Literature DB >> 33033905

Discordant DNA mismatch repair protein status between synchronous or metachronous gastrointestinal carcinomas: frequency, patterns, and molecular etiologies.

Monika Vyas1,2, Canan Firat1, Jaclyn F Hechtman1, Martin R Weiser3, Rona Yaeger4, Chad Vanderbilt1, Jamal K Benhamida1, Ajaratu Keshinro3, Liying Zhang5, Peter Ntiamoah1, Marco Gonzalez1, Rebecca Andrade1, Imane El Dika4, Arnold J Markowitz4, J Joshua Smith3, Julio Garcia-Aguilar3, Efsevia Vakiani1, David S Klimstra1, Zsofia K Stadler6, Jinru Shia7.   

Abstract

The widespread use of tumor DNA mismatch repair (MMR) protein immunohistochemistry in gastrointestinal tract (GIT) carcinomas has unveiled cases where the MMR protein status differs between synchronous/metachronous tumors from the same patients. This study aims at examining the frequency, patterns and molecular etiologies of such inter-tumoral MMR discordances. We analyzed a cohort of 2159 colorectal cancer (CRC) patients collected over a 5-year period and found that 1.3% of the patients (27/2159) had ≥ 2 primary CRCs, and 25.9% of the patients with ≥ 2 primary CRCs (7/27) exhibited inter-tumoral MMR discordance. We then combined the seven MMR-discordant CRC patients with three additional MMR-discordant GIT carcinoma patients and evaluated their discordant patterns and associated molecular abnormalities. The 10 patients consisted of 3 patients with Lynch syndrome (LS), 1 with polymerase proofreading-associated polyposis (PAPP), 1 with familial adenomatous polyposis (FAP), and 5 deemed to have no cancer disposing hereditary syndromes. Their MMR discordances were associated with the following etiologies: (1) PMS2-LS manifesting PMS2-deficient cancer at an old age when a co-incidental sporadic MMR-proficient cancer also occurred; (2) microsatellite instability-driven secondary somatic MSH6-inactivation occurring in only one-and not all-PMS2-LS associated MMR-deficient carcinomas; (3) "compound LS" with germline mutations in two MMR genes manifesting different tumors with deficiencies in different MMR proteins; (4) PAPP or FAP syndrome-associated MMR-proficient cancer co-occurring metachronously with a somatic MMR-deficient cancer; and (5) non-syndromic patients with sporadic MMR-proficient cancers co-occurring synchronously/metachronously with sporadic MMR-deficient cancers. Our study thus suggests that inter-tumoral MMR discordance is not uncommon among patients with multiple primary GIT carcinomas (25.9% in patients with ≥ 2 CRCs), and may be associated with widely varied molecular etiologies. Awareness of these patterns is essential in ensuring the most effective strategies in both LS detection and treatment decision-making. When selecting patients for immunotherapy, MMR testing should be performed on the tumor or tumors that are being treated.

Entities:  

Keywords:  Colorectal cancer; Gastrointestinal tract cancer; Hereditary cancer; Lynch syndrome; MMR IHC; Mismatch repair deficiency; Mutational testing

Mesh:

Substances:

Year:  2020        PMID: 33033905      PMCID: PMC8032798          DOI: 10.1007/s10689-020-00210-4

Source DB:  PubMed          Journal:  Fam Cancer        ISSN: 1389-9600            Impact factor:   2.446


  45 in total

1.  Clinical and molecular characteristics of hereditary non-polyposis colorectal cancer families in Southeast Asia.

Authors:  S-C Lee; J-Y Guo; R Lim; R Soo; E Koay; M Salto-Tellez; A Leong; B-C Goh
Journal:  Clin Genet       Date:  2005-08       Impact factor: 4.438

2.  Microsatellite instability and DNA mismatch repair protein deficiency in Lynch syndrome colorectal polyps.

Authors:  Matthew B Yurgelun; Ajay Goel; Jason L Hornick; Ananda Sen; Danielle Kim Turgeon; Mack T Ruffin; Norman E Marcon; John A Baron; Robert S Bresalier; Sapna Syngal; Dean E Brenner; C Richard Boland; Elena M Stoffel
Journal:  Cancer Prev Res (Phila)       Date:  2012-01-18

3.  Germline Genetic Features of Young Individuals With Colorectal Cancer.

Authors:  Elena M Stoffel; Erika Koeppe; Jessica Everett; Peter Ulintz; Mark Kiel; Jenae Osborne; Linford Williams; Kristen Hanson; Stephen B Gruber; Laura S Rozek
Journal:  Gastroenterology       Date:  2017-11-14       Impact factor: 22.682

4.  Distinct mutations in MLH1 and MSH2 genes in hereditary non-polyposis colorectal cancer (HNPCC) families from China.

Authors:  Wenqian Wei; Fangqi Liu; Lei Liu; Zuofeng Li; Xiaoyan Zhang; Fan Jiang; Qu Shi; Xiaoyan Zhou; Weiqi Sheng; Sanjun Cai; Xuan Li; Ye Xu; Peng Nan
Journal:  BMB Rep       Date:  2011-05       Impact factor: 4.778

5.  NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 2.2019.

Authors:  Samir Gupta; Dawn Provenzale; Xavier Llor; Amy L Halverson; William Grady; Daniel C Chung; Sigurdis Haraldsdottir; Arnold J Markowitz; Thomas P Slavin; Heather Hampel; Reid M Ness; Jennifer M Weiss; Dennis J Ahnen; Lee-May Chen; Gregory Cooper; Dayna S Early; Francis M Giardiello; Michael J Hall; Stanley R Hamilton; Priyanka Kanth; Jason B Klapman; Audrey J Lazenby; Patrick M Lynch; Robert J Mayer; June Mikkelson; Shajan Peter; Scott E Regenbogen; Mary A Dwyer; Ndiya Ogba
Journal:  J Natl Compr Canc Netw       Date:  2019-09-01       Impact factor: 11.908

6.  Clinicopathologic features of synchronous colorectal carcinoma: A distinct subset arising from multiple sessile serrated adenomas and associated with high levels of microsatellite instability and favorable prognosis.

Authors:  Huankai Hu; Daniel T Chang; Marina N Nikiforova; Shih-Fan Kuan; Reetesh K Pai
Journal:  Am J Surg Pathol       Date:  2013-11       Impact factor: 6.394

7.  Detection of DNA mismatch repair deficient crypts in random colonoscopic biopsies identifies Lynch syndrome patients.

Authors:  Randall E Brand; Beth Dudley; Eve Karloski; Rohit Das; Kimberly Fuhrer; Rish K Pai; Reetesh K Pai
Journal:  Fam Cancer       Date:  2020-04       Impact factor: 2.375

8.  Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer.

Authors:  Aung Ko Win; Mark A Jenkins; James G Dowty; Antonis C Antoniou; Andrew Lee; Graham G Giles; Daniel D Buchanan; Mark Clendenning; Christophe Rosty; Dennis J Ahnen; Stephen N Thibodeau; Graham Casey; Steven Gallinger; Loïc Le Marchand; Robert W Haile; John D Potter; Yingye Zheng; Noralane M Lindor; Polly A Newcomb; John L Hopper; Robert J MacInnis
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2016-10-31       Impact factor: 4.254

9.  Validation of a DNA methylation microarray for 850,000 CpG sites of the human genome enriched in enhancer sequences.

Authors:  Sebastian Moran; Carles Arribas; Manel Esteller
Journal:  Epigenomics       Date:  2015-12-17       Impact factor: 4.778

10.  Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.

Authors:  Mev Dominguez-Valentin; Julian R Sampson; Toni T Seppälä; Sanne W Ten Broeke; John-Paul Plazzer; Sigve Nakken; Christoph Engel; Stefan Aretz; Mark A Jenkins; Lone Sunde; Inge Bernstein; Gabriel Capella; Francesc Balaguer; Huw Thomas; D Gareth Evans; John Burn; Marc Greenblatt; Eivind Hovig; Wouter H de Vos Tot Nederveen Cappel; Rolf H Sijmons; Lucio Bertario; Maria Grazia Tibiletti; Giulia Martina Cavestro; Annika Lindblom; Adriana Della Valle; Francisco Lopez-Köstner; Nathan Gluck; Lior H Katz; Karl Heinimann; Carlos A Vaccaro; Reinhard Büttner; Heike Görgens; Elke Holinski-Feder; Monika Morak; Stefanie Holzapfel; Robert Hüneburg; Magnus von Knebel Doeberitz; Markus Loeffler; Nils Rahner; Hans K Schackert; Verena Steinke-Lange; Wolff Schmiegel; Deepak Vangala; Kirsi Pylvänäinen; Laura Renkonen-Sinisalo; John L Hopper; Aung Ko Win; Robert W Haile; Noralane M Lindor; Steven Gallinger; Loïc Le Marchand; Polly A Newcomb; Jane C Figueiredo; Stephen N Thibodeau; Karin Wadt; Christina Therkildsen; Henrik Okkels; Zohreh Ketabi; Leticia Moreira; Ariadna Sánchez; Miquel Serra-Burriel; Marta Pineda; Matilde Navarro; Ignacio Blanco; Kate Green; Fiona Lalloo; Emma J Crosbie; James Hill; Oliver G Denton; Ian M Frayling; Einar Andreas Rødland; Hans Vasen; Miriam Mints; Florencia Neffa; Patricia Esperon; Karin Alvarez; Revital Kariv; Guy Rosner; Tamara Alejandra Pinero; María Laura Gonzalez; Pablo Kalfayan; Douglas Tjandra; Ingrid M Winship; Finlay Macrae; Gabriela Möslein; Jukka-Pekka Mecklin; Maartje Nielsen; Pål Møller
Journal:  Genet Med       Date:  2019-07-24       Impact factor: 8.822

View more
  2 in total

1.  Primary Clonal Loss of Mismatch Repair Protein on Immunohistochemistry: A Pattern of Abnormality That Warrants Genetic Workup.

Authors:  Christine Orr; Chiyun Wang; Canan Firat; Louise C Connell; Margaret R Sheehan; Efsevia Vakiani; Zsofia K Stadler; Jinru Shia
Journal:  JCO Precis Oncol       Date:  2022-06

2.  Inoperable de novo metastatic colorectal cancer with primary tumour in situ: Evaluating discordant responses to upfront systemic therapy of the primary tumours and metastatic sites and complications arising from primary tumours (experiences from an Irish Cancer Centre).

Authors:  Ruba A Hamed; Sam Marks; Helen Mcelligott; Roshni Kalachand; Hawa Ibrahim; Said Atyani; Greg Korpanty; Nemer Osman
Journal:  Mol Clin Oncol       Date:  2021-12-21
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.