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  1. AU="Kenan Onel"
  2. AU="Lawrence, Marc R"
  3. AU="Zeiler, Frederick A"
  4. AU="de la Cueva, Pablo"
  5. AU="Fuh, Jerry Ying Hsi"
  6. AU="Park, Adrian J"
  7. AU="Joshi, K D"

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  1. Article ; Online: Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma.

    Imge Hulur / Andrew D Skol / Eric R Gamazon / Nancy J Cox / Kenan Onel

    PLoS ONE, Vol 12, Iss 10, p e

    2017  Volume 0185730

    Abstract: Melanoma is the deadliest form of skin cancer and presents a significant health care burden in many countries. In addition to ultraviolet radiation in sunlight, the main causal factor for melanoma, genetic factors also play an important role in melanoma ... ...

    Abstract Melanoma is the deadliest form of skin cancer and presents a significant health care burden in many countries. In addition to ultraviolet radiation in sunlight, the main causal factor for melanoma, genetic factors also play an important role in melanoma susceptibility. Although genome-wide association studies have identified many single nucleotide polymorphisms associated with melanoma, little is known about the proportion of disease risk attributable to these loci and their distribution throughout the genome. Here, we investigated the genetic architecture of melanoma in 1,888 cases and 990 controls of European non-Hispanic ancestry. We estimated the overall narrow-sense heritability of melanoma to be 0.18 (P < 0.03), indicating that genetics contributes significantly to the risk of sporadically-occurring melanoma. We then demonstrated that only a small proportion of this risk is attributable to known risk variants, suggesting that much remains unknown of the role of genetics in melanoma. To investigate further the genetic architecture of melanoma, we partitioned the heritability by chromosome, minor allele frequency, and functional annotations. We showed that common genetic variation contributes significantly to melanoma risk, with a risk model defined by a handful of genomic regions rather than many risk loci distributed throughout the genome. We also demonstrated that variants affecting gene expression in skin account for a significant proportion of the heritability, and are enriched among melanoma risk loci. Finally, by incorporating skin color into our analyses, we observed both a shift in significance for melanoma-associated loci and an enrichment of expression quantitative trait loci among melanoma susceptibility variants. These findings suggest that skin color may be an important modifier of melanoma risk. We speculate that incorporating skin color and other non-genetic factors into genetic studies may allow for an improved understanding of melanoma susceptibility and guide future investigations to ...
    Keywords Medicine ; R ; Science ; Q
    Subject code 570
    Language English
    Publishing date 2017-01-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: Genetically Raised Circulating Bilirubin Levels and Risk of Ten Cancers

    Nazlisadat Seyed Khoei / Robert Carreras-Torres / Neil Murphy / Marc J. Gunter / Paul Brennan / Karl Smith-Byrne / Daniela Mariosa / James Mckay / Tracy A. O’Mara / Ruth Jarrett / Henrik Hjalgrim / Karin E. Smedby / Wendy Cozen / Kenan Onel / Arjan Diepstra / Karl-Heinz Wagner / Heinz Freisling

    Cells, Vol 10, Iss 394, p

    A Mendelian Randomization Study

    2021  Volume 394

    Abstract: Bilirubin, an endogenous antioxidant, may play a protective role in cancer development. We applied two-sample Mendelian randomization to investigate whether genetically raised bilirubin levels are causally associated with the risk of ten cancers ( ... ...

    Abstract Bilirubin, an endogenous antioxidant, may play a protective role in cancer development. We applied two-sample Mendelian randomization to investigate whether genetically raised bilirubin levels are causally associated with the risk of ten cancers (pancreas, kidney, endometrium, ovary, breast, prostate, lung, Hodgkin’s lymphoma, melanoma, and neuroblastoma). The number of cases and their matched controls of European descent ranged from 122,977 and 105,974 for breast cancer to 1200 and 6417 for Hodgkin’s lymphoma, respectively. A total of 115 single-nucleotide polymorphisms (SNPs) associated ( p < 5 × 10 −8 ) with circulating total bilirubin, extracted from a genome-wide association study in the UK Biobank, were used as instrumental variables. One SNP (rs6431625) in the promoter region of the uridine-diphosphoglucuronate glucuronosyltransferase1A1 ( UGT1A1) gene explained 16.9% and the remaining 114 SNPs (non- UGT1A1 SNPs) explained 3.1% of phenotypic variance in circulating bilirubin levels. A one-standarddeviation increment in circulating bilirubin (≈ 4.4 µmol/L), predicted by non- UGT1A1 SNPs, was inversely associated with risk of squamous cell lung cancer and Hodgkin’s lymphoma (odds ratio (OR) 0.85, 95% confidence interval (CI) 0.73–0.99, P 0.04 and OR 0.64, 95% CI 0.42–0.99, p 0.04, respectively), which was confirmed after removing potential pleiotropic SNPs. In contrast, a positive association was observed with the risk of breast cancer after removing potential pleiotropic SNPs (OR 1.12, 95% CI 1.04–1.20, p 0.002). There was little evidence for robust associations with the other seven cancers investigated. Genetically raised bilirubin levels were inversely associated with risk of squamous cell lung cancer as well as Hodgkin’s lymphoma and positively associated with risk of breast cancer. Further studies are required to investigate the utility of bilirubin as a low-cost clinical marker to improve risk prediction for certain cancers.
    Keywords bilirubin ; UGT1A1 ; Mendelian randomization ; cancer risk ; Biology (General) ; QH301-705.5
    Subject code 610 ; 616
    Language English
    Publishing date 2021-02-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: ExScalibur

    Riyue Bao / Kyle Hernandez / Lei Huang / Wenjun Kang / Elizabeth Bartom / Kenan Onel / Samuel Volchenboum / Jorge Andrade

    PLoS ONE, Vol 10, Iss 8, p e

    A High-Performance Cloud-Enabled Suite for Whole Exome Germline and Somatic Mutation Identification.

    2015  Volume 0135800

    Abstract: Whole exome sequencing has facilitated the discovery of causal genetic variants associated with human diseases at deep coverage and low cost. In particular, the detection of somatic mutations from tumor/normal pairs has provided insights into the cancer ... ...

    Abstract Whole exome sequencing has facilitated the discovery of causal genetic variants associated with human diseases at deep coverage and low cost. In particular, the detection of somatic mutations from tumor/normal pairs has provided insights into the cancer genome. Although there is an abundance of publicly-available software for the detection of germline and somatic variants, concordance is generally limited among variant callers and alignment algorithms. Successful integration of variants detected by multiple methods requires in-depth knowledge of the software, access to high-performance computing resources, and advanced programming techniques. We present ExScalibur, a set of fully automated, highly scalable and modulated pipelines for whole exome data analysis. The suite integrates multiple alignment and variant calling algorithms for the accurate detection of germline and somatic mutations with close to 99% sensitivity and specificity. ExScalibur implements streamlined execution of analytical modules, real-time monitoring of pipeline progress, robust handling of errors and intuitive documentation that allows for increased reproducibility and sharing of results and workflows. It runs on local computers, high-performance computing clusters and cloud environments. In addition, we provide a data analysis report utility to facilitate visualization of the results that offers interactive exploration of quality control files, read alignment and variant calls, assisting downstream customization of potential disease-causing mutations. ExScalibur is open-source and is also available as a public image on Amazon cloud.
    Keywords Medicine ; R ; Science ; Q
    Subject code 004
    Language English
    Publishing date 2015-01-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article ; Online: Biallelic TET2 mutations confer sensitivity to 5′-azacitidine in acute myeloid leukemia

    Friedrich Stölzel / Sarah E. Fordham / Devi Nandana / Wei-Yu Lin / Helen Blair / Claire Elstob / Hayden L. Bell / Brigitte Mohr / Leo Ruhnke / Desiree Kunadt / Claudia Dill / Daniel Allsop / Rachel Piddock / Emmanouela-Niki Soura / Catherine Park / Mohd Fadly / Thahira Rahman / Abrar Alharbi / Manja Wobus /
    Heidi Altmann / Christoph Röllig / Lisa Wagenführ / Gail L. Jones / Tobias Menne / Graham H. Jackson / Helen J. Marr / Jude Fitzgibbon / Kenan Onel / Manja Meggendorfer / Amber Robinson / Zuzanna Bziuk / Emily Bowes / Olaf Heidenreich / Torsten Haferlach / Sara Villar / Beñat Ariceta / Rosa Ayala Diaz / Steven J. Altschuler / Lani F. Wu / Felipe Prosper / Pau Montesinos / Joaquin Martinez-Lopez / Martin Bornhäuser / James M. Allan

    JCI Insight, Vol 8, Iss

    2023  Volume 2

    Abstract: Precision medicine can significantly improve outcomes for patients with cancer, but implementation requires comprehensive characterization of tumor cells to identify therapeutically exploitable vulnerabilities. Here, we describe somatic biallelic TET2 ... ...

    Abstract Precision medicine can significantly improve outcomes for patients with cancer, but implementation requires comprehensive characterization of tumor cells to identify therapeutically exploitable vulnerabilities. Here, we describe somatic biallelic TET2 mutations in an elderly patient with acute myeloid leukemia (AML) that was chemoresistant to anthracycline and cytarabine but acutely sensitive to 5′-azacitidine (5′-Aza) hypomethylating monotherapy, resulting in long-term morphological remission. Given the role of TET2 as a regulator of genomic methylation, we hypothesized that mutant TET2 allele dosage affects response to 5′-Aza. Using an isogenic cell model system and an orthotopic mouse xenograft, we demonstrate that biallelic TET2 mutations confer sensitivity to 5′-Aza compared with cells with monoallelic mutations. Our data argue in favor of using hypomethylating agents for chemoresistant disease or as first-line therapy in patients with biallelic TET2-mutated AML and demonstrate the importance of considering mutant allele dosage in the implementation of precision medicine for patients with cancer.
    Keywords Hematology ; Medicine ; R
    Subject code 610
    Language English
    Publishing date 2023-01-01T00:00:00Z
    Publisher American Society for Clinical investigation
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article ; Online: A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology

    Eric A. Hungate / Sapana R. Vora / Eric R. Gamazon / Takaya Moriyama / Timothy Best / Imge Hulur / Younghee Lee / Tiffany-Jane Evans / Eva Ellinghaus / Martin Stanulla / Jéremie Rudant / Laurent Orsi / Jacqueline Clavel / Elizabeth Milne / Rodney J. Scott / Ching-Hon Pui / Nancy J. Cox / Mignon L. Loh / Jun J. Yang /
    Andrew D. Skol / Kenan Onel

    Nature Communications, Vol 7, Iss 1, Pp 1-

    2016  Volume 11

    Abstract: A risk variant located at 9p21.3 is associated with cancer risk in pediatric B-cell precursor acute lymphoblastic leukaemia. Here, the authors show that this variant affects the gene expression of the tumour suppressor gene Cdkn2b. ...

    Abstract A risk variant located at 9p21.3 is associated with cancer risk in pediatric B-cell precursor acute lymphoblastic leukaemia. Here, the authors show that this variant affects the gene expression of the tumour suppressor gene Cdkn2b.
    Keywords Science ; Q
    Language English
    Publishing date 2016-02-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article ; Online: Author Correction

    Wei-Yu Lin / Sarah E. Fordham / Eric Hungate / Nicola J. Sunter / Claire Elstob / Yaobo Xu / Catherine Park / Anne Quante / Konstantin Strauch / Christian Gieger / Andrew Skol / Thahira Rahman / Lara Sucheston-Campbell / Junke Wang / Theresa Hahn / Alyssa I. Clay-Gilmour / Gail L. Jones / Helen J. Marr / Graham H. Jackson /
    Tobias Menne / Mathew Collin / Adam Ivey / Robert K. Hills / Alan K. Burnett / Nigel H. Russell / Jude Fitzgibbon / Richard A. Larson / Michelle M. Le Beau / Wendy Stock / Olaf Heidenreich / Abrar Alharbi / David J. Allsup / Richard S. Houlston / Jean Norden / Anne M. Dickinson / Elisabeth Douglas / Clare Lendrem / Ann K. Daly / Louise Palm / Kim Piechocki / Sally Jeffries / Martin Bornhäuser / Christoph Röllig / Heidi Altmann / Leo Ruhnke / Desiree Kunadt / Lisa Wagenführ / Heather J. Cordell / Rebecca Darlay / Mette K. Andersen / Maria C. Fontana / Giovanni Martinelli / Giovanni Marconi / Miguel A. Sanz / José Cervera / Inés Gómez-Seguí / Thomas Cluzeau / Chimène Moreilhon / Sophie Raynaud / Heinz Sill / Maria Teresa Voso / Francesco Lo-Coco / Hervé Dombret / Meyling Cheok / Claude Preudhomme / Rosemary E. Gale / David Linch / Julia Gaal-Wesinger / Andras Masszi / Daniel Nowak / Wolf-Karsten Hofmann / Amanda Gilkes / Kimmo Porkka / Jelena D. Milosevic Feenstra / Robert Kralovics / David Grimwade / Manja Meggendorfer / Torsten Haferlach / Szilvia Krizsán / Csaba Bödör / Friedrich Stölzel / Kenan Onel / James M. Allan

    Nature Communications, Vol 13, Iss 1, Pp 1-

    Genome-wide association study identifies susceptibility loci for acute myeloid leukemia

    2022  Volume 1

    Keywords Science ; Q
    Language English
    Publishing date 2022-01-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article ; Online: Correction

    Yi-Hung Carol Tan / Soundararajan Krishnaswamy / Suvobroto Nandi / Rajani Kanteti / Sapana Vora / Kenan Onel / Rifat Hasina / Fang-Yi Lo / Essam El-Hashani / Gustavo Cervantes / Matthew Robinson / Han-Shui Hsu / Stephen C. Kales / Stanley Lipkowitz / Theodore Karrison / Martin Sattler / Everett E. Vokes / Yi-Ching Wang / Ravi Salgia

    PLoS ONE, Vol 6, Iss

    CBL Is Frequently Altered in Lung Cancers: Its Relationship to Mutations in MET and EGFR Tyrosine Kinases.

    2011  Volume 1

    Keywords Medicine ; R ; Science ; Q
    Language English
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article ; Online: Correction

    Yi-Hung Carol Tan / Soundararajan Krishnaswamy / Suvobroto Nandi / Rajani Kanteti / Sapana Vora / Kenan Onel / Rifat Hasina / Fang-Yi Lo / Essam El-Hashani / Gustavo Cervantes / Matthew Robinson / Han-Shui Hsu / Stephen C. Kales / Stanley Lipkowitz / Theodore Karrison / Martin Sattler / Everett E. Vokes / Yi-Ching Wang / Ravi Salgia

    PLoS ONE, Vol 6, Iss

    CBL Is Frequently Altered in Lung Cancers: Its Relationship to Mutations in MET and EGFR Tyrosine Kinases

    2011  Volume 1

    Keywords Medicine ; R ; Science ; Q
    Language English
    Publishing date 2011-01-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article ; Online: CBL is frequently altered in lung cancers

    Yi-Hung Carol Tan / Soundararajan Krishnaswamy / Suvobroto Nandi / Rajani Kanteti / Sapana Vora / Kenan Onel / Rifat Hasina / Fang-Yi Lo / Essam El-Hashani / Gustavo Cervantes / Matthew Robinson / Han-Shui Hsu / Stephen C Kales / Stanley Lipkowitz / Theodore Karrison / Martin Sattler / Everett E Vokes / Yi-Ching Wang / Ravi Salgia

    PLoS ONE, Vol 5, Iss 1, p e

    its relationship to mutations in MET and EGFR tyrosine kinases.

    2010  Volume 8972

    Abstract: Non-small cell lung cancer (NSCLC) is a heterogeneous group of disorders with a number of genetic and proteomic alterations. c-CBL is an E3 ubiquitin ligase and adaptor molecule important in normal homeostasis and cancer. We determined the genetic ... ...

    Abstract Non-small cell lung cancer (NSCLC) is a heterogeneous group of disorders with a number of genetic and proteomic alterations. c-CBL is an E3 ubiquitin ligase and adaptor molecule important in normal homeostasis and cancer. We determined the genetic variations of c-CBL, relationship to receptor tyrosine kinases (EGFR and MET), and functionality in NSCLC.Using archival formalin-fixed paraffin embedded (FFPE) extracted genomic DNA, we show that c-CBL mutations occur in somatic fashion for lung cancers. c-CBL mutations were not mutually exclusive of MET or EGFR mutations; however they were independent of p53 and KRAS mutations. In normal/tumor pairwise analysis, there was significant loss of heterozygosity (LOH) for the c-CBL locus (22%, n = 8/37) and none of these samples revealed any mutation in the remaining copy of c-CBL. The c-CBL LOH also positively correlated with EGFR and MET mutations observed in the same samples. Using select c-CBL somatic mutations such as S80N/H94Y, Q249E and W802* (obtained from Caucasian, Taiwanese and African-American samples, respectively) transfected in NSCLC cell lines, there was increased cell viability and cell motility.Taking the overall mutation rate of c-CBL to be a combination as somatic missense mutation and LOH, it is clear that c-CBL is highly mutated in lung cancers and may play an essential role in lung tumorigenesis and metastasis.
    Keywords Medicine ; R ; Science ; Q
    Subject code 616
    Language English
    Publishing date 2010-01-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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