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Originally published as JCO Early Release 10.1200/JCO.2004.02.033 on October 13 2004 © 2004 American Society of Clinical Oncology. Lower Incidence of Colorectal Cancer and Later Age of Disease Onset in 27 Families With Pathogenic MSH6 Germline Mutations Compared With Families With MLH1 or MSH2 Mutations: The German Hereditary Nonpolyposis Colorectal Cancer ConsortiumFrom the Department of Surgical Research, Dresden University of Technology, Dresden; Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig; Department of Medical Genetics, University of Munich, Munich; Institute of Human Genetics, University Hospital Bonn, Bonn; Department of Surgery, Heinrich-Heine-University, Düsseldorf, Düsseldorf; Department of Medicine, Knappschaftskrankenhaus, Ruhr University Bochum, Bochum; Department of Pathology, Division of Molecular Pathology, University of Heidelberg, Heidelberg; Institute of Pathology, Klinikum Kassel, Kassel, Germany Address reprint requests to Jens Plaschke, PhD, Department of Surgical Research, Universitätsklinikum Carl Gustav Carus, Dresden University of Technology, Fetscherstrasse 74, 01307 Dresden, Germany; e-mail: plaschke{at}rcs.urz.tu-dresden.de
PURPOSE: The aim of the study was the analysis of the involvement and phenotypic manifestations of MSH6 germline mutations in families suspected of hereditary nonpolyposis colorectal cancer (HNPCC). PATIENTS AND METHODS: Patients were preselected among 706 families by microsatellite instability, immunohistochemistry, and/or exclusion of MLH1 or MSH2 mutations and were subjected to MSH6 mutation analysis. Clinical and molecular data of MSH6 mutation families were compared with data from families with MLH1 and MSH2 mutations. RESULTS: We identified 27 families with 24 different pathogenic MSH6 germline mutations, representing 3.8% of the total of the families, and 14.7% of all families with DNA mismatch repair (MMR) gene mutations (n = 183). The median age of onset of colorectal cancer in putative mutation carriers was 10 years higher for MSH6 (54 years; 95% CI, 51 to 56) compared with MLH1 and MSH2 (44 years; 95% CI, 43 to 45; log-rank test, P = .0038). Relative to other malignant tumors, colorectal cancer was less frequent in MSH6 families compared with MLH1 and MSH2 families (Fisher's exact test, P < .001). In contrast, the frequency of non–HNPCC-associated tumors was increased (Fisher's exact test, P < .001). CONCLUSION: Later age of disease onset and lower incidence of colorectal cancer may contribute to a lower proportion of identified MSH6 mutations in families suspected of HNPCC. However, in approximately half of these families, at least one patient developed colorectal or endometrial cancer in the fourth decade of life. Therefore, a surveillance program as stringent as that for families with MLH1 or MSH2 mutations is recommended.
Hereditary nonpolyposis colorectal cancer (HNPCC; MIM 114500) is a highly penetrant, autosomal dominant cancer-susceptibility syndrome. Affected individuals are at high risk for developing colorectal and endometrial cancer. In addition, there is an excess of cancers of ovary, stomach, small bowel, pancreas, hepatobiliary tract, brain and upper uroepithelial tract.1 A hallmark of most of these malignancies is the contraction/expansion of simple sequence motifs,2-4 termed microsatellite instability (MSI) or microsatellite mutator phenotype. Disease-causing germline mutations in the mismatch repair genes MLH1 (MIM No. 120436; GenBank accession: AH003234), MSH2 (MIM No. 120435; GenBank accession: AH003235), PMS2 (MIM No. 600259; GenBank accession: U13696), and MSH6 (MIM No. 600678; GenBank accession: AH005068) have been described.5 The majority of germline mutations in HNPCC and suspected HNPCC cases have been identified in MLH1 and MSH2.5,6 A surveillance program should be offered to family members with pathogenic DNA mismatch repair (MMR) gene mutations or high clinical suspicion of HNPCC. People should undergo colonoscopy every 1 to 2 years beginning at age 20 to 25 years, or 10 years earlier than the youngest age of colon cancer diagnosis in the family.7 For extracolonic manifestations, the International Collaborative Group on HNPCC (ICG-HNPCC) recommends gynecologic examinations for women, including transvaginal ultrasonography and measurement of CA-125 every 1 to 2 years beginning at age 30 to 35 years. Surveillance for other extracolonic tumors should be tailored to the spectrum of malignancies observed in the family. Therefore, if at least one family member is affected with stomach cancer or cancer of the urinary tract, gastroscopy or sonography and urine cytology every 1 to 2 years starting at age 30 to 35 should be offered, respectively (http://www.nfdht.nl/guidelines.htm). Whether prophylactic surgery should be considered at the time of first diagnosis of colorectal cancer in HNPCC patients is under debate.8-10 As an individualized decision after counseling, prophylactic surgery represents an option to some HNPCC patients.11
At present, data from the HNPCC mutation database (http://www.nfdht.nl) and from the literature indicate that MSH6 mutations may account for 10% to 15% of all HNPCC germline mutations. Studies on patients with familial non-HNPCC colorectal carcinomas12 and on unselected patients with endometrial carcinomas13 suggest that approximately 1% to 2% of these cancers may be caused by MSH6 germline mutations. A predominance of instability at mononucleotide repeats in MSH6-deficient tumors has been reported,14-17 which is in accordance with the recognition of base-base mispairs and insertion/deletion loops (IDLs) of single bases by the MutS The risk of developing colorectal or endometrial cancer has been described as slightly higher in families with MSH2 mutations compared with families with MLH1 mutations, without reaching statistical significance.21 In contrast, MSH6 germline mutations were reported in families with a later age of tumor onset and a higher incidence of endometrial cancers when compared with families with MSH2 germline mutations.16 The average age of disease onset has been shown as higher in MSH6 mutation carriers than in MLH1 and MSH2 mutation carriers, which might reflect a lower penetrance of MSH6 mutations.15,20 Detailed analyses of phenotypic manifestations associated with hereditary MSH6 defects has been hampered by the limited number of identified germline mutations. Here we report on the molecular and clinical data of 27 families with pathogenic MSH6 mutations demonstrating a lower incidence of colorectal cancer and later age of disease onset compared with families with MLH1 or MSH2 mutations.
Patients were recruited from the German HNPCC registry established in 1999. The main goal of the registry is to support surveillance in families suspected of HNPCC. Patients are referred to the registry nationwide based on the Amsterdam I and II criteria22 without age restriction, and the Bethesda guidelines for the identification of patients with HNPCC.23 These criteria include (1) patients of families with at least three members affected with histologically verified colorectal, endometrial, small bowel, renal pelvis, or ureter cancer, in which one affected member is a first-degree relative of the other two and at least two generations are affected; (2) individuals with two HNPCC-associated cancers (colon, rectum, endometrium, ovary, stomach, biliary duct, small-bowel, ureter); (3) individuals with colorectal cancer and a first-degree relative with colorectal cancer and/or HNPCC-related extracolonic cancer and/or a colorectal adenoma in which one of the cancers was diagnosed prior to age 45 years, and the adenoma was diagnosed prior to age 40 years; (4) individuals with colorectal cancer or endometrial cancer diagnosed before age 45 years; (5) individuals with adenoma diagnosed before age 40 years; and (6) individuals with at least one relative fulfilling one of criteria 1 through 5. Familial adenomatous polyposis coli is excluded. Pedigree information is traced by clinical geneticists. A total of 706 families had been registered by January 2003. Whenever available, tumors samples have been analyzed for MSI and MLH1 and MSH2 protein expression. From this cohort, we selected candidates for MSH6 germline mutations using the following criteria: (1) the patients had developed tumors that were either of low or high MSI (MSI-L or MSI-H, respectively), and (2) MLH1 and MSH2 were expressed in the tumor cells. Tumor samples from selected patients were studied for MSH6 expression using immunohistochemistry techniques. In addition, patients were included in the study if no MLH1 or MSH2 germline mutation had been identified and no information on MSI and protein expression was available. Written informed consent was obtained from all patients investigated. Information on MSI was obtained from the application of the National Cancer Institute/ICG-HNPCC (NCI/ICG-HNPCC) reference marker panel for the evaluation of MSI in colorectal cancer (BAT25, BAT26, D2S123, D5S346, D17S250)24 for most tumors. If only one marker scored as instable, we applied a second marker panel (BAT40, D3S1619, D10S197, D18S58, MycL). In addition, other markers have been used as previously described.25,26 Tumors were classified as MSI-H or MSI-L if at least 30% or less than 30% of the markers showed instability, respectively. Immunohistochemical staining was performed on 5-µm-thick formalin-fixed, paraffin-embedded tumor sections using a mouse monoclonal primary antibody against MSH6 (clone 44; Transduction Laboratories, Lexington, UK; 250 µg/mL, 1:50) as described previously.17 Loss of expression in the tumor cells was considered solely when there was normal nuclear staining in adjacent non-neoplastic cells, which served as internal controls. Mutation analysis was performed on all exons of MSH6, including flanking intronic regions from genomic DNA isolated from peripheral blood lymphocytes either by denaturing high-performance liquid chromatography screening and subsequent sequencing or by direct sequencing as previously described.26,27 The functional effect of a splice donor site mutation was analyzed by reverse transcriptase-polymerase chain reaction with exonic primers after mRNA isolation from peripheral blood and reverse transcription applying the Quick-Prep Micro mRNA Purification Kit (Amersham Biosciences, Freiburg, Germany) and the First-Strand cDNA Synthesis Kit (Amersham Biosciences), respectively. To test whether two MSH6 mutations occurring in one of the patients were located on the same allele, a 7-kb fragment covering both mutations was amplified, cloned with the TOPO TA Cloning Kit (Invitrogen, Karlsruhe, Germany), and sequenced from both ends. Sequence information on the applied primers is available on request.
Statistical analyses were performed applying the
We identified 24 different germline mutations in MSH6 considered to be pathogenic in 27 families (Table 1). The mutations comprised eight nonsense mutations, seven small insertions, seven small deletions, and two genomic rearrangements. There was little redundancy, and only one mutation was found twice and three times, respectively. Mutations were distributed equally alongside the gene, with the exception of six (24%) of the 25 small mutations (not considering the two genomic rearrangements) that occurred in exon 5, representing only 6.5% of the coding region (six mutations in 266 bp coding region v 19 mutations in 3,817 bp;  2 P < .001).
MSI analysis of 24 available tumors from patients harboring pathogenic mutations revealed 19 (79%) MSI-H tumors, four (17%) MSI-L tumors, and one microsatellite-stable (MSS) tumor (Table 2). The patient with the MSS tumor (BN5, endometrial carcinoma) was included in the MSH6 analysis since the tumor showed loss of MSH6 expression, and the mother was also affected by a MSI-L endometrial carcinoma at age 57 years. Notably, one colon tumor (LM2) was MSI-L without showing instability in any of the five markers of the NCI/ICG-HNPCC marker panel. Mononucleotide repeats were more often affected by instability (51 [77.3%] of 66) when compared with di- and tetranucleotide repeats (34 [36.6%] of 93; 2 P < .001). Immunohistochemical analysis revealed loss of MSH6 expression in 18 tumors, whereas three tumors expressed the protein. There was a statistical difference in the number of families fulfilling Amsterdam and Bethesda criteria between MSH6 and MLH1/MSH2 carriers (Fisher's exact test, P = .017). A lower proportion of families carrying MSH6 mutations fulfilled the Amsterdam criteria without age restriction (48.1%) than those with MLH1 or MSH2 mutations (60.3%), while a higher proportion of the MSH6 families (25.9% v 9.0% of MLH1 and MSH2 families) met Bethesda criterion 4 (one family member with colorectal or endometrial cancer before age 45 years). Four families fulfilled the Amsterdam criteria by anamnestic data but not by age restriction. The disease history of families with MSH6 mutations is detailed in Table 1.
In addition to the 27 pathogenic mutations, five missense mutations with unknown pathogenicity were identified in MSH6 (Table 1). One of these mutations (E619D) was located on the same allele as a 4-bp deletion affecting the splice donor site of intron 7, resulting in skipping of exon 7 from the transcript. While the 4-bp deletion was a de novo mutation, the missense mutation was inherited from the patient's father. This patient (DD4) was affected with colon cancer at age 34 years and had no history of HNPCC-associated tumors in his family. The anamnestic data of patient BN1 was similar, with colon cancer at age 31 and lack of HNPCC-associated cancers among his relatives; however, in this family, the MSH6 mutation was inherited from the mother, who was affected with breast cancer at age 66 years. Among the 396 enrolled members of families with pathogenic MSH6 mutations, 115 (29.0%) were affected by a malignant disease. This frequency was lower than in families with MLH1 or MSH2 mutations (37.5%; Table 3). The main tumor entity of the HNPCC syndrome, colorectal cancer, was statistically less frequent among all tumors in families with MSH6 mutations (42.4%) compared with those with MLH1 or MSH2 mutations (65.5%; Table 4). Such a difference was not observed for other HNPCC-associated cancers. In contrast, the frequency of non–HNPCC-associated tumors was increased, as 46 (31.9%) of 144 primary tumors reported in MSH6 families were not of an HNPCC-associated type, compared with 131 (15.3%) of 859 tumors in MLH1 and MSH2 families (Fisher's exact test, P < .001). These tumors included breast, lung, and prostate cancer, and leukemia (Table 5). The median age of onset of colorectal cancer in putative mutation carriers was 10 years higher for MSH6 (54 years; 95% CI, 51 to 56 years) compared with MLH1 and MSH2 (44 years; 95% CI, 43 to 45 years). The median age of onset of any tumor was 8 years higher for MSH6 (51 years; 95% CI, 48 to 54 years) compared with MLH1 and MSH2 (43 years; 95% CI, 42 to 44 years). Accordingly, the cumulative risk by age to develop colorectal cancer or to develop any tumor was statistically lower for putative MSH6 mutation carriers compared with putative MLH1 and MSH2 mutation carriers, whereas no difference was obtained for non–colorectal HNPCC-associated cancers (Figs 1A to C).
In this study, molecular and clinical characteristics of 27 families with pathogenic MSH6 germline mutations are presented and compared with data from families with MLH1 or MSH2 mutations. MSH6 mutations were found in 3.8% of all HNPCC-suspected families (27 of 706 families), representing 14.7% of all 183 pathogenic germline mutations identified in the three MMR genes (MLH1, MSH2, and MSH6) in this cohort. These frequencies were somewhat higher, although not statistically different, when compared with the 2.4% in HNPCC-suspected families (two mutations in 84 families) reported by Peterlongo et al28 and to the 12% of all MMR gene mutations (10 of 83 mutations) reported by Wijnen et al,16 respectively. The age of disease onset in members of families with MSH6 mutations was increased compared with those of families with MLH1 and MSH2 mutations. The median and the mean age of onset of colorectal cancer in putative mutation carriers (both 54 years) were similar to the mean age (55 years) reported for a large Dutch family with a MSH6 germline mutation.15 Whether the lower cumulative risk of disease onset by age results in a lower lifetime risk in developing cancer in MSH6 mutation carriers cannot be concluded from our data because of the limited time of surveillance. Notably, a substantial fraction of patients with MSH6 mutations who did not fulfill any of the Bethesda guidelines for HNPCC has been identified in several population-based approaches,12,13,17,29 suggesting an even higher difference in the cumulative risk by age of disease onset between MSH6 mutation carriers and MLH1 and MSH2 mutation carriers, if all mutations in the general population were considered. Almost two-thirds (17 of 27) of the families with MSH6 mutations would not have been identified by application of the strict Amsterdam I and II criteria (with restriction for age of onset of at least one HNPCC-associated cancer before age 50 years). Moreover, no HNPCC-associated cancer was diagnosed before age 45 years—the limit for Bethesda criteria 3 and 4, in 10 of the families. Therefore, a relaxed age restriction in the application of clinical criteria may contribute to a more complete enrollment of families with MSH6 mutations. Although the clinicians in North America do not currently have MSH6 sequence analysis from all commercial laboratories providing gene-sequencing service for hereditary cancer syndromes, our data recommend the inclusion of this gene into the molecular diagnostics repertoire of HNPCC. Notwithstanding that patients with pathogenic MSH6 mutations were less frequently affected by multiple primary tumors, four of the index patients developed multiple primary colorectal cancers. These patients underwent standard oncological resections on all primary tumors, except for patient LM2, who underwent colonoscopic polypectomy of two synchronous colon carcinomas and refused the recommended subsequent standard resection. The secondary tumors were not related to ultimate mortality of these patients. Therefore, there is no indication that based on the recognition of an MSH6 germline mutation, an extended, prophylactic surgery would have been useful in these cases. Twenty-four of the 27 mutations were different and almost equally distributed throughout the MSH6 gene, except for a relative accumulation in exon 5 according to its proportion of the entire coding region. Four of the six mutations in exon 5 resulted from frameshift mutations affecting the (C)8 tract. The 1-bp insertion in this tract was first reported in Korean patients30 and is listed in the HNPCC database for an Australian patient. We have identified this mutation in an additional patient who was not included in this study due to failure to fulfill any of the criteria for patient selection (colon cancer at age 47 years). Therefore, this mutation accounts for approximately 10% of all MSH6 germline mutations reported thus far, and constitutes, with the c.651_652insT, a founder mutation in the population of the Netherlands,16 one of the two most common MSH6 germline mutations. The frequent occurrence of frameshift mutations at this site might be explained by the susceptibility of homopolymeric sequences to strand slippage errors, which is also emphasized by frequent somatic mutations of this C(8) tract in MMR-deficient tumors.31 Moreover, these findings are similar to those of MLH1 in our cohort, where the most frequent mutation was the insertion of a cytosine residue to the (C)6 tract in exon 13 (data not shown). The majority of tumors showed both MSI and loss of MSH6 expression, whereas few patients with identified MSH6 mutations were included in the analysis by having developed an MSI tumor expressing MSH6 (three patients) or an MSS tumor with loss of MSH6 expression (one patient). Therefore, neither MSI analyses nor protein expression analyses were able to select all patients with MSH6 mutations, which is similar to results reported by Wu et al19 and Berends et al.20 Moreover, our results do not exclude the possibility that even the combination of both methods might not identify all patients with MSH6 mutations. The retained expression of MSH6 in some tumors may be explained by somatic mutations of the second allele impairing protein function but not expression. The MSI phenotype is, on average, less pronounced in MSH6-deficient tumors when compared with MLH1- or MSH2-deficient tumors, and mononucleotide repeat markers are more frequently affected than dinucleotide repeat markers. Therefore, the question remains as to whether the use of a larger number of long mononucleotide repeats would increase the sensitivity in the selection of patients with MSH6 germline mutations, regardless of tumor origin. The frequency of colorectal cancer, the main tumor type in HNPCC syndrome, was lower in MSH6 families compared with MLH1 and MSH2 families, whereas non–HNPCC-associated tumors were statistically more frequent. The basis of this shift in tumor spectrum is not known. One explanation may be that the extended strand slippage errors at coding microsatellites (namely, frameshift mutations of the [A]10 tract of TGFßRII), which are found in 80% of colorectal cancers of the MSI-H phenotype,32 may favor the development of colorectal cancer in individuals carrying MLH1 and MSH2 mutations. In contrast, the decreased frequency of frameshift mutations and similar or even increased levels of point mutations associated with MSH6-deficiency, as compared with MLH1- or MSH2-deficiency,18,33 may explain the slower tumor development and reduced prevalence of colorectal cancer. It is not clear why MSH6 is less frequently affected by germline mutations when compared with MLH1 and MSH2, since MSH6 has approximately a 50% larger coding region. Our findings suggest that MSH6 germline mutations may become less frequently evident than MLH1 or MSH2 mutations when the Bethesda criteria are applied because of a later age of tumor onset and a reduced frequency of colorectal cancer. Furthermore, the lower frequency of colorectal cancer along with the increased frequency of non–HNPCC-associated tumors in families with MSH6 mutations raises the question of whether some families with tumor histories not suspected of HNPCC are associated with MSH6 germline mutations. The partially retained MMR capacity due to mutated MSH6, compared with an incapacity in mutated MSH2,18,34 may be responsible for the later age of tumor onset in patients with MSH6 germline mutations. Nonetheless, in approximately half of the families with MSH6 germline mutations, at least one member developed colorectal or endometrial cancer in the fourth decade of life. This suggests a high variability regarding the penetrance by age of MSH6 germline mutations, which might be based on additional genetic and/or environmental factors. Therefore, a surveillance program as stringent as that for families with MLH1 or MSH2 mutations is recommended.
The German HNPCC-Consortium consists of the following centers (in alphabetic order): clinical centers in Bochum (in addition to author: F. Brasch, J.T. Epplen, S. Hahn, E. Kunstmann, C. Pox, W. Schmiegel, J. Willert), Bonn (in addition to authors: R. Büttner, W. Friedl, A. Hirner, C. Lamberti, M. Mathiak, P. Propping, T. Sauerbruch), Düsseldorf (in addition to author: T.O. Goecke, A. Hansmann, S. Höwer, C. Poremba, A. Unger, T. Vogel, C. Wieland), Dresden (in addition to authors: D.E. Aust, F. Balck, G. Baretton, R. Höhl, F.R. Kreuz, S.R. Pistorius, H.D. Saeger), Heidelberg (in addition to authors: A. Buckowitz, M. Keller, P. Kienle, M. Kloor, H.P. Knäbel, U. Mazitschek, M. Taraverdian), München/Regensburg (in addition to author: W. Dietmaier, M. Gross, R. Kopp, P. Lohse, M. Muders, Y. Müller-Koch, H. Vogelsang), center for reference pathology Kassel (in addition to author: T. Brodegger) and center for documentation and biometry in Leipzig (in addition to authors: J. Forberg, M. Herold).
The authors indicated no potential conflicts of interest.
We thank M. Reichmann and A. Rudek for excellent technical assistance. This work was supported by the Verbundprojekt "Familiärer Darmkrebs" of the Deutsche Krebshilfe (German Cancer Aid).
Supported by the Verbundprojekt "Familiärer Darmkrebs" of the Deutsche Krebshilfe (DKH, German Cancer Aid). Authors' disclosures of potential conflicts of interest are found at the end of this article.
1. Lynch HT, de la Chapelle A: Hereditary colorectal cancer. N Engl J Med 348:919-932, 2003
2. Aaltonen LA, Peltomaki P, Leach FS, et al: Clues to the pathogenesis of familial colorectal cancer. Science 260:812-816, 1993 3. Ionov Y, Peinado MA, Malkhosyan S, et al: Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis. Nature 363:558-561, 1993[CrossRef][Medline]
4. Thibodeau SN, Bren G, Schaid D: Microsatellite instability in cancer of the proximal colon. Science 260:816-819, 1993
5. Peltomaki P: Deficient DNA mismatch repair: A common etiologic factor for colon cancer. Hum Mol Genet 10:735-740, 2001 6. Liu B, Parsons R, Papadopoulos N, et al: Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients. Nat Med 2:169-174, 1996[CrossRef][Medline] 7. Winawer S, Fletcher R, Rex D, et al: Colorectal cancer screening and surveillance: Clinical guidelines and rationale—Update based on new evidence. Gastroenterology 124:544-560, 2003[CrossRef][Medline]
8. Burke W, Petersen G, Lynch P, et al: Recommendations for follow-up care of individuals with an inherited predisposition to cancer, I: Hereditary nonpolyposis colon cancer Cancer Genetics Studies Consortium. JAMA 277:915-919, 1997 9. Lynch HT, Lynch JF, Fitzgibbons R Jr: Role of prophylactic colectomy in Lynch syndrome. Clin Colorectal Cancer 3:99-101, 2003[Medline] 10. Scaife CL, Rodriguez-Bigas MA: Lynch syndrome: Implications for the surgeon. Clin Colorectal Cancer 3:92-98, 2003[Medline] 11. Pistorius SR, Nagel M, Kruger S, et al: Combined molecular and clinical approach for decision making for surgery in HNPCC patients: A report on three cases in two families. Int J Colorectal Dis 16:402-407, 2001[CrossRef][Medline]
12. Kolodner RD, Tytell JD, Schmeits JL, et al: Germ-line msh6 mutations in colorectal cancer families. Cancer Res 59:5068-5074, 1999
13. Goodfellow PJ, Buttin BM, Herzog TJ, et al: Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers. Proc Natl Acad Sci U S A 100:5908-5913, 2003
14. Verma L, Kane MF, Brassett C, et al: Mononucleotide microsatellite instability and germline MSH6 mutation analysis in early onset colorectal cancer. J Med Genet 36:678-682, 1999
15. Wagner A, Hendriks Y, Meijers-Heijboer EJ, et al: Atypical HNPCC owing to MSH6 germline mutations: Analysis of a large Dutch pedigree. J Med Genet 38:318-322, 2001 16. Wijnen J, de Leeuw W, Vasen H, et al: Familial endometrial cancer in female carriers of MSH6 germline mutations. Nat Genet 23:142-144, 1999[CrossRef][Medline] 17. Plaschke J, Krüger S, Pistorius SR, et al: Involvement of hMSH6 in the development of hereditary and sporadic colorectal cancer revealed by immunostaining is based on germline mutations, but rarely on somatic inactivation. Int J Cancer 97:643-648, 2002[CrossRef][Medline]
18. Acharya S, Wilson T, Gradia S, et al: HMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6. Proc Natl Acad Sci U S A 93:13629-13634, 1996 19. Wu Y, Berends MJ, Mensink RG, et al: Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations. Am J Hum Genet 65:1291-1298, 1999[CrossRef][Medline] 20. Berends MJ, Wu Y, Sijmons RH, et al: Molecular and clinical characteristics of MSH6 variants: An analysis of 25 index carriers of a germline variant. Am J Hum Genet 70:26-37, 2002[CrossRef][Medline]
21. Vasen HF, Stormorken A, Menko FH, et al: MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: A study of hereditary nonpolyposis colorectal cancer families. J Clin Oncol 19:4074-4080, 2001 22. Vasen HF, Watson P, Mecklin JP, et al: New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC. Gastroenterology 116:1453-1456, 1999[CrossRef][Medline]
23. Rodriguez-Bigas MA, Boland CR, Hamilton SR, et al: A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting highlights and Bethesda guidelines. J Natl Cancer Inst 89:1758-1762, 1997
24. Boland CR, Thibodeau SN, Hamilton SR, 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 58:5248-5257, 1998
25. Dietmaier W, Wallinger S, Bocker T, et al: Diagnostic microsatellite instability: Definition and correlation with mismatch repair protein expression. Cancer Res 57:4749-4756, 1997 26. Plaschke J, Kruppa C, Tischler R, et al: Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer. Int J Cancer 85:606-613, 2000[CrossRef][Medline] 27. Holinski-Feder E, Muller-Koch Y, Friedl W, et al: DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2. J Biochem Biophys Methods 47:21-32, 2001[CrossRef][Medline] 28. Peterlongo P, Nafa K, Lerman GS, et al: MSH6 germline mutations are rare in colorectal cancer families. Int J Cancer 107:571-579, 2003[CrossRef][Medline] 29. Plaschke J, Kruger S, Dietmaier W, et al: Eight novel MSH6 germline mutations in patients with familial and nonfamilial colorectal cancer selected by loss of protein expression in tumor tissue. Hum Mutat 23:285, 2004 30. Shin KH, Ku JL, Park JG: Germline mutations in a polycytosine repeat of the hMSH6 gene in Korean hereditary nonpolyposis colorectal cancer. J Hum Genet 44:18-21, 1999[CrossRef][Medline] 31. Malkhosyan S, Rampino N, Yamamoto H, et al: M Frameshift mutator mutations. Nature 382:499-500, 1996[CrossRef][Medline]
32. Markowitz S, Wang J, Myeroff L, et al: Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability. Science 268:1336-1338, 1995
33. Baranovskaya S, Soto JL, Perucho M, et al: Functional significance of concomitant inactivation of hMLH1 and hMSH6 in tumor cells of the microsatellite mutator phenotype. Proc Natl Acad Sci U S A 98:15107-15112, 2001 34. Palombo F, Iaccarino I, Nakajima E, et al: HMutSbeta, a heterodimer of hMSH2 and hMSH3, binds to insertion/deletion loops in DNA. Curr Biol 6:1181-1184, 1996[CrossRef][Medline]
35. Plaschke J, Rüschoff J, Schackert HK: Genomic rearrangements of hMSH6 contribute to the genetic predisposition in suspected hereditary nonpolyposis colorectal cancer syndrome. J Med Genet 40:597-600, 2003 Submitted February 4, 2004; accepted June 24, 2004.
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Copyright © 2004 by the American Society of Clinical Oncology, Online ISSN: 1527-7755. Print ISSN: 0732-183X
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ABSTRACT
INTRODUCTION
protein complex (MSH2 + MSH6).
