Microsatellite Instability Use in Mismatch Repair Gene Sequence Variant Classification

被引:6
作者
Thompson, Bryony A. [1 ,2 ]
Spurdle, Amanda B. [1 ]
机构
[1] QIMR Berghofer Med Res Inst, Genet & Computat Biol Dept, Brisbane, Qld 4006, Australia
[2] Univ Utah, Huntsman Canc Inst, Dept Oncol Sci, Salt Lake City, UT 84112 USA
关键词
lynch syndrome; variants of uncertain significance; mismatch repair; variant classification; multifactorial likelihood model; NONPOLYPOSIS COLORECTAL-CANCER; UNKNOWN CLINICAL-SIGNIFICANCE; LYNCH-SYNDROME; ENDOMETRIAL CANCER; COLON-CANCER; MISSENSE SUBSTITUTIONS; TUMOR CHARACTERISTICS; PROMOTER METHYLATION; PATHOLOGY FEATURES; MUTATION CARRIERS;
D O I
10.3390/genes6020150
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Inherited mutations in the DNA mismatch repair genes (MMR) can cause MMR deficiency and increased susceptibility to colorectal and endometrial cancer. Microsatellite instability (MSI) is the defining molecular signature of MMR deficiency. The clinical classification of identified MMR gene sequence variants has a direct impact on the management of patients and their families. For a significant proportion of cases sequence variants of uncertain clinical significance (also known as unclassified variants) are identified, constituting a challenge for genetic counselling and clinical management of families. The effect on protein function of these variants is difficult to interpret. The presence or absence of MSI in tumours can aid in determining the pathogenicity of associated unclassified MMR gene variants. However, there are some considerations that need to be taken into account when using MSI for variant interpretation. The use of MSI and other tumour characteristics in MMR gene sequence variant classification will be explored in this review.
引用
收藏
页码:150 / 162
页数:13
相关论文
共 82 条
[1]   CLUES TO THE PATHOGENESIS OF FAMILIAL COLORECTAL-CANCER [J].
AALTONEN, LA ;
PELTOMAKI, P ;
LEACH, FS ;
SISTONEN, P ;
PYLKKANEN, L ;
MECKLIN, JP ;
JARVINEN, H ;
POWELL, SM ;
JEN, J ;
HAMILTON, SR ;
PETERSEN, GM ;
KINZLER, KW ;
VOGELSTEIN, B ;
DELACHAPELLE, A .
SCIENCE, 1993, 260 (5109) :812-816
[2]   Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease [J].
Aaltonen, LA ;
Salovaara, R ;
Kristo, P ;
Canzian, F ;
Hemminki, A ;
Peltomäki, P ;
Chadwick, RB ;
Kääriäinen, H ;
Eskelinen, M ;
Järvinen, H ;
Mecklin, JP ;
de la Chapelle, A ;
Percesepe, A ;
Ahtola, H ;
Härkönen, N ;
Julkunen, R ;
Kangas, E ;
Ojala, S ;
Tulikoura, J ;
ValKamo, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (21) :1481-1487
[3]   hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6 [J].
Acharya, S ;
Wilson, T ;
Gradia, S ;
Kane, MF ;
Guerrette, S ;
Marsischky, GT ;
Kolodner, R ;
Fishel, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (24) :13629-13634
[4]   Estimating cancer risk in HNPCC by the GRL method [J].
Alarcon, Flora ;
Lasset, Christine ;
Carayol, Jerome ;
Bonadona, Valerie ;
Perdry, Herve ;
Desseigne, Francoise ;
Wang, Qing ;
Bonaiti-Pellie, Catherine .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2007, 15 (08) :831-836
[5]  
[Anonymous], APPL IMMUNOHISTOCHEM
[6]  
[Anonymous], CANCER
[7]   Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer [J].
Barnetson, Rebecca A. ;
Cartwright, Nicola ;
van Vliet, Annelot ;
Haq, Naila ;
Drew, Kate ;
Farrington, Susan ;
Williams, Nicola ;
Warner, Jon ;
Campbell, Harry ;
Porteous, Mary E. ;
Dunlop, Malcolm G. .
HUMAN MUTATION, 2008, 29 (03) :367-374
[8]   Cancer risk in Lynch Syndrome [J].
Barrow, Emma ;
Hill, James ;
Evans, D. Gareth .
FAMILIAL CANCER, 2013, 12 (02) :229-240
[9]  
Boland CR, 2010, GASTROENTEROLOGY, V138, P2073, DOI [10.1053/j.gastro.2009.12.064, 10.1053/j.gastro.2010.04.024]
[10]  
Boland CR, 1998, CANCER RES, V58, P5248