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DOI: 10.1055/s-0043-1777449
Screening for Mutations in Hereditary Cancer Susceptibility Genes in a Region with High Endogamy in Brazil
Abstract
Introduction Cancer is a multifactorial disease dependent on the influence of genetic and environmental factors. About 10% of cancers are associated with germline mutations, which predispose to a higher risk of developing cancer. Currently, the use of panels that identify susceptibility and/or association genes cancer has been increasingly used, both in clinical practice and in scientific research.
Objective To investigate genetic mutations in patients with a profile for hereditary cancer in individuals from a region of northeast Brazil, where there is a high frequency of endogenous and consanguineous marriages.
Methods A set of 17 genes (BRCA1, BRCA2, APC, TP53, PTEN, RET, VHL, RB1, CDKN2, CDH1, CHEK2, MLH1, MSH2, MSH6, MUTYH, XPA, and XPC) associated with cancer and hereditary syndromes were analyzed. Fifteen patients with a hereditary cancer profile were evaluated.
Results The pathogenic variant found was c.1187G > A (p.Gly396Asp), rs36053993 in the MUTYH gene in a male patient diagnosed with melanoma at the age of 43 years and a family history for this tumor. This gene encodes an important enzyme related to DNA repair and has been associated with other types of cancer, this is the first report of an association with melanoma, the biological plausibility of this association is given once the MUTYH protein is expressed in the skin tissue and is responsible for repairing damage caused, for example, by sun exposure.
Conclusion The results of this study suggest that this mutation may be important for the hereditary predisposition to melanoma, but a broader investigation of this mutation is needed.
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Introduction
All cancers are caused by genetic material changes, but only a small proportion (5–10%) is due to inherited mutations.[1] Therefore, the identification of individuals carrying pathogenic variants in hereditary cancer susceptibility genes allows: early screening and risk reduction protocol implementation.[2]
Molecular diagnostic tests for hereditary cancer have traditionally been restricted to the analysis of one or a few genes, selected from the syndrome identified in the family.[3] However, cancer susceptibility may occur due to one or more mutations in one of several different genes related to tumor development, not necessarily related to clinical suspect.[4] Due to genetic heterogeneity, the mutation responsible for the disease is not always in a gene classically related to that syndrome, as in the case of the BRCA1 and BRCA2 genes in King's syndrome.[3] [5] Thus, polygenetic assessment using next-generation sequencing (NGS) has been the most suitable method for investigating genetic variants associated with cancer risk, in addition to presenting cost and analysis time efficiency.[6]
The criteria used to select patients at risk for hereditary cancer are often based on self-reported family history.[6] However, the absence of supporting documents (medical records, death certificate) and inaccurate information reported by patients can reduce the reliability of the information and thus restrict the use of this tool in clinical practice and in decision-making on primary surveillance recommendations and preventive measures interventions.[7] However, in Brazil, researches suggested that for middle- and low-income individuals, the use of this information, even without supporting documents, has been useful for screening patients with hereditary cancer.[8]
In this study, we selected a sample of cancer patients from Monte Santo, a municipality located in the northeast region of Brazil. This city is characterized by a low level of education, a situation of extreme poverty, a low rate of immigration, a high rate of inbreeding, and consanguinity.[9] In addition, in Monte Santo, it was observed that some rare genetic diseases have a high frequency, for example, mucopolysaccharidosis type VI (1:5,000 in Monte Santo, reaching 1:1,500,000 worldwide).[10] Due to the characteristics of this population, we started a community genetics project that includes a census of diseases with probable genetic etiologies in the population, including cancer. Thus, the objective of this work was to investigate the mutational profile of patients with suspected hereditary cancer using a multigene panel through NGS.
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Materials and Methods
Sample
During the period from August 2014 to June 2016, 116 patients diagnosed with any type of cancer in Monte Santo, Bahia (northeast Brazil) were included in the study. Of these, 30 patients with hereditary cancer characteristics were selected using the criteria: family history for the disease and age of cancer occurrence before 50 years,[11] in addition, the patients should not be related. For all participants, a questionnaire was filled out with personal and clinical data and race information by self-report according to the criteria of the Brazilian Institute of Geography and Statistics. This study was approved by the Ethics Committee of the Hospital University Prof Edgar Santos, and all subjects provided informed consent.
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Multigene Panel
The panel was composed of 17 genes, which: BRCA1, BRCA2, APC, TP53, PTEN, RET, VHL, RB1, CDKN2, CDH1, CHECK2, MLH1, MSH2, MSH6, MUTYH, XPA, and XPC. These genes were selected because they are associated with different cancer types and hereditary syndromes. DNA sample was obtained from 200 µL of peripheral blood using the Mini Spin Plus Extraction Kit (Biometrix, BioPur, Curitiba, Paraná, Brazil) according to the manufacturer's instructions. All DNA samples were quantified by spectrophotometry in a NanoDrop 2000c Spectrophotometer device (ThermoScientific, Wilmington, Delaware, United States) at 260/280 nm wavelengths. DNA integrity was verified in a 2.5% agarose gel and subsequently diluted to a concentration of 25 ng/µL. The panel used was TruSeq Custom Amplicon v1.5 on the MiSeq System (Illumina, San Diego, California, United States). The variants were classified according to the ClinVar database into: pathogenic, variant of uncertain significance (VUS), and of pharmacogenetic importance ([Supplementary Table S1]).
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Results
Fifteen patients (4 women and 11 men), of the 30 who were selected, were possible to carry out the multigene panel. Most women had breast cancer (3/5) and among men, prostate cancer (2/11), and skin cancer (2/11) were the most frequent ([Table 1]). The mean age at diagnosis was 47.8 years ± 12.87, and among those with a family history, it was 51.2 and without a family history, 41 years.
Patient |
Tumor site |
Gender |
Age at diagnosis (y) |
SR |
Family history[a] |
---|---|---|---|---|---|
1 |
Stomach |
M |
47 |
White |
No |
2 |
Skin (squamocellular) |
M |
41 |
Brown |
No |
3 |
Breast |
F |
39 |
Brown |
No |
4 |
Rectum |
F |
66 |
White |
Yes |
5 |
Prostate |
M |
52 |
Brown |
Yes |
6 |
Breast |
F |
44 |
White |
Yes |
7 |
Prostate |
M |
60 |
Brown |
Yes |
8 |
Skin (melanoma) |
M |
43 |
White |
Yes |
9 |
Breast |
F |
50 |
Brown |
No |
10 |
Breast |
F |
50 |
Brown |
Yes |
11 |
Breast |
F |
28 |
Brown |
No |
12 |
Intestine |
M |
69 |
Brown |
Yes |
13 |
Brain |
M |
25 |
Brown |
Yes |
14 |
Thyroid |
F |
40 |
Brown |
Yes |
15 |
Prostate |
M |
63 |
Black |
Yes |
Abbreviation: SR, self-report.
Seven clinically important variants were found in 12 patients (58%) ([Table 2]). Of these, 11 patients (73.3%) had some variant of pharmacogenetic importance and 1 patient (6.6%) has a pathogenic variant. All variants found were in heterozygosity. Four VUS were identified in four (26.6%) patients in the genes: APC, BRCA2, and MUTYH. One of the patients had two different VUS ([Supplementary Table S2]).
Abbreviation: VUS, variant of uncertain significance.
Notes: Pharmacogenetics A: cisplatin toxicity. Pharmacogenetics B: cisplatin, cyclophosphamide, Fluoratil, and paclitaxel toxicity.
Each VUS was found in only one patient. For variants with pharmacogenetic importance, most patients (9/15) had the XPC:c.2815C > A variant (p.Gln939Lys) and the others (5/15) had the TP53:c.215C > G variant (p.Pro72Arg). The pathogenic variant MUTYH:c.1187G > A (p.Gly396Asp) was found in a male patient diagnosed with melanoma at the age of 43 years and with a family history of this tumor. The pedigree of the family history is shown in [Fig. 1].
![](https://www.thieme-connect.de/media/10.1055-s-00046370/202304/thumbnails/10-1055-s-0043-1777449-i2300074-1.jpg)
![Zoom Image](/products/assets/desktop/css/img/icon-figure-zoom.png)
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Discussion
In the analyzed sample, 1/16 (6.25%) patients with pathogenic mutation and 4/16 (25%) patients with VUS were identified. In a study carried out using a multigene panel with 12 genes for different cancer types and using the same criteria for cases selection in the present study (age <50 years and/or family history), 12.3% of patients had a pathogenic mutation and 19.4% patients with VUS.[12]
Two pharmacologically important polymorphisms were found: p.(Gln939Lys) in the XPC gene (in 9/15 participants) and p.(Pro72Arg) in the TP53 gene (5/15 participants). According to the 1000 Genomes Project, the XPC mutation p.(Gln939Lys) has a high frequency of the T allele in parental populations: African (0.7315) and European (0.5421) (no data in Amerindian population). The TP53 p.(Pro72Arg) mutation, on the other hand, has a variable frequency of the G allele between African (0.6389) and European (0.2757) populations (no data in Amerindian population). The results observed are in agreement with what is expected for a mixed population as Brazil, especially the northeast Brazilian, which has a high African and European ancestral contribution.[13] [14] Due to the lack of data on the treatment performed by the patients, it was not possible to use the information on the pharmacogenetically important markers found and the effect on the therapeutic approach used.
For the MUTYH gene, more than 300 mutations have been described according to the Leiden Open Variation Database variant database.[15] Among them, the missense mutation found in this study p.(Gly396Asp) described as pathogenic by ClinVar (https://preview.ncbi.nlm.nih.gov/clinvar/variation/5294/). This amino acid is located in the C-terminal domain of the protein (exon 13) and its replacement reduces the interaction between enzyme and substrate, compromising enzymatic activity.[16] [17] This is one of the main variants that predispose to MUTYH-associated polyposis (MAP),[18] a hereditary syndrome whose main clinical manifestations are the early development of multiple adenomatous polyps along the intestine and colorectal cancer (CRC). However, in addition to these, other extraintestinal manifestations can occur in patients with MAP, including skin findings (benign and malignant).[19] [20] In a cohort of patients with MAP followed up, the occurrence of extraintestinal tumors and skin cancer was the second most common cancer reported, with a significant incidence (standardized incidence ratio: 2.8; 95% confidence interval: 1.5–4.8). In that study, of the 13 patients with skin cancer, 5 had the p.Gly396Asp mutation and of these, 2 were diagnosed with melanoma.[20] In contradiction, another study found no association between the risk of melanoma development or aggressiveness and this variant.[21]
The MUTYH:p.(Gly396Asp) mutation has a higher frequency in populations of Caucasian origin (0.0089 Europeans, 0.0043 Amerindians, 0.0000 Africans) according to the 1000 Genome, and its origin has been estimated at about 6,000 to 9,000 years B.C.[22] This finding is in agreement with the present study that found the mutation in a patient with phenotypic characteristics of Europeans and with self-reported as white. In Brazil, this variant has already been described in two different studies: 3/60 patients with clinical criteria for MAP, one of the cases being homozygous[23] and 1/23 mutation-positive patients with < 100 polyps.[24] Thus, finding the mutation in 1/16 patients without criteria for MAP, but with a family history of melanoma reinforces the association of mutations in the MUTYH gene with other types of tumors.[25]
It is important to consider the presence of MUTYH:p.(Gly396Asp) mutation in a patient with melanoma to justify the tumor origin, these data can be supported by the studies presented below. In principle, it is plausible to consider that epithelial tissue is exposed to the action of reactive oxygen species after ultraviolet (UV) exposure and that the presence of an efficient repair mechanism in this tissue is necessary. In fact, it has already been shown that the origin of melanoma may be related to oxidative damage specifically due to the presence of 8-oxoG molecules.[26] [27] Thus, the defect in enzymes that act in the base excision repair mechanism may be important in the understanding of this tumor; however, MUTYH does not act in isolation. For example, skin cancer susceptibility has been demonstrated in OGG1-knockout mice with 8-oxoG production in the genetic material of UVB-exposed epidermal cells.[28] The OGG1 gene encodes the 8-oxoG DNA glycosylase enzyme (OGG1) that recognizes and removes 8-oxoG, preventing future base mismatches. The involvement of the MUTYH gene in the development of melanoma was suggested in the study by Ogbah et al (2012)[29] after evaluating different cell lines of this type of cancer through multiplex ligation-dependent probe amplification probes that identified loss of gene heterozygosity. Furthermore, a relationship between altered MUTYH and OGG1 function was observed with various tumors: neuroendocrine intestinal cells in humans, as well as risk of lung, hepatocellular and cervical cancer.[30] [31] In fact, according to the Human Protein Atlas, the MUTYH protein is expressed in epithelial tissue as well as in melanoma, although in smaller amounts when compared with other tissues of the digestive system (stomach, duodenum, colon, and rectum).[32] On the contrary, OGG1 is highly expressed, both in epithelial cells and in melanoma cells, probably due to its preventive effect and prior to the action of MUTYH. Mutations in MUTYH may contribute to carcinogenesis, as the protein acts to prevent mutagenesis, it activates a programmed cell death pathway triggered by the 8-oxoG accumulation in nuclear and mitochondrial DNA through the activation of the Ca2+-dependent protease, calpain.[33] It was later shown that this pathway could still be PARP/MLH1 dependent mediating the activity of p53, tumor suppressor protein.[34] It is already known that downregulation of calpain-3 and MLH1 inactivation are events that contribute to the progression of melanoma, reinforcing the importance of MUTYH functionality.[35] [36] [37] So, in the absence of MUTYH, such premutagenic or precancerous cells could survive and have a higher mutation rate in proto-oncogenes or tumor suppressor genes due to increased levels of 8-oxoG.
It is interesting to consider that the pathogenic mutations in MUTYH associated with hereditary cancer have been mostly reported in homozygosity, with the complete inactivation of its product. However, it has been suggested that the risk of developing CRC is higher in both heterozygous and homozygous MUTYH mutant individuals than in individuals without pathogenic alleles, even those with a family history of CRC.[38] In a study with neuroendocrine tumors of the small intestine, in which the presence of the p.Gly396Asp mutation was detected in heterozygosity in 6/24 patients with and without a family history, it was suggested that the biallelic inactivation of MUTYH may not be the only mechanism that drove tumor development and that additional mutations in OGG1 would be important for the pathogenesis of the disease.[31] In view of the presented data and the available literature, it is possible to suggest that the presence of a mutation in the MUTYH gene in heterozygosis may be responsible for a less aggressive phenotype, with late onset and slow tumor progression. In the literature, an association has already been observed between high risk for breast cancer and the variant found in the present study in heterozygosis.[39]
It is important to emphasize that the patient with a pathogenic mutation in the present study has a family history of melanoma and that no alterations were found in CDKN2, the gene responsible for susceptibility in approximately 22% of familial cases with a single mutation and in more than half of the individuals diagnosed with multiple primary melanomas.[40] With this, it is still possible to suggest that other genes of lesser relevance are involved in the disease process, such as the OGG1 gene.
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Conclusion
The results of this study suggest that through the selection of patients with a hereditary cancer profile, it was possible to identify mutations of clinical importance, such as those of pharmacogenetic importance, of uncertain significance (VUS) and pathogenic mutations, even in a small sample of individuals. The use of a multigenic panel made it possible to identify the pathogenic mutation MUTYH p.(Gly396Asp) in a patient with melanoma and a family history. Mutations in this gene have been poorly studied in patients with this neoplasm, but the biological plausibility indicates that there is evidence for this association and thus justifies the expansion of the study. This is also an advantage of multiple gene analysis, where new associations can be identified.
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Conflict of Interest
None declared.
Authors' Contribution
All authors made substantial contributions to the intellectual content of this article.
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- 2 Foretová L. Hereditary cancer syndromes, their testing and prevention. Cas Lek Cesk 2019; 158 (01) 15-21
- 3 Katsanis SH, Katsanis N. Molecular genetic testing and the future of clinical genomics. Nat Rev Genet 2013; 14 (06) 415-426
- 4 Webster P, Dawes JC, Dewchand H. et al. Subclonal mutation selection in mouse lymphomagenesis identifies known cancer loci and suggests novel candidates. Nat Commun 2018; 9 (01) 2649 . [published correction appears in Nat Commun 2019 Mar 6;10(1):1167]
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- 11 Selkirk CG, Vogel KJ, Newlin AC. et al. Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice. Fam Cancer 2014; 13 (04) 527-536
- 12 Hermel DJ, McKinnon WC, Wood ME, Greenblatt MS. Multi-gene panel testing for hereditary cancer susceptibility in a rural Familial Cancer Program. Fam Cancer 2017; 16 (01) 159-166
- 13 Santos HC, Horimoto AV, Tarazona-Santos E. et al; Brazilian EPIGEN Project Consortium. A minimum set of ancestry informative markers for determining admixture proportions in a mixed American population: the Brazilian set. Eur J Hum Genet 2016; 24 (05) 725-731
- 14 Pereira V, Santangelo R, Børsting C. et al. Evaluation of the precision of ancestry inferences in South American admixed populations. Front Genet 2020; 11: 966
- 15 Out AA, Tops CM, Nielsen M. et al. Leiden Open Variation Database of the MUTYH gene. Hum Mutat 2010; 31 (11) 1205-1215
- 16 Banda DM, Nuñez NN, Burnside MA, Bradshaw KM, David SS. Repair of 8-oxoG:A mismatches by the MUTYH glycosylase: mechanism, metals and medicine. Free Radic Biol Med 2017; 107: 202-215
- 17 D'Agostino VG, Minoprio A, Torreri P. et al. Functional analysis of MUTYH mutated proteins associated with familial adenomatous polyposis. DNA Repair (Amst) 2010; 9 (06) 700-707
- 18 Magrin L, Fanale D, Brando C. et al. MUTYH-associated tumor syndrome: the other face of MAP. Oncogene 2022; 41 (18) 2531-2539
- 19 Haimov D, Lieberman S, Castellvi-Bel S, Nielsen M, Goldberg Y. Nonmalignant features associated with inherited colorectal cancer syndromes-clues for diagnosis. Cancers (Basel) 2022; 14 (03) 628
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- 21 Santonocito C, Paradisi A, Capizzi R. et al. Common genetic variants of MUTYH are not associated with cutaneous malignant melanoma: application of molecular screening by means of high-resolution melting technique in a pilot case-control study. Int J Biol Markers 2011; 26 (01) 37-42
- 22 Aretz S, Tricarico R, Papi L. et al. MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events. Eur J Hum Genet 2014; 22 (07) 923-929
- 23 Pitroski CE, Cossio SL, Koehler-Santos P, Graudenz M, Prolla JC, Ashton-Prolla P. Frequency of the common germline MUTYH mutations p.G396D and p.Y179C in patients diagnosed with colorectal cancer in Southern Brazil. Int J Colorectal Dis 2011; 26 (07) 841-846
- 24 Torrezan GT, da Silva FC, Santos EM. et al. Mutational spectrum of the APC and MUTYH genes and genotype-phenotype correlations in Brazilian FAP, AFAP, and MAP patients. Orphanet J Rare Dis 2013; 8: 54
- 25 Nielsen M, Infante E, Brand R. MUTYH polyposis. In: Adam MP, Mirzaa GM, Pagon RA. et al, eds. GeneReviews®. Seattle (WA): University of Washington,; Seattle; 2012
- 26 Hintsala HR, Jokinen E, Haapasaari KM. et al. Nrf2/Keap1 pathway and expression of oxidative stress lesions 8-hydroxy-2′-deoxyguanosine and nitrotyrosine in melanoma. Anticancer Res 2016; 36 (04) 1497-1506
- 27 Nishisgori C. Current concept of photocarcinogenesis. Photochem Photobiol Sci 2015; 14 (09) 1713-1721
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- 31 Dumanski JP, Rasi C, Björklund P. et al. A MUTYH germline mutation is associated with small intestinal neuroendocrine tumors. Endocr Relat Cancer 2017; 24 (08) 427-443
- 32 Uhlén M, Fagerberg L, Hallström BM. et al. Proteomics. Tissue-based map of the human proteome. Science 2015; 347 (6220) 1260419
- 33 Oka S, Nakabeppu Y. DNA glycosylase encoded by MUTYH functions as a molecular switch for programmed cell death under oxidative stress to suppress tumorigenesis. Cancer Sci 2011; 102 (04) 677-682
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- 35 Ponti G, Losi L, Pellacani G. et al. Malignant melanoma in patients with hereditary nonpolyposis colorectal cancer. Br J Dermatol 2008; 159 (01) 162-168
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Address for correspondence
Publication History
Article published online:
08 December 2023
© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)
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References
- 1 Baranova EE, Bodunova NA, Vorontsova МV. et al. [Hereditary cancer syndromes: a modern paradigm]. Probl Endokrinol (Mosk) 2020; 66 (04) 24-34
- 2 Foretová L. Hereditary cancer syndromes, their testing and prevention. Cas Lek Cesk 2019; 158 (01) 15-21
- 3 Katsanis SH, Katsanis N. Molecular genetic testing and the future of clinical genomics. Nat Rev Genet 2013; 14 (06) 415-426
- 4 Webster P, Dawes JC, Dewchand H. et al. Subclonal mutation selection in mouse lymphomagenesis identifies known cancer loci and suggests novel candidates. Nat Commun 2018; 9 (01) 2649 . [published correction appears in Nat Commun 2019 Mar 6;10(1):1167]
- 5 Gardner SA, Weymouth KS, Kelly WS. et al. Evaluation of a 27-gene inherited cancer panel across 630 consecutive patients referred for testing in a clinical diagnostic laboratory. Hered Cancer Clin Pract 2018; 16: 1
- 6 Price KS, Svenson A, King E, Ready K, Lazarin GA. Inherited cancer in the age of next-generation sequencing. Biol Res Nurs 2018; 20 (02) 192-204
- 7 Miroševič Š, Klemenc-Ketiš Z, Peterlin B. Family history tools for primary care: A systematic review. Eur J Gen Pract 2022; 28 (01) 75-86
- 8 Flória-Santos M, Lopes-Júnior LC, Alvarenga LdeM. et al. Self-reported cancer family history is a useful tool for identification of individuals at risk of hereditary cancer predisposition syndrome at primary care centers in middle-income settings: a longitudinal study. Genet Mol Biol 2016; 39 (02) 178-183
- 9 Machado TM, Bomfim TF, Souza LV. et al. Types of marriages, population structure and genetic disease. J Biosoc Sci 2013; 45 (04) 461-470 . [published correction appears in J Biosoc Sci 2013 Jul;45(4):575]
- 10 Costa-Motta FM, Bender F, Acosta A. et al. A community-based study of mucopolysaccharidosis type VI in Brazil: the influence of founder effect, endogamy and consanguinity. Hum Hered 2014; 77 (1-4): 189-196
- 11 Selkirk CG, Vogel KJ, Newlin AC. et al. Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice. Fam Cancer 2014; 13 (04) 527-536
- 12 Hermel DJ, McKinnon WC, Wood ME, Greenblatt MS. Multi-gene panel testing for hereditary cancer susceptibility in a rural Familial Cancer Program. Fam Cancer 2017; 16 (01) 159-166
- 13 Santos HC, Horimoto AV, Tarazona-Santos E. et al; Brazilian EPIGEN Project Consortium. A minimum set of ancestry informative markers for determining admixture proportions in a mixed American population: the Brazilian set. Eur J Hum Genet 2016; 24 (05) 725-731
- 14 Pereira V, Santangelo R, Børsting C. et al. Evaluation of the precision of ancestry inferences in South American admixed populations. Front Genet 2020; 11: 966
- 15 Out AA, Tops CM, Nielsen M. et al. Leiden Open Variation Database of the MUTYH gene. Hum Mutat 2010; 31 (11) 1205-1215
- 16 Banda DM, Nuñez NN, Burnside MA, Bradshaw KM, David SS. Repair of 8-oxoG:A mismatches by the MUTYH glycosylase: mechanism, metals and medicine. Free Radic Biol Med 2017; 107: 202-215
- 17 D'Agostino VG, Minoprio A, Torreri P. et al. Functional analysis of MUTYH mutated proteins associated with familial adenomatous polyposis. DNA Repair (Amst) 2010; 9 (06) 700-707
- 18 Magrin L, Fanale D, Brando C. et al. MUTYH-associated tumor syndrome: the other face of MAP. Oncogene 2022; 41 (18) 2531-2539
- 19 Haimov D, Lieberman S, Castellvi-Bel S, Nielsen M, Goldberg Y. Nonmalignant features associated with inherited colorectal cancer syndromes-clues for diagnosis. Cancers (Basel) 2022; 14 (03) 628
- 20 Vogt S, Jones N, Christian D. et al. Expanded extracolonic tumor spectrum in MUTYH-associated polyposis. Gastroenterology 2009; 137 (06) 1976-85.e1 , 10
- 21 Santonocito C, Paradisi A, Capizzi R. et al. Common genetic variants of MUTYH are not associated with cutaneous malignant melanoma: application of molecular screening by means of high-resolution melting technique in a pilot case-control study. Int J Biol Markers 2011; 26 (01) 37-42
- 22 Aretz S, Tricarico R, Papi L. et al. MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events. Eur J Hum Genet 2014; 22 (07) 923-929
- 23 Pitroski CE, Cossio SL, Koehler-Santos P, Graudenz M, Prolla JC, Ashton-Prolla P. Frequency of the common germline MUTYH mutations p.G396D and p.Y179C in patients diagnosed with colorectal cancer in Southern Brazil. Int J Colorectal Dis 2011; 26 (07) 841-846
- 24 Torrezan GT, da Silva FC, Santos EM. et al. Mutational spectrum of the APC and MUTYH genes and genotype-phenotype correlations in Brazilian FAP, AFAP, and MAP patients. Orphanet J Rare Dis 2013; 8: 54
- 25 Nielsen M, Infante E, Brand R. MUTYH polyposis. In: Adam MP, Mirzaa GM, Pagon RA. et al, eds. GeneReviews®. Seattle (WA): University of Washington,; Seattle; 2012
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- 27 Nishisgori C. Current concept of photocarcinogenesis. Photochem Photobiol Sci 2015; 14 (09) 1713-1721
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