Literature DB >> 15528786

Identification of HNPCC by molecular analysis of colorectal and endometrial tumors.

H F A Vasen1, Y Hendriks, A E de Jong, M van Puijenbroek, C Tops, A H J T Bröcker-Vriends, J Th Wijnen, H Morreau.   

Abstract

Hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) is a dominantly inherited syndrome characterized by the development of colorectal cancer, endometrial cancer and other cancers and the presence of microsatellite instability (MSI) in tumors. The Bethesda guidelines have been proposed for the identification of families suspected of HNPCC that require further molecular analysis. We have evaluated the yield of MSI-analysis in a large series of Dutch families suspected of HNPCC. We also analysed whether the loss of mismatch repair (MMR) protein detected by immunohistochemistry (IHC) of colorectal cancer (CRC) and endometrial cancer correlated with the presence of MSI and/or a MMR gene mutation. The results showed that the Bethesda criteria with a few modifications are appropriate to identify families eligible for genetic testing. In addition, we found that MSI and IHC-analysis of CRC using antibodies against MLH1, MSH2, MSH6 and PMS2 proteins are equally effective for identifying carriers of the known MMR gene defects. However, as long as the role of other putative MMR genes in hereditary CRC has not been elucidated, IHC-analysis cannot completely replace MSI. For this reason, we prefer MSI-analysis as first step in families suspected of HNPCC. On the other hand, in families fulfilling the revised Amsterdam criteria in which the probability of detecting a mutation is relatively high, we would recommend IHC as first diagnostic step because the result might predict the specific underlying MMR gene mutation. MSI or IHC-analysis of endometrial cancer alone was found to be less sensitive compared with these tests performed in colorectal cancer. Therefore, probably the best approach in the analysis of this cancer is to perform both techniques. The identification of HNPCC is important as it makes it possible to target effective preventative measures. Our studies showed that MSI and IHC analysis of colorectal and endometrial cancer, are reliable cost-effective tools that can be used to identify patients with HNPCC.

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Year:  2004        PMID: 15528786      PMCID: PMC3839268          DOI: 10.1155/2004/391039

Source DB:  PubMed          Journal:  Dis Markers        ISSN: 0278-0240            Impact factor:   3.434


  13 in total

1.  Clinical Utility of Prospective Molecular Characterization in Advanced Endometrial Cancer.

Authors:  Tara E Soumerai; Mark T A Donoghue; Barry S Taylor; David M Hyman; Chaitanya Bandlamudi; Preethi Srinivasan; Matthew T Chang; Dmitriy Zamarin; Karen A Cadoo; Rachel N Grisham; Roisin E O'Cearbhaill; William P Tew; Jason A Konner; Martee L Hensley; Vicky Makker; Paul Sabbatini; David R Spriggs; Tiffany A Troso-Sandoval; Alexandra Snyder Charen; Claire Friedman; Mila Gorsky; Sarah J Schweber; Sumit Middha; Rajmohan Murali; Sarah Chiang; Kay J Park; Robert A Soslow; Marc Ladanyi; Bob T Li; Jennifer Mueller; Britta Weigelt; Ahmet Zehir; Michael F Berger; Nadeem R Abu-Rustum; Carol Aghajanian; Deborah F DeLair; David B Solit
Journal:  Clin Cancer Res       Date:  2018-08-01       Impact factor: 12.531

2.  Comparison of microsatellite status detection methods in colorectal carcinoma.

Authors:  Mei-Li Chen; Jie-Yu Chen; Jing Hu; Qian Chen; Li-Xia Yu; Bao-Rui Liu; Xiao-Ping Qian; Mi Yang
Journal:  Int J Clin Exp Pathol       Date:  2018-03-01

3.  Evidence of linkage to chromosomes 10p15.3-p15.1, 14q24.3-q31.1 and 9q33.3-q34.3 in non-syndromic colorectal cancer families.

Authors:  Ian W Saunders; Jason Ross; Finlay Macrae; Graeme P Young; Ignacio Blanco; Jesper Brohede; Glenn Brown; Diana Brookes; Trevor Lockett; Peter L Molloy; Victor Moreno; Gabriel Capella; Garry N Hannan
Journal:  Eur J Hum Genet       Date:  2011-08-10       Impact factor: 4.246

4.  Mismatch repair status and outcomes after adjuvant therapy in patients with surgically staged endometrial cancer.

Authors:  Kimberly E Resnick; Wendy L Frankel; Carl D Morrison; Jeffrey M Fowler; Larry J Copeland; Julie Stephens; Kenneth H Kim; David E Cohn
Journal:  Gynecol Oncol       Date:  2010-02-13       Impact factor: 5.482

5.  Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers.

Authors:  Wenche Sjursen; Bjørn Ivar Haukanes; Eli Marie Grindedal; Harald Aarset; Astrid Stormorken; Lars F Engebretsen; Christoffer Jonsrud; Inga Bjørnevoll; Per Arne Andresen; Sarah Ariansen; Liss Anne S Lavik; Bodil Gilde; Inger Marie Bowitz-Lothe; Lovise Maehle; Pål Møller
Journal:  J Med Genet       Date:  2010-06-28       Impact factor: 6.318

6.  Mismatch repair deficient-crypts in non-neoplastic colonic mucosa in Lynch syndrome: insights from an illustrative case.

Authors:  Jinru Shia; Zsofia K Stadler; Martin R Weiser; Efsevia Vakiani; Robin Mendelsohn; Arnold J Markowitz; Moshe Shike; C Richard Boland; David S Klimstra
Journal:  Fam Cancer       Date:  2015-03       Impact factor: 2.375

Review 7.  Current and emerging trends in Lynch syndrome identification in women with endometrial cancer.

Authors:  Kimberly E Resnick; Heather Hampel; Richard Fishel; David E Cohn
Journal:  Gynecol Oncol       Date:  2009-04-17       Impact factor: 5.482

8.  Immunohistochemistry versus microsatellite instability testing for screening colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome. Part I. The utility of immunohistochemistry.

Authors:  Jinru Shia
Journal:  J Mol Diagn       Date:  2008-06-13       Impact factor: 5.568

9.  Lynch syndrome among gynecologic oncology patients meeting Bethesda guidelines for screening.

Authors:  Christine S Walsh; Audra Blum; Ann Walts; Randa Alsabeh; Hang Tran; H Phillip Koeffler; Beth Y Karlan
Journal:  Gynecol Oncol       Date:  2010-01-19       Impact factor: 5.482

Review 10.  Hereditary non-polyposis colon cancer.

Authors:  L A Devlin; J H Price; P J Morrison
Journal:  Ulster Med J       Date:  2005-05
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