Copyright
©The Author(s) 2005.
World J Gastroenterol. Oct 7, 2005; 11(37): 5770-5776
Published online Oct 7, 2005. doi: 10.3748/wjg.v11.i37.5770
Published online Oct 7, 2005. doi: 10.3748/wjg.v11.i37.5770
Table 1 Classification of colorectal cancer families, frequencies of pathogenic mutations in hMLH1 and hMSH2 genes and MSI phenotype
Clinical criteria | Number of families | hMLH1 mutations | MSH2 mutations | MSI-H | MSS | MSI untyped |
Amsterdam I | 56 | 17 | 15 | 42 | 13 | 1 |
Amsterdam II | 11 | 2 | 2 | 2 | 7 | 2 |
Bethesda | 37 | 5 | 0 | 6 | 20 | 11 |
HNPCC-like | 38 | 0 | 0 | 3 | 20 | 5 |
Total | 132 | 24 | 17 | 53 | 60 | 19 |
Table 2 hMSH6 mutations in Spanish HNPCC families
Family | Clinicalcriteria | Dx agedindex patient (y) | No. of tumorsin the family | Exon/intron | Nucleotidechange | Amino acidchange | Predictedconsequence | Nfdhtdata base |
3 | Bethesda | 42 | 1E, 1G, 1M, 1H, 1F, and 1A | Ex. 8 | c.3725 G > T | R1242L | Inconclusive | No |
11 | HNPCC-like | 58 | 1G, 2C, and 1B | Ex. 4 | c.2319 C > T | L773L | Inconclusive | No |
68 | Bethesda | 29 | 1L, and 1C | Ex. 4 | c.1164 C > T | H388H | Inconclusive | No |
Ex. 4 | c.2272 C>T | L758L | ||||||
81 | HNPCC-like | 50 | 4C | Int. 5 | c.3439?6 C > T | NA | Inconclusive | No |
94 | Amsterdam II | 45 | 3 P, 2E, 1G, and 3C | Ex. 4 | c.2633 T > C | V878A | Pathogenic | Yes |
100 | Amsterdam II | 54 | 4C, 1P, and 3G | Ex. 4 | c.706 C > T | Q236X | Truncation | No |
73 | Amsterdam | 29 | 2SM, 1G, 3C, and 1L | Ex. 4 | c.2633 T > C | V878A | Pathogenic | Yes |
121 | HNPCC-like | 58 | 3C, 1G, and 1B | Int. 5 | c.3439?6 C > T | NA | Inconclusive | No |
138 | Bethesda | 43 | 2C and 1 ureter in the same patient | Ex. 4 | c.1677 C > T | C559C | Inconclusive | No |
Table 3 hMSH6 polymorphisms in Spanish HNPCC families
Location | Nucleotidechange | Aminoacid change | Previouslyreported | Frequency1 |
Exon 1 | 116 G→A | G 39 E | Yes | 0.40 |
Exon 2 | 276 A→G | P 92 P | Yes | 0.38 |
Exon 3 | 540 T→C | D 180 D | Yes | 0.24 |
Exon 4 | 642 C→T | Y 214 Y | Yes | 0.25 |
Table 4 Molecular alterations of tumors from persons carrying mutations of hMSH6 gene
Family/member | Tumor type | MSI status | Immunohistochemistry | hMSH6 mutation | Other MMR gene mutation | ||
MLH1 | MSH2 | MSH6 | |||||
3/270 | CRC | MSI-H | P | P | P | R1242L | V716M (hMLH1) |
11/310 | CRC | MSI-H | P | P | P | L773L | NO |
68/675 | CRC | MSS | P | P | P | H388H and L758L | NO |
73/526 | 3 CRCs | MSI-H | P | P | N | V878A | NO |
81/757 | CRC | MSS | P | P | P | c.3439?6 C > T | K618A (hMLH1) |
94/854 | UTERO | MSI-H | P | P | N | V878A | K618A (hMLH1) |
100/940 | CRC | MSS | P | P | N | Q236X | NO |
121/1041 | CRC | MSS | ND | ND | ND | c.3439?6 C > T | NO |
138/1165 | 2 CRCs | MSI-H | P | P | P | C559C | P350P (hMLH1) |
- Citation: Abajo AS, Hoya ML, Tosar A, Godino J, Fernández JM, Asenjo JL, Villamil BP, Segura PP, Diaz-Rubio E, Caldes T. Low prevalence of germline hMSH6 mutations in colorectal cancer families from Spain. World J Gastroenterol 2005; 11(37): 5770-5776
- URL: https://www.wjgnet.com/1007-9327/full/v11/i37/5770.htm
- DOI: https://dx.doi.org/10.3748/wjg.v11.i37.5770