BMC Medical Genetics最新文献

{"title":"Two novel PCDH19 mutations in Russian patients with epilepsy with intellectual disability limited to females: a case report.","authors":"Anastasiya Aleksandrovna Kozina,&nbsp;Elena Grigorievna Okuneva,&nbsp;Natalia Vladimirovna Baryshnikova,&nbsp;Inessa Dmitrievna Fedonyuk,&nbsp;Alexey Aleksandrovich Kholin,&nbsp;Elena Stepanovna Il'ina,&nbsp;Anna Yurievna Krasnenko,&nbsp;Ivan Fedorovich Stetsenko,&nbsp;Nikolay Alekseevich Plotnikov,&nbsp;Olesia Igorevna Klimchuk,&nbsp;Ekaterina Ivanovna Surkova,&nbsp;Valery Vladimirovich Ilinsky","doi":"10.1186/s12881-020-01119-6","DOIUrl":"https://doi.org/10.1186/s12881-020-01119-6","url":null,"abstract":"<p><strong>Background: </strong>Epilepsy with intellectual disability limited to females (Epileptic encephalopathy, early infantile, 9; EIEE9) is a rare early infantile epileptic encephalopathy characterized by an unusual X-linked inheritance: females with heterozygous mutations are affected, while hemizygous males are not.</p><p><strong>Case presentation: </strong>We describe the clinical and molecular characteristics of 2 Russian patients with EIEE9 (females, ages 3 years and 7 years). In these patients seizures developed at the age of 3 years. Additionally, for our patients and for cases described in the literature we searched for a possible relationship between the type and localization of the mutation and the EIEE9 clinical phenotype.</p><p><strong>Conclusions: </strong>We identified two novel PCDH19 mutations in EIEE9 patients: a missense mutation in exon 1 (c.1236C > A, p.Asp412Glu) and a frameshift in exon 3 (c.2386_2387insGTCT, p.Thr796fs). We conclude that the age of seizure onset and the presence of intellectual disability may depend not on the type and localization of PCDH19 mutations, but on the X-inactivation status. The study also highlights the need to screen for EIEE9 among young female epilepsy patients.</p>","PeriodicalId":9015,"journal":{"name":"BMC Medical Genetics","volume":" ","pages":"209"},"PeriodicalIF":0.0,"publicationDate":"2020-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12881-020-01119-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38610627","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Development of an immunogenomic landscape for the competing endogenous RNAs network of peri-implantitis.","authors":"Yang Li,&nbsp;Jina Zheng,&nbsp;Chanjuan Gong,&nbsp;Kengfu Lan,&nbsp;Yuqing Shen,&nbsp;Xiaojun Ding","doi":"10.1186/s12881-020-01145-4","DOIUrl":"https://doi.org/10.1186/s12881-020-01145-4","url":null,"abstract":"<p><strong>Background: </strong>Peri-implantitis is an inflammation that occurs around the implant, resulting in varying degrees of inflammatory damage to the soft and hard tissues. The characteristic criterion is the loss of the supporting bone in an inflammatory environment. However, the specific mechanisms and biomarkers involved in peri-implantitis remain to be further studied. Recently, competing endogenous RNAs (ceRNA) and immune microenvironment have been found to play a more important role in the inflammatory process. In our study, we analyzed the expression of immune related microRNAs (miRNAs), long noncoding RNAs (lncRNAs) and message RNAs (mRNAs) in peri-implantitis by analyzing GSE33774 and GSE57631.</p><p><strong>Methods: </strong>In this study, we explored the expression profile data of immune-related lncRNAs, miRNAs and mRNAs, and constructed immune-related ceRNA network involved in the pathogenesis of peri-implantitis. In addition, the CIBERSORT was used to evaluate the content of immune cells in normal tissues and peri-implantitis to detect the immune microenvironment of peri-implantitis.</p><p><strong>Results: </strong>In the analysis, 14 DElncRNAs, 16 DEmiRNAs, and 18 DEmRNAs were used to establish an immune related ceRNA network and the immune infiltration patterns associated with peri-implantitis was discovered. Through the mutual verification of the two datasets, we found that GSK3B and miR-1297 may have important significance in the immune microenvironment and pathogenesis of peri-implantitis and GSK3B was closely related to four types of immune cells, especially with the highest correlation with resting mast cells (P = 0.0003).</p><p><strong>Conclusions: </strong>Through immune-related ceRNA network, immune-related genes (IRGs) and immune cell infiltration can further comprehensively understand the pathogenesis of peri-implantitis, which built up an immunogenomic landscape with clinical significance for peri-implantitis.</p>","PeriodicalId":9015,"journal":{"name":"BMC Medical Genetics","volume":" ","pages":"208"},"PeriodicalIF":0.0,"publicationDate":"2020-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12881-020-01145-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38510689","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Investigation of INDEL variants in apoptosis: the relevance to gastric cancer.","authors":"Giovanna Chaves Cavalcante, Milene Raiol de Moraes, Cristina Maria Duarte Valente, Caio Santos Silva, Antônio André Conde Modesto, Paula Baraúna de Assumpção, Paulo Pimentel de Assumpção, Sidney Santos, Ândrea Ribeiro-Dos-Santos","doi":"10.1186/s12881-020-01138-3","DOIUrl":"10.1186/s12881-020-01138-3","url":null,"abstract":"<p><strong>Background: </strong>Apoptosis is a type of cell death involved in different pathways inherent to the cell and the evasion from this mechanism has been related to cancer, although this process remains not very well comprehended. Gastric cancer (GC) is one of the most incident and aggressive types of cancer worldwide. In this study, we analyzed the distribution of INDEL variants in GC patients (Case) and individuals from the general population (Control) from the Amazon region, in which GC is remarkably frequent.</p><p><strong>Methods: </strong>A panel of nine INDEL markers in apoptosis-related genes (BCL2 rs11269260, CASP3 rs4647655, CASP8 rs3834129 and rs59308963, CASP9 rs4645982 and rs61079693, FADD rs4197, FAS rs10562972 and TP53 rs17880560) was developed and genotyped by multiplex PCR in both groups.</p><p><strong>Results: </strong>In our analyses, only marker rs4197 (FADD gene) was associated to GC development as follows: INS/DEL genotype of rs4197 increasing in about 2-fold the chances of developing this type of cancer (P = 0.046; OR = 1.940; 95%CI = 1.011-3.725).</p><p><strong>Conclusion: </strong>Our results suggest that rs4197 (FADD gene) might play a role in gastric carcinogenesis in the investigated population. More studies are needed to clarify this relation. Here, we highlight the importance of investigating INDEL variants in genes involved in apoptosis.</p>","PeriodicalId":9015,"journal":{"name":"BMC Medical Genetics","volume":" ","pages":"207"},"PeriodicalIF":0.0,"publicationDate":"2020-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7574166/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38505468","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"p.Arg72Pro polymorphism of P53 and breast cancer risk: a meta-analysis of case-control studies.","authors":"Brehima Diakite,&nbsp;Yaya Kassogue,&nbsp;Guimogo Dolo,&nbsp;Jun Wang,&nbsp;Erin Neuschler,&nbsp;Oumar Kassogue,&nbsp;Mamadou L Keita,&nbsp;Cheick B Traore,&nbsp;Bakarou Kamate,&nbsp;Etienne Dembele,&nbsp;Sellama Nadifi,&nbsp;Robert L Murphy,&nbsp;Seydou Doumbia,&nbsp;Lifang Hou,&nbsp;Mamoudou Maiga","doi":"10.1186/s12881-020-01133-8","DOIUrl":"https://doi.org/10.1186/s12881-020-01133-8","url":null,"abstract":"<p><strong>Background: </strong>The effect of the p.Arg72Pro variant of the P53 gene on the risk of development ofbreast cancer remains variable in populations. However, the use ofstrategies such aspoolingage-matched controls with disease may provide a consistent meta-analysis. Our goal was to perform a meta-analysis in order to assess the association of p.Arg72Pro variant of P53 gene with the risk of breast cancer.</p><p><strong>Methods: </strong>Databases such as PubMed, Genetics Medical Literature, Harvard University Library, Web of Science and Genesis Library were used to search articles. Case-control studies with age-matched on breast cancer havingevaluated the genotype frequencies of the TP53 p.Arg72Pro polymorphism were selected. The fixed and random effects (Mantel-Haenszel) were calculated using pooled odds ratio of 95% CI to determine the risk of disease. Inconsistency was calculated to determine heterogeneity among the studies. The publication bias was estimated using the funnel plot.</p><p><strong>Results: </strong>Twenty-one publications with 7841 cases and 8876 controls were evaluated in this meta-analysis. Overall, our results suggested that TP53 p.Arg72Pro was associated with the risk of breast cancer for the dominant model (OR = 1.09, 95% CI = 1.02-1.16, P = 0.01) and the additive model (OR = 1.09, 95% CI = 1.01-1.17, P = 0.03), but not for the recessive model (OR = 1.07, 95% CI = 0.97-1.18, P = 0.19). According to the ethnic group analysis, Pro allele was associated with the risk of breast cancer in Caucasians for the dominant model and additive model (P = 0.02), and Africans for the recessive model and additive model (P = 0.03).</p><p><strong>Conclusions: </strong>This meta-analysis found a significant association between TP53 p.Arg72Pro polymorphism and the risk of breast cancer. Individuals carrying at least one Pro allele were more likely to have breast cancer than individuals harboring the Arg allele.</p>","PeriodicalId":9015,"journal":{"name":"BMC Medical Genetics","volume":" ","pages":"206"},"PeriodicalIF":0.0,"publicationDate":"2020-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12881-020-01133-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38602066","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Effect of DNMT3A polymorphisms on CpG island hypermethylation in gastric mucosa.","authors":"Hikaru Takano,&nbsp;Tomoyuki Shibata,&nbsp;Masakatsu Nakamura,&nbsp;Naoko Sakurai,&nbsp;Tasuku Hayashi,&nbsp;Masafumi Ota,&nbsp;Tomoe Nomura-Horita,&nbsp;Ranji Hayashi,&nbsp;Takeo Shimasaki,&nbsp;Toshimi Otsuka,&nbsp;Tomomitsu Tahara,&nbsp;Tomiyasu Arisawa","doi":"10.1186/s12881-020-01142-7","DOIUrl":"https://doi.org/10.1186/s12881-020-01142-7","url":null,"abstract":"<p><strong>Background: </strong>CpG methylation of tumor suppressor genes occurs in the early stage of carcinogenesis. Detecting risk factors for aberrant CpG methylation is clinically important for predicting cancer development. DNA methyltransferase (DNMT) 3a is considered to play critical roles in the DNA methylation process during pathogenesis. In this study, we evaluated the association between DNMT3A polymorphisms (rs6733868 and rs13428812) and CpG methylation status in non-cancerous gastric mucosa.</p><p><strong>Methods: </strong>We determined the DNMT3A genotype and CpG methylation status of 4 genes (p14^ARF, p16^INK4a, DAPK, and CDH1) in 510 subjects without gastric cancer. Helicobacter pylori (HP) infection status was determined by the rapid urease test, urea breath test, speculum examination, or serum antibody test. We determined the DNMT3A genotype using polymerase chain reaction single-strand conformation polymorphism (PCR-SSCP). CpG methylation status was determined by methylation-specific polymerase chain reaction (MSP). When the methylated band was stronger than 10 ng/μL according to the DNA marker, we judged CpG island hypermethylation (CIHM) to be present. Associations between genotypes and susceptibilities were assessed by logistic regression analysis.</p><p><strong>Results: </strong>The minor allele frequencies of both polymorphisms (rs6733868 and rs13428812) were lower in the CpG methylated groups of each of the 4 genes (p14^ARF, p16^INK4a, DAPK, and CDH1). Using a dominant genetic model, rs6733868 was significantly associated with the hypermethylation of each gene, whereas rs13428812 was associated with the methylation of 3 genes (all except p14^ARF). When low-CIHM was defined as 1 or 2 CpG islands methylated and high-CIHM was defined as 3 or more CpG islands methylated, carrying the minor allele of rs6733868 was associated with both decreased low- and high-CIHM, and that of rs13428812 also was associated with a decrease. Comparing low-CIHM with high-CIHM, carrying the minor alleles of rs6733868 or rs13428812 was related to decreased susceptibility to high-CIHM. In HP-infected subjects, carrying the minor alleles of rs6733868 or rs13428812 had a significantly greater association with decreased susceptibility to high-CIHM.</p><p><strong>Conclusions: </strong>Our study indicates that polymorphisms of DNMT3A are associated with the accumulation of gene methylation in gastric mucosa. Carrying the minor alleles of rs6733868 or rs13428812 inhibits aberrant gene methylations, which are typically enhanced by HP infection.</p>","PeriodicalId":9015,"journal":{"name":"BMC Medical Genetics","volume":" ","pages":"205"},"PeriodicalIF":0.0,"publicationDate":"2020-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12881-020-01142-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38497095","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Genotype-phenotype correlation of HbH disease in northern Iraq.","authors":"Rawand P Shamoon,&nbsp;Ahmed K Yassin,&nbsp;Ranan K Polus,&nbsp;Mohamad D Ali","doi":"10.1186/s12881-020-01141-8","DOIUrl":"https://doi.org/10.1186/s12881-020-01141-8","url":null,"abstract":"<p><strong>Background: </strong>HbH disease results from dysfunction of three, less commonly two, α-globin genes through various combinations of deletion and non-deletion mutations. Characterization of the mutations and the underlying genotypes is fundamental for proper screening and prevention of thalassaemia in any region. The aim of this study was to explore the genetic arrangements of HbH disease and to correlate the genotypes with the clinical phenotypes.</p><p><strong>Methods: </strong>A total of 44 HbH disease patients were enrolled in this study. They were clinically and haematologically assessed. The patients were tested for 21 common α-globin gene mutations using multiplex PCR and reverse hybridization. According to the genotype, the patients were categorized into two separate sub-groups, deletion and non-deletion types HbH disease.</p><p><strong>Results: </strong>Within the studied HbH disease patients, eight different α-globin gene mutations were detected in nine different genetic arrangements. The --^MED and -α^3.7 deletions were the two most frequently encountered mutations (37.5 and 35.2% respectively). Patients with deletion genotypes constituted 70.4%. The most common detected genotype was --^MED/-α^3.7 (59.1%), followed by α^poly-A1α/α^poly-A1α (13.6%). For the first time, coinheritance of two relatively mild mutations (-α^3.7/αα^Adana) was unpredictably detected in a 1.5 year-old child with Hb of 7.1 g/dL.</p><p><strong>Conclusion: </strong>The HbH disease patients' clinical characteristics were variable with no ample difference between the deletion and non-deletion types. These results can be of benefit for the screening and management of thalassaemia in this region.</p>","PeriodicalId":9015,"journal":{"name":"BMC Medical Genetics","volume":" ","pages":"203"},"PeriodicalIF":0.0,"publicationDate":"2020-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12881-020-01141-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38496516","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn's disease subjects.","authors":"Williams Turpin,&nbsp;Larbi Bedrani,&nbsp;Osvaldo Espin-Garcia,&nbsp;Wei Xu,&nbsp;Mark S Silverberg,&nbsp;Michelle I Smith,&nbsp;Juan Antonio Raygoza Garay,&nbsp;Sun-Ho Lee,&nbsp;David S Guttman,&nbsp;Anne Griffiths,&nbsp;Paul Moayyedi,&nbsp;Remo Panaccione,&nbsp;Hien Huynh,&nbsp;Hillary A Steinhart,&nbsp;Guy Aumais,&nbsp;Levinus A Dieleman,&nbsp;Dan Turner,&nbsp;Andrew D Paterson,&nbsp;Kenneth Croitoru","doi":"10.1186/s12881-020-01115-w","DOIUrl":"https://doi.org/10.1186/s12881-020-01115-w","url":null,"abstract":"<p><strong>Background: </strong>Genetic analyses have identified many variants associated with the risk of inflammatory bowel disease (IBD) development. Among these variants, the ones located within the NOD2 gene have the highest odds ratio of all IBD genetic risk variants. Also, patients with Crohn's disease (CD) have been shown to have an altered gut microbiome, which might be a reflection of inflammation itself or an effect of other parameters that contribute to the risk of the disease. Since NOD2 is an intracellular pattern recognition receptor that senses bacterial peptidoglycan in the cytosol and stimulates the host immune response (Al Nabhani et al., PLoS Pathog 13:e1006177, 2017), it is hypothesized that NOD2 variants represent perfect candidates for influencing host-microbiome interactions. We hypothesized that NOD2 risk variants affect the microbiome composition of healthy first degree relative (FDR) of CD patients and thus potentially contribute to an altered microbiome state before disease onset.</p><p><strong>Methods: </strong>Based on this, we studied a large cohort of 1546 healthy FDR of CD patients and performed a focused analysis of the association of three major CD SNPs in the coding region of the NOD2 gene, which are known to confer a 15-40-fold increased risk of developing CD in homozygous or compound heterozygous individuals.</p><p><strong>Results: </strong>Our results show that carriers of the C allele at rs2066845 was significantly associated with an increase in relative abundance in the fecal bacterial family Erysipelotrichaceae.</p><p><strong>Conclusions: </strong>This result suggests that NOD2 polymorphisms contribute to fecal microbiome composition in asymptomatic individuals. Whether this modulation of the microbiome influences the future development of CD remains to be assessed.</p>","PeriodicalId":9015,"journal":{"name":"BMC Medical Genetics","volume":" ","pages":"204"},"PeriodicalIF":0.0,"publicationDate":"2020-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12881-020-01115-w","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38493912","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"KANK1-NTRK3 fusions define a subset of BRAF mutation negative renal metanephric adenomas.","authors":"Aida Catic,&nbsp;Amina Kurtovic-Kozaric,&nbsp;Ardis Sophian,&nbsp;Lech Mazur,&nbsp;Faruk Skenderi,&nbsp;Ondrej Hes,&nbsp;Stephen Rohan,&nbsp;Dinesh Rakheja,&nbsp;Jillene Kogan,&nbsp;Michael R Pins","doi":"10.1186/s12881-020-01143-6","DOIUrl":"https://doi.org/10.1186/s12881-020-01143-6","url":null,"abstract":"<p><strong>Background: </strong>Metanephric adenoma (MA) is a rare benign renal neoplasm. On occasion, MA can be difficult to differentiate from renal malignancies such as papillary renal cell carcinoma in adults and Wilms̕ tumor in children. Despite recent advancements in tumor genomics, there is limited data available regarding the genetic alterations characteristic of MA. The purpose of this study is to determine the frequency of metanephric adenoma cases exhibiting cytogenetic aberration t (9;15)(p24;q24), and to investigate the association between t (9,15) and BRAF mutation in metanephric adenoma.</p><p><strong>Methods: </strong>This study was conducted on 28 archival formalin fixed paraffin-embedded (FFPE) specimens from patients with pathologically confirmed MA. Tissue blocks were selected for BRAF sequencing and fluorescent in situ hybridization (FISH) analysis for chromosomal rearrangement between KANK1 on chromosome 9 (9p24.3) and NTRK3 on chromosome 15 (15q25.3), which was previously characterized and described in two MA cases.</p><p><strong>Results: </strong>BRAF^V600E mutation was identified in 62% of our cases, 9 (38%) cases were BRAF^WT, and 4 cases were uninformative. Of the 20 tumors with FISH results, two (10%) were positive for KANK1-NTRK3 fusion. Both cases were BRAF^WT suggesting mutual exclusivity of BRAF^V600E and KANK1-NTRK3 fusion, the first such observation in the literature.</p><p><strong>Conclusions: </strong>Our data shows that BRAF mutation in MA may not be as frequent as suggested in the literature and KANK-NTRK3 fusions may account for a subset of BRAF^WT cases in younger patients. FISH analysis for KANK1-NTRK3 fusion or conventional cytogenetic analysis may be warranted to establish the diagnosis of MA in morphologically and immunohistochemically ambiguous MA cases lacking BRAF mutations.</p>","PeriodicalId":9015,"journal":{"name":"BMC Medical Genetics","volume":" ","pages":"202"},"PeriodicalIF":0.0,"publicationDate":"2020-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12881-020-01143-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38479503","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Pathogenic NF1 truncating mutation and copy number alterations in a dedifferentiated liposarcoma with multiple lung metastasis: a case report.","authors":"Yoon-Seob Kim,&nbsp;Sun Shin,&nbsp;Seung-Hyun Jung,&nbsp;Yeun-Jun Chung","doi":"10.1186/s12881-020-01137-4","DOIUrl":"https://doi.org/10.1186/s12881-020-01137-4","url":null,"abstract":"<p><strong>Background: </strong>Dedifferentiated liposarcoma (DDLPS), which accounts for an estimated 15-20% of liposarcomas, is a high-grade and aggressive malignant neoplasm, exhibiting a poor response to available therapeutic agents. However, genetic alteration profiles of DDLPS as well as the role of NF1 mutations have not been studied extensively.</p><p><strong>Case presentation: </strong>The current study reports a patient presenting with rapidly growing DDLPS accompanied by multiple lung and pleural metastases, in whom whole-exome sequencing revealed a NF1 truncating mutation of the known pathogenic variant, c.C7486T, p.R2496X, as well as multiple copy number alterations (CNAs), including the well-known 12q13-15 amplification, and multiple chromothripsis events encompassing potential cancer-related genes.</p><p><strong>Conclusions: </strong>Our results suggest that, in addition to the 12q13-15 amplification, NF1 inactivation mutation and other CNAs may contribute to DDLPS tumorigenesis accompanied by aggressive clinical features.</p>","PeriodicalId":9015,"journal":{"name":"BMC Medical Genetics","volume":" ","pages":"200"},"PeriodicalIF":0.0,"publicationDate":"2020-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12881-020-01137-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38480595","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Influence of MIF polymorphisms on CpG island hyper-methylation of CDKN2A in the patients with ulcerative colitis.","authors":"Naoko Sakurai,&nbsp;Tomoyuki Shibata,&nbsp;Masakatsu Nakamura,&nbsp;Hikaru Takano,&nbsp;Tasuku Hayashi,&nbsp;Masafumi Ota,&nbsp;Tomoe Nomura-Horita,&nbsp;Ranji Hayashi,&nbsp;Takeo Shimasaki,&nbsp;Toshimi Ostuka,&nbsp;Tomomitsu Tahara,&nbsp;Tomiyasu Arisawa","doi":"10.1186/s12881-020-01140-9","DOIUrl":"https://doi.org/10.1186/s12881-020-01140-9","url":null,"abstract":"<p><strong>Background: </strong>CDKN2A hypermethylation is among the major events associated with carcinogenesis and is also observed in non-neoplastic colonic mucosa in patients with ulcerative colitis (UC). Macrophage migration inhibitory factor (MIF) plays a crucial role in promoting gastrointestinal inflammation characteristic of UC. The aim of this study is to explore associations between CDKN2A methylation status and MIF polymorphisms (rs755622 and rs5844572).</p><p><strong>Methods: </strong>One hundred and fifty-nine patients diagnosed with UC were enrolled in this study. The methylation status of p14^ARF and p16^INK4a was determined by MSP; MIF genotypes were identified by PCR-SSCP.</p><p><strong>Results: </strong>We found no differences with respect to mean age, gender, clinical type (chronic continuous or relapse/remitting), or extent of disease among the patients with methylated and unmethylated p14^ARF or p16^INK4a. Carrying the rs755622 C allele indicated a significantly higher risk for p14^ARF methylation (odds ratio (OR), 2.16; 95% confidence interval (CI), 1.08-4.32; p = 0.030); similarly, carrying the rs5844572 7-repeat allele indicated a significantly higher risk for p16^INK4a methylation (OR, 2.57; 95% CI, 1.26-5.24; p = 0.0094) after an adjusted regression analysis. The carriers of the rs755662 C allele or the rs5844572 7-repeat allele were both at a significantly higher risk for methylation of both p14^ARF and p16^INK4a when compared to the cohort in which neither of the genes were methylated (OR, 2.70; 95% CI, 1.22-6.01; p = 0.015 and OR, 2.87; 95% CI, 1.25-6.62; p = 0.013, respectively). Additionally, carrying rs755622 C allele was significantly associated with CIHM in chronic continuous of clinical type and total colitis (OR, 25.9; 95% CI, 2.55-262.6; p = 0.0059 and OR, 4.38; 95% CI, 1.12-17.2; p = 0.034, respectively), and carrying 7-repeat allele of rs5844572 was significantly associated in chronic continuous type (OR, 14.5; 95%CI, 1.46-144.3; p = 0.022).</p><p><strong>Conclusions: </strong>Taken together, our findings suggest that MIF genotypes associated with inflammation may also be involved in promoting carcinogenesis via CDKN2A hypermethylation in patients diagnosed with UC.</p>","PeriodicalId":9015,"journal":{"name":"BMC Medical Genetics","volume":" ","pages":"201"},"PeriodicalIF":0.0,"publicationDate":"2020-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12881-020-01140-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38575796","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}