.1016/j.ejso.2008.01.006);Difficulties in recognizing families with Hereditary Non-polyposis Colorectal Carcinoma. Presentation of 4 families with proven mutation

European Journal of Surgical Oncology

Volumn 34, Issue 12, 2008, Pages 1322-1327

  Tanyi, M ^a   Olasz, J ^b   Kamory E ^b   Csuka, O ^b   Tanyi, J L ^c   Ress, Z ^a   Damjanovich, L ^a  

^a UNIVERSITY OF DEBRECEN   (Hungary)

^b NATIONAL INSTITUTE OF ONCOLOGY   (Hungary)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

Bethesda criteria; Hereditary non polyposis colon cancer; hMLH1; hMSH2; Phenotypical variability

Indexed keywords

MICROSATELLITE DNA; PROTEIN MLH1; PROTEIN MSH2;

ADULT; ARTICLE; CASE REPORT; COLORECTAL CANCER; DNA SEQUENCE; FAMILIAL CANCER; FAMILY HISTORY; FEMALE; GENE MUTATION; HISTOLOGY; HUMAN; IMMUNOHISTOCHEMISTRY; MALE; PEDIGREE ANALYSIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 54849437576     PISSN: 07487983     EISSN: 15322157     Source Type: Journal    
DOI: 10.1016/j.ejso.2009.02.002     Document Type: Erratum

References (19)

1. Lawes D.A., Sengupta S.B., Boulos P.B., et al. Pathogenesis and clinical management of hereditary non-polyposis colorectal cancer. Br J Surg 89 (2002) 1357-1369
2. Lynch H.T., Schuelke G.S., Kimberling W.J., et al. Hereditary nonpolyposis colorectal cancer (Lynch syndrome I and II). II. Biomarker studies. Cancer 56 (1985) 939-951
3. Lynch H.T., Lanspa S., Smyrk T., Boman B., Watson P., and Lynch J. Hereditary nonpolyposis colorectal cancer (Lynch syndromes I & II). Genetics, pathology, natural history, and cancer control, part I. Cancer Genet Cytogenet 5 (1991) 143-160
4. Debniak T., Kurzawski G., Gorski B., et al. Value of pedigree/clinical data, immunohistochemistry and microsatellite instability analyses in reducing the cost of determining hMLH1 and hMSH2 gene mutations is patients with colorectal cancer. Eur J Cancer 36 (2000) 49-54
5. Jass J.R. Hereditary non-polyposis colorectal cancer: the rise and fall of a confusing term. World J Gastroenterol 12 31 (2006) 4943-4950
6. Boland C.R., Thibodeau S.N., Hamilton S.R., et al. A National Cancer Institute workshop on microsatellite instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res 58 (1998) 5248-5257
7. Beck N.E., Tomlinson I.P.M., Homfray T., et al. Use of SSCP analysis to identify germline mutations in HNPCC families fulfilling the Amsterdam criteria. Hum Genet 99 (1997) 219-224
8. Yanagisawa Y., Akiyama Y., Iida S., et al. Methylation of the hMLH1 promoter in familial gastric cancer with microsatellite instability. Int J Cancer 85 (2000) 50-53
9. The Human Gene Mutation Database Cardiff. http://archive.uwcm.ac.uk/uwcm/mg/searc/203983.htlm.
10. International Society for Gastrointestinal Hereditary Tumors. http://www.insight-group.org.
11. Tanyi M., Olasz J., Lukács G., et al. Pedigree and genetic analysis of a novel mutation carrier patient suffering from hereditary nonpolyposis colorectal cancer. World J Gastroenterol 12 8 (2006) 1192-1197
12. Kámory E., Tanyi M., Kolacsek O., et al. Two germline alterations in mismatch repair genes found in a HNPCC patient with poor family history. Pathol Oncol Res 12 4 (2006) 228-233
13. Kurzawski G., Safranow K., Suchy J., Chlubek D., Scott R.J., and Lubinski J. Mutation analysis of MLH1 and MSH2 genes performed by denaturing high-performance liquid chromatography. J Biochem Biophys Methods 51 (2002) 89-100
14. Lynch H.T., Riley B.D., Weismann S., et al. Hereditary nonpolyposis colorectal carcinoma (HNPCC) and HNPCC-like families: problems in diagnosis, surveillance, and management. Cancer 100 (2003) 53-64
15. Samowitz W.S., Curtin K., Lin H.H., et al. The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer. Gastroenterology 121 (2001) 830-838
16. National Institute of Environmental Health Sciences Genome Project, NIEHS SNPs. http://egp.gs.washington.edu/M.htlm.
17. Hutter P., Couturier A., Membrez V., et al. Excess of hMLH1 germline mutations in Swiss families with hereditary non-polyposis colorectal cancer. Int J Cancer 78 (1998) 80-84
18. Cederquist K., Emanuelsson M., Goransson I., et al. Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: a population-based study in northern Sweden. Int J Cancer 109 (2004) 370-376
19. Kurzawski G., Suchy J., Kladny J., et al. Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic States. [abstract]. J Med Genet 39 (2002) e65