Literature DB >> 30627969

Recent advances in Lynch syndrome.

Leah H Biller1, Sapna Syngal2,3,4, Matthew B Yurgelun5,6,7.   

Abstract

Lynch syndrome is one of the most common hereditary cancer predisposition syndromes and is associated with increased risks of colorectal and endometrial cancer, as well as multiple other cancer types. While the mechanism of mismatch repair deficiency and microsatellite instability and its role in Lynch-associated carcinogenesis has been known for some time, there have been significant advances recently in diagnostic testing and the understanding of the molecular pathogenesis of Lynch tumors. There is also an increased awareness that the clinical phenotype and cancer risk varies by specific mismatch repair mutation, which in turn has implications on surveillance strategies for patients. Even the treatment of Lynch-associated cancers has changed with the addition of immunotherapy for advanced disease. This progress report aims to review some of the many advances in epidemiology, molecular pathogenesis, diagnosis, clinical phenotype, cancer surveillance, treatment, and chemo- and immune-prevention strategies in the Lynch syndrome field over the past 5 years.

Entities:  

Keywords:  Cancer genetics; Hereditary cancer syndromes; Lynch syndrome

Mesh:

Substances:

Year:  2019        PMID: 30627969      PMCID: PMC6450737          DOI: 10.1007/s10689-018-00117-1

Source DB:  PubMed          Journal:  Fam Cancer        ISSN: 1389-9600            Impact factor:   2.375


  61 in total

1.  New EPCAM founder deletion in Polish population.

Authors:  D Dymerska; K Gołębiewska; M Kuświk; H Rudnicka; R J Scott; R Billings; A Pławski; P Boruń; M Siołek; B Kozak-Klonowska; M Szwiec; E Kilar; T Huzarski; T Byrski; J Lubiński; G Kurzawski
Journal:  Clin Genet       Date:  2017-08-03       Impact factor: 4.438

2.  Community Practice Implementation of a Self-administered Version of PREMM1,2,6 to Assess Risk for Lynch Syndrome.

Authors:  Daniel G Luba; James A DiSario; Colleen Rock; Devki Saraiya; Kelsey Moyes; Krystal Brown; Kristen Rushton; Maydeen M Ogara; Mona Raphael; Dayna Zimmerman; Kimmie Garrido; Evelyn Silguero; Jonathan Nelson; Matthew B Yurgelun; Fay Kastrinos; Richard J Wenstrup; Sapna Syngal
Journal:  Clin Gastroenterol Hepatol       Date:  2017-06-28       Impact factor: 11.382

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.  Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.

Authors:  Heather Hampel; Wendy Frankel; Jenny Panescu; Janet Lockman; Kaisa Sotamaa; Daniel Fix; Ilene Comeras; Jennifer La Jeunesse; Hidewaki Nakagawa; Judith A Westman; Thomas W Prior; Mark Clendenning; Pamela Penzone; Janet Lombardi; Patti Dunn; David E Cohn; Larry Copeland; Lynne Eaton; Jeffrey Fowler; George Lewandowski; Luis Vaccarello; Jeffrey Bell; Gary Reid; Albert de la Chapelle
Journal:  Cancer Res       Date:  2006-08-01       Impact factor: 12.701

5.  Defective mismatch repair as a predictive marker for lack of efficacy of fluorouracil-based adjuvant therapy in colon cancer.

Authors:  Daniel J Sargent; Silvia Marsoni; Genevieve Monges; Stephen N Thibodeau; Roberto Labianca; Stanley R Hamilton; Amy J French; Brian Kabat; Nathan R Foster; Valter Torri; Christine Ribic; Axel Grothey; Malcolm Moore; Alberto Zaniboni; Jean-Francois Seitz; Frank Sinicrope; Steven Gallinger
Journal:  J Clin Oncol       Date:  2010-05-24       Impact factor: 44.544

6.  Cancer risks for MLH1 and MSH2 mutation carriers.

Authors:  James G Dowty; Aung K Win; Daniel D Buchanan; Noralane M Lindor; Finlay A Macrae; Mark Clendenning; Yoland C Antill; Stephen N Thibodeau; Graham Casey; Steve Gallinger; Loic Le Marchand; Polly A Newcomb; Robert W Haile; Graeme P Young; Paul A James; Graham G Giles; Shanaka R Gunawardena; Barbara A Leggett; Michael Gattas; Alex Boussioutas; Dennis J Ahnen; John A Baron; Susan Parry; Jack Goldblatt; Joanne P Young; John L Hopper; Mark A Jenkins
Journal:  Hum Mutat       Date:  2013-03       Impact factor: 4.878

7.  Immune response against frameshift-induced neopeptides in HNPCC patients and healthy HNPCC mutation carriers.

Authors:  Yvette Schwitalle; Matthias Kloor; Susanne Eiermann; Michael Linnebacher; Peter Kienle; Hanns Peter Knaebel; Mirjam Tariverdian; Axel Benner; Magnus von Knebel Doeberitz
Journal:  Gastroenterology       Date:  2008-01-11       Impact factor: 22.682

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.  Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database.

Authors:  Pål Møller; Toni Seppälä; Inge Bernstein; Elke Holinski-Feder; Paola Sala; D Gareth Evans; Annika Lindblom; Finlay Macrae; Ignacio Blanco; Rolf Sijmons; Jacqueline Jeffries; Hans Vasen; John Burn; Sigve Nakken; Eivind Hovig; Einar Andreas Rødland; Kukatharmini Tharmaratnam; Wouter H de Vos Tot Nederveen Cappel; James Hill; Juul Wijnen; Kate Green; Fiona Lalloo; Lone Sunde; Miriam Mints; Lucio Bertario; Marta Pineda; Matilde Navarro; Monika Morak; Laura Renkonen-Sinisalo; Ian M Frayling; John-Paul Plazzer; Kirsi Pylvanainen; Julian R Sampson; Gabriel Capella; Jukka-Pekka Mecklin; Gabriela Möslein
Journal:  Gut       Date:  2015-12-09       Impact factor: 23.059

10.  Mutation spectrum in South American Lynch syndrome families.

Authors:  Mev Dominguez-Valentin; Mef Nilbert; Patrik Wernhoff; Francisco López-Köstner; Carlos Vaccaro; Carlos Sarroca; Edenir Ines Palmero; Alejandro Giraldo; Patricia Ashton-Prolla; Karin Alvarez; Alejandra Ferro; Florencia Neffa; Junea Caris; Dirce M Carraro; Benedito M Rossi
Journal:  Hered Cancer Clin Pract       Date:  2013-12-18       Impact factor: 2.857

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  19 in total

1.  Patients with unexplained mismatch repair deficiency are interested in updated genetic testing.

Authors:  Jessica Omark; Eduardo Vilar; Y Nancy You; Leslie Dunnington; Sarah Noblin; Blair Stevens; Maureen Mork
Journal:  Hered Cancer Clin Pract       Date:  2020-09-21       Impact factor: 2.857

Review 2.  The immune contexture and Immunoscore in cancer prognosis and therapeutic efficacy.

Authors:  Daniela Bruni; Helen K Angell; Jérôme Galon
Journal:  Nat Rev Cancer       Date:  2020-08-04       Impact factor: 60.716

Review 3.  Progress Report: New insights into the prevention of CRC by colonoscopic surveillance in Lynch syndrome.

Authors:  Hans F A Vasen
Journal:  Fam Cancer       Date:  2021-01-19       Impact factor: 2.375

Review 4.  Exploiting DNA Endonucleases to Advance Mechanisms of DNA Repair.

Authors:  Marlo K Thompson; Robert W Sobol; Aishwarya Prakash
Journal:  Biology (Basel)       Date:  2021-06-14

5.  Cancer risks in Lynch syndrome, Lynch-like syndrome, and familial colorectal cancer type X: a prospective cohort study.

Authors:  Karolin Bucksch; Silke Zachariae; Stefan Aretz; Reinhard Büttner; Elke Holinski-Feder; Stefanie Holzapfel; Robert Hüneburg; Matthias Kloor; Magnus von Knebel Doeberitz; Monika Morak; Gabriela Möslein; Jacob Nattermann; Claudia Perne; Nils Rahner; Wolff Schmiegel; Karsten Schulmann; Verena Steinke-Lange; Christian P Strassburg; Deepak B Vangala; Jürgen Weitz; Markus Loeffler; Christoph Engel
Journal:  BMC Cancer       Date:  2020-05-24       Impact factor: 4.430

6.  Identification of a novel pathogenic MLH1 mutation and recommended genetic screening strategy: An investigation of three Chinese Lynch syndrome pedigrees.

Authors:  Fan Li; Yunwei Xia; Guoguang Wang; Chaoyang Tang; Tian Zhan; Jian Shen; Jianping Zhang
Journal:  Mol Genet Genomic Med       Date:  2020-06-03       Impact factor: 2.183

7.  Sporadic and Lynch syndrome-associated mismatch repair-deficient brain tumors.

Authors:  Hyunhee Kim; Ka Young Lim; Jin Woo Park; Jeongwan Kang; Jae Kyung Won; Kwanghoon Lee; Yumi Shim; Chul-Kee Park; Seung-Ki Kim; Seung-Hong Choi; Tae Min Kim; Hongseok Yun; Sung-Hye Park
Journal:  Lab Invest       Date:  2021-11-30       Impact factor: 5.662

8.  Identification and management of Lynch syndrome in the Middle East and North African countries: outcome of a survey in 12 countries.

Authors:  Mohammad Sina; Zeinab Ghorbanoghli; Amal Abedrabbo; Fahd Al-Mulla; Rihab Ben Sghaier; Marie-Pierre Buisine; George Cortas; Ladan Goshayeshi; Andreas Hadjisavvas; Wail Hammoudeh; Waseem Hamoudi; Carol Jabari; Maria A Loizidou; Keivan Majidzadeh-A; Makia J Marafie; Gurbankhan Muslumov; Laila Rifai; Rania Abu Seir; Suzan M Talaat; Berrin Tunca; Hadia Ziada-Bouchaar; Mary E Velthuizen; Ala I Sharara; Aysel Ahadova; Demetra Georgiou; Hans F A Vasen
Journal:  Fam Cancer       Date:  2020-10-24       Impact factor: 2.375

Review 9.  Hereditary pancreatic cancer.

Authors:  Kodai Abe; Minoru Kitago; Yuko Kitagawa; Akira Hirasawa
Journal:  Int J Clin Oncol       Date:  2021-09-02       Impact factor: 3.402

10.  WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family.

Authors:  Mahnaz Norouzi; Mohammad Shafiei; Zeinab Abdollahi; Paniz Miar; Hamid Galehdari; Mohammad Hasan Emami; Mehrdad Zeinalian; Mohammad Amin Tabatabaiefar
Journal:  Front Oncol       Date:  2021-06-07       Impact factor: 6.244

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