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  1. Article ; Online: An enhanced genetic model of colorectal cancer progression history

    Lixing Yang / Su Wang / Jake June-Koo Lee / Semin Lee / Eunjung Lee / Eve Shinbrot / David A. Wheeler / Raju Kucherlapati / Peter J. Park

    Genome Biology, Vol 20, Iss 1, Pp 1-

    2019  Volume 17

    Abstract: Abstract Background The classical genetic model of colorectal cancer presents APC mutations as the earliest genomic alterations, followed by KRAS and TP53 mutations. However, the timing and relative order of clonal expansion and other types of genomic ... ...

    Abstract Abstract Background The classical genetic model of colorectal cancer presents APC mutations as the earliest genomic alterations, followed by KRAS and TP53 mutations. However, the timing and relative order of clonal expansion and other types of genomic alterations, such as genomic rearrangements, are still unclear. Results Here, we perform comprehensive bioinformatic analysis to dissect the relative timing of somatic genetic alterations in 63 colorectal cancers with whole-genome sequencing data. Utilizing allele fractions of somatic single nucleotide variants as molecular clocks while accounting for the presence of copy number changes and structural alterations, we identify key events in the evolution of colorectal tumors. We find that driver point mutations, gene fusions, and arm-level copy losses typically arise early in tumorigenesis; different mechanisms act on distinct genomic regions to drive DNA copy changes; and chromothripsis—clustered rearrangements previously thought to occur as a single catastrophic event—is frequent and may occur multiple times independently in the same tumor through different mechanisms. Furthermore, our computational approach reveals that, in contrast to recent studies, selection is often present on subclones and that multiple evolutionary models can operate in a single tumor at different stages. Conclusion Combining these results, we present a refined tumor progression model which significantly expands our understanding of the tumorigenic process of human colorectal cancer.
    Keywords Tumor evolution ; Tumor heterogeneity ; Aneuploidy ; Kataegis ; Biology (General) ; QH301-705.5 ; Genetics ; QH426-470
    Language English
    Publishing date 2019-08-01T00:00:00Z
    Publisher BMC
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: Morphological Detection of Plasma Membrane Changes During Apoptosis Using Enhanced Green Fluorescent Protein

    Eve Shinbrot / Collin M. Spencer / Steven R. Kain

    BioTechniques, Vol 26, Iss 6, Pp 1064-

    1999  Volume 1068

    Keywords Biology (General) ; QH301-705.5
    Language English
    Publishing date 1999-06-01T00:00:00Z
    Publisher Future Science Ltd
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article: Mutational Strand Asymmetries in Cancer Genomes Reveal Mechanisms of DNA Damage and Repair

    Haradhvala, Nicholas J / Paz Polak / Petar Stojanov / Kyle R. Covington / Eve Shinbrot / Julian M. Hess / Esther Rheinbay / Jaegil Kim / Yosef E. Maruvka / Lior Z. Braunstein / Atanas Kamburov / Philip C. Hanawalt / David A. Wheeler / Amnon Koren / Michael S. Lawrence / Gad Getz

    Cell. 2016 Jan. 28, v. 164

    2016  

    Abstract: Mutational processes constantly shape the somatic genome, leading to immunity, aging, cancer, and other diseases. When cancer is the outcome, we are afforded a glimpse into these processes by the clonal expansion of the malignant cell. Here, we ... ...

    Abstract Mutational processes constantly shape the somatic genome, leading to immunity, aging, cancer, and other diseases. When cancer is the outcome, we are afforded a glimpse into these processes by the clonal expansion of the malignant cell. Here, we characterize a less explored layer of the mutational landscape of cancer: mutational asymmetries between the two DNA strands. Analyzing whole-genome sequences of 590 tumors from 14 different cancer types, we reveal widespread asymmetries across mutagenic processes, with transcriptional (“T-class”) asymmetry dominating UV-, smoking-, and liver-cancer-associated mutations and replicative (“R-class”) asymmetry dominating POLE-, APOBEC-, and MSI-associated mutations. We report a striking phenomenon of transcription-coupled damage (TCD) on the non-transcribed DNA strand and provide evidence that APOBEC mutagenesis occurs on the lagging-strand template during DNA replication. As more genomes are sequenced, studying and classifying their asymmetries will illuminate the underlying biological mechanisms of DNA damage and repair.
    Keywords DNA ; DNA repair ; DNA replication ; genome ; immunity ; mutagenesis ; mutagenicity ; neoplasms ; transcription (genetics)
    Language English
    Dates of publication 2016-0128
    Size p. 538-549.
    Publishing place Elsevier Inc.
    Document type Article
    ZDB-ID 187009-9
    ISSN 1097-4172 ; 0092-8674
    ISSN (online) 1097-4172
    ISSN 0092-8674
    DOI 10.1016/j.cell.2015.12.050
    Database NAL-Catalogue (AGRICOLA)

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  4. Article ; Online: Genomic and Molecular Landscape of DNA Damage Repair Deficiency across The Cancer Genome Atlas

    Theo A. Knijnenburg / Linghua Wang / Michael T. Zimmermann / Nyasha Chambwe / Galen F. Gao / Andrew D. Cherniack / Huihui Fan / Hui Shen / Gregory P. Way / Casey S. Greene / Yuexin Liu / Rehan Akbani / Bin Feng / Lawrence A. Donehower / Chase Miller / Yang Shen / Mostafa Karimi / Haoran Chen / Pora Kim /
    Peilin Jia / Eve Shinbrot / Shaojun Zhang / Jianfang Liu / Hai Hu / Matthew H. Bailey / Christina Yau / Denise Wolf / Zhongming Zhao / John N. Weinstein / Lei Li / Li Ding / Gordon B. Mills / Peter W. Laird / David A. Wheeler / Ilya Shmulevich / Raymond J. Monnat, Jr. / Yonghong Xiao / Chen Wang / Samantha J. Caesar-Johnson / John A. Demchok / Ina Felau / Melpomeni Kasapi / Martin L. Ferguson / Carolyn M. Hutter / Heidi J. Sofia / Roy Tarnuzzer / Zhining Wang / Liming Yang / Jean C. Zenklusen / Jiashan (Julia) Zhang

    Cell Reports, Vol 23, Iss 1, Pp 239-254.e

    2018  Volume 6

    Abstract: Summary: DNA damage repair (DDR) pathways modulate cancer risk, progression, and therapeutic response. We systematically analyzed somatic alterations to provide a comprehensive view of DDR deficiency across 33 cancer types. Mutations with accompanying ... ...

    Abstract Summary: DNA damage repair (DDR) pathways modulate cancer risk, progression, and therapeutic response. We systematically analyzed somatic alterations to provide a comprehensive view of DDR deficiency across 33 cancer types. Mutations with accompanying loss of heterozygosity were observed in over 1/3 of DDR genes, including TP53 and BRCA1/2. Other prevalent alterations included epigenetic silencing of the direct repair genes EXO5, MGMT, and ALKBH3 in ∼20% of samples. Homologous recombination deficiency (HRD) was present at varying frequency in many cancer types, most notably ovarian cancer. However, in contrast to ovarian cancer, HRD was associated with worse outcomes in several other cancers. Protein structure-based analyses allowed us to predict functional consequences of rare, recurrent DDR mutations. A new machine-learning-based classifier developed from gene expression data allowed us to identify alterations that phenocopy deleterious TP53 mutations. These frequent DDR gene alterations in many human cancers have functional consequences that may determine cancer progression and guide therapy. : Knijnenburg et al. present The Cancer Genome Atlas (TCGA) Pan-Cancer analysis of DNA damage repair (DDR) deficiency in cancer. They use integrative genomic and molecular analyses to identify frequent DDR alterations across 33 cancer types, correlate gene- and pathway-level alterations with genome-wide measures of genome instability and impaired function, and demonstrate the prognostic utility of DDR deficiency scores. Keywords: The Cancer Genome Atlas PanCanAtlas project, DNA damage repair, somatic mutations, somatic copy-number alterations, epigenetic silencing, DNA damage footprints, mutational signatures, integrative statistical analysis, protein structure analysis
    Keywords Biology (General) ; QH301-705.5
    Subject code 616
    Language English
    Publishing date 2018-04-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article ; Online: Landscape of somatic single nucleotide variants and indels in colorectal cancer and impact on survival

    Syed H. Zaidi / Tabitha A. Harrison / Amanda I. Phipps / Robert Steinfelder / Quang M. Trinh / Conghui Qu / Barbara L. Banbury / Peter Georgeson / Catherine S. Grasso / Marios Giannakis / Jeremy B. Adams / Elizabeth Alwers / Efrat L. Amitay / Richard T. Barfield / Sonja I. Berndt / Ivan Borozan / Hermann Brenner / Stefanie Brezina / Daniel D. Buchanan /
    Yin Cao / Andrew T. Chan / Jenny Chang-Claude / Charles M. Connolly / David A. Drew / Alton Brad Farris / Jane C. Figueiredo / Amy J. French / Charles S. Fuchs / Levi A. Garraway / Steve Gruber / Mark A. Guinter / Stanley R. Hamilton / Sophia Harlid / Lawrence E. Heisler / Akihisa Hidaka / John L. Hopper / Wen-Yi Huang / Jeroen R. Huyghe / Mark A. Jenkins / Paul M. Krzyzanowski / Mathieu Lemire / Yi Lin / Xuemei Luo / Elaine R. Mardis / John D. McPherson / Jessica K. Miller / Victor Moreno / Xinmeng Jasmine Mu / Reiko Nishihara / Nickolas Papadopoulos / Danielle Pasternack / Michael J. Quist / Adilya Rafikova / Emma E. G. Reid / Eve Shinbrot / Brian H. Shirts / Lincoln D. Stein / Cherie D. Teney / Lee Timms / Caroline Y. Um / Bethany Van Guelpen / Megan Van Tassel / Xiaolong Wang / David A. Wheeler / Christina K. Yung / Li Hsu / Shuji Ogino / Andrea Gsur / Polly A. Newcomb / Steven Gallinger / Michael Hoffmeister / Peter T. Campbell / Stephen N. Thibodeau / Wei Sun / Thomas J. Hudson / Ulrike Peters

    Nature Communications, Vol 11, Iss 1, Pp 1-

    2020  Volume 12

    Abstract: Large scale sequencing study is of paramount importance to unravel the heterogeneity of colorectal cancer. Here, the authors sequenced 205 cancer genes in more than 2000 tumours and identified additional mutated driver genes, determined that mutational ... ...

    Abstract Large scale sequencing study is of paramount importance to unravel the heterogeneity of colorectal cancer. Here, the authors sequenced 205 cancer genes in more than 2000 tumours and identified additional mutated driver genes, determined that mutational burden and specific mutations in TP53 are associated with survival odds.
    Keywords Science ; Q
    Language English
    Publishing date 2020-07-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article ; Online: Integrative Genomic Analysis of Cholangiocarcinoma Identifies Distinct IDH-Mutant Molecular Profiles

    Farshad Farshidfar / Siyuan Zheng / Marie-Claude Gingras / Yulia Newton / Juliann Shih / A. Gordon Robertson / Toshinori Hinoue / Katherine A. Hoadley / Ewan A. Gibb / Jason Roszik / Kyle R. Covington / Chia-Chin Wu / Eve Shinbrot / Nicolas Stransky / Apurva Hegde / Ju Dong Yang / Ed Reznik / Sara Sadeghi / Chandra Sekhar Pedamallu /
    Akinyemi I. Ojesina / Julian M. Hess / J. Todd Auman / Suhn K. Rhie / Reanne Bowlby / Mitesh J. Borad / Andrew X. Zhu / Josh M. Stuart / Chris Sander / Rehan Akbani / Andrew D. Cherniack / Vikram Deshpande / Taofic Mounajjed / Wai Chin Foo / Michael S. Torbenson / David E. Kleiner / Peter W. Laird / David A. Wheeler / Autumn J. McRee / Oliver F. Bathe / Jesper B. Andersen / Nabeel Bardeesy / Lewis R. Roberts / Lawrence N. Kwong

    Cell Reports, Vol 18, Iss 11, Pp 2780-

    2017  Volume 2794

    Abstract: Cholangiocarcinoma (CCA) is an aggressive malignancy of the bile ducts, with poor prognosis and limited treatment options. Here, we describe the integrated analysis of somatic mutations, RNA expression, copy number, and DNA methylation by The Cancer ... ...

    Abstract Cholangiocarcinoma (CCA) is an aggressive malignancy of the bile ducts, with poor prognosis and limited treatment options. Here, we describe the integrated analysis of somatic mutations, RNA expression, copy number, and DNA methylation by The Cancer Genome Atlas of a set of predominantly intrahepatic CCA cases and propose a molecular classification scheme. We identified an IDH mutant-enriched subtype with distinct molecular features including low expression of chromatin modifiers, elevated expression of mitochondrial genes, and increased mitochondrial DNA copy number. Leveraging the multi-platform data, we observed that ARID1A exhibited DNA hypermethylation and decreased expression in the IDH mutant subtype. More broadly, we found that IDH mutations are associated with an expanded histological spectrum of liver tumors with molecular features that stratify with CCA. Our studies reveal insights into the molecular pathogenesis and heterogeneity of cholangiocarcinoma and provide classification information of potential therapeutic significance.
    Keywords TCGA ; cholangiocarcinoma ; multi-omics ; integrative genomics ; DNA methylation ; RNA sequencing ; lncRNAs ; IDH ; whole exome ; ARID1A ; Biology (General) ; QH301-705.5
    Subject code 612
    Language English
    Publishing date 2017-03-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article ; Online: Integrative Genomic Analysis of Cholangiocarcinoma Identifies Distinct IDH-Mutant Molecular Profiles

    Farshad Farshidfar / Siyuan Zheng / Marie-Claude Gingras / Yulia Newton / Juliann Shih / A. Gordon Robertson / Toshinori Hinoue / Katherine A. Hoadley / Ewan A. Gibb / Jason Roszik / Kyle R. Covington / Chia-Chin Wu / Eve Shinbrot / Nicolas Stransky / Apurva Hegde / Ju Dong Yang / Ed Reznik / Sara Sadeghi / Chandra Sekhar Pedamallu /
    Akinyemi I. Ojesina / Julian M. Hess / J. Todd Auman / Suhn K. Rhie / Reanne Bowlby / Mitesh J. Borad / Rehan Akbani / Loretta K. Allotey / Adrian Ally / Domenico Alvaro / Jesper B. Andersen / Elizabeth L. Appelbaum / Arshi Arora / Miruna Balasundaram / Saianand Balu / Nabeel Bardeesy / Oliver F. Bathe / Stephen B. Baylin / Rameen Beroukhim / Mario Berrios / Tom Bodenheimer / Lori Boice / Moiz S. Bootwalla / Jay Bowen / Maria Consiglia Bragazzi / Denise Brooks / Vincenzo Cardinale / Rebecca Carlsen

    Cell Reports, Vol 19, Iss 13, Pp 2878-

    2017  Volume 2880

    Keywords Biology (General) ; QH301-705.5
    Language English
    Publishing date 2017-06-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article ; Online: Ampullary Cancers Harbor ELF3 Tumor Suppressor Gene Mutations and Exhibit Frequent WNT Dysregulation

    Marie-Claude Gingras / Kyle R. Covington / David K. Chang / Lawrence A. Donehower / Anthony J. Gill / Michael M. Ittmann / Chad J. Creighton / Amber L. Johns / Eve Shinbrot / Ninad Dewal / William E. Fisher / Christian Pilarsky / Robert Grützmann / Michael J. Overman / Nigel B. Jamieson / George Van Buren II / Jennifer Drummond / Kimberly Walker / Oliver A. Hampton /
    Liu Xi / Donna M. Muzny / Harsha Doddapaneni / Sandra L. Lee / Michelle Bellair / Jianhong Hu / Yi Han / Huyen H. Dinh / Mike Dahdouli / Jaswinder S. Samra / Peter Bailey / Nicola Waddell / John V. Pearson / Ivon Harliwong / Huamin Wang / Daniela Aust / Karin A. Oien / Ralph H. Hruban / Sally E. Hodges / Amy McElhany / Charupong Saengboonmee / Fraser R. Duthie / Sean M. Grimmond / Andrew V. Biankin / David A. Wheeler / Richard A. Gibbs

    Cell Reports, Vol 14, Iss 4, Pp 907-

    2016  Volume 919

    Abstract: The ampulla of Vater is a complex cellular environment from which adenocarcinomas arise to form a group of histopathologically heterogenous tumors. To evaluate the molecular features of these tumors, 98 ampullary adenocarcinomas were evaluated and ... ...

    Abstract The ampulla of Vater is a complex cellular environment from which adenocarcinomas arise to form a group of histopathologically heterogenous tumors. To evaluate the molecular features of these tumors, 98 ampullary adenocarcinomas were evaluated and compared to 44 distal bile duct and 18 duodenal adenocarcinomas. Genomic analyses revealed mutations in the WNT signaling pathway among half of the patients and in all three adenocarcinomas irrespective of their origin and histological morphology. These tumors were characterized by a high frequency of inactivating mutations of ELF3, a high rate of microsatellite instability, and common focal deletions and amplifications, suggesting common attributes in the molecular pathogenesis are at play in these tumors. The high frequency of WNT pathway activating mutation, coupled with small-molecule inhibitors of β-catenin in clinical trials, suggests future treatment decisions for these patients may be guided by genomic analysis.
    Keywords Biology (General) ; QH301-705.5
    Subject code 570
    Language English
    Publishing date 2016-02-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article ; Online: Multilevel Genomics-Based Taxonomy of Renal Cell Carcinoma

    Fengju Chen / Yiqun Zhang / Yasin Şenbabaoğlu / Giovanni Ciriello / Lixing Yang / Ed Reznik / Brian Shuch / Goran Micevic / Guillermo De Velasco / Eve Shinbrot / Michael S. Noble / Yiling Lu / Kyle R. Covington / Liu Xi / Jennifer A. Drummond / Donna Muzny / Hyojin Kang / Junehawk Lee / Pheroze Tamboli /
    Victor Reuter / Carl Simon Shelley / Benny A. Kaipparettu / Donald P. Bottaro / Andrew K. Godwin / Richard A. Gibbs / Gad Getz / Raju Kucherlapati / Peter J. Park / Chris Sander / Elizabeth P. Henske / Jane H. Zhou / David J. Kwiatkowski / Thai H. Ho / Toni K. Choueiri / James J. Hsieh / Rehan Akbani / Gordon B. Mills / A. Ari Hakimi / David A. Wheeler / Chad J. Creighton

    Cell Reports, Vol 14, Iss 10, Pp 2476-

    2016  Volume 2489

    Abstract: On the basis of multidimensional and comprehensive molecular characterization (including DNA methalylation and copy number, RNA, and protein expression), we classified 894 renal cell carcinomas (RCCs) of various histologic types into nine major genomic ... ...

    Abstract On the basis of multidimensional and comprehensive molecular characterization (including DNA methalylation and copy number, RNA, and protein expression), we classified 894 renal cell carcinomas (RCCs) of various histologic types into nine major genomic subtypes. Site of origin within the nephron was one major determinant in the classification, reflecting differences among clear cell, chromophobe, and papillary RCC. Widespread molecular changes associated with TFE3 gene fusion or chromatin modifier genes were present within a specific subtype and spanned multiple subtypes. Differences in patient survival and in alteration of specific pathways (including hypoxia, metabolism, MAP kinase, NRF2-ARE, Hippo, immune checkpoint, and PI3K/AKT/mTOR) could further distinguish the subtypes. Immune checkpoint markers and molecular signatures of T cell infiltrates were both highest in the subtype associated with aggressive clear cell RCC. Differences between the genomic subtypes suggest that therapeutic strategies could be tailored to each RCC disease subset.
    Keywords Biology (General) ; QH301-705.5
    Subject code 616
    Language English
    Publishing date 2016-03-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article ; Online: Integrated Genomic Analysis of the Ubiquitin Pathway across Cancer Types

    Zhongqi Ge / Jake S. Leighton / Yumeng Wang / Xinxin Peng / Zhongyuan Chen / Hu Chen / Yutong Sun / Fan Yao / Jun Li / Huiwen Zhang / Jianfang Liu / Craig D. Shriver / Hai Hu / Helen Piwnica-Worms / Li Ma / Han Liang / Samantha J. Caesar-Johnson / John A. Demchok / Ina Felau /
    Melpomeni Kasapi / Martin L. Ferguson / Carolyn M. Hutter / Heidi J. Sofia / Roy Tarnuzzer / Zhining Wang / Liming Yang / Jean C. Zenklusen / Jiashan (Julia) Zhang / Sudha Chudamani / Jia Liu / Laxmi Lolla / Rashi Naresh / Todd Pihl / Qiang Sun / Yunhu Wan / Ye Wu / Juok Cho / Timothy DeFreitas / Scott Frazer / Nils Gehlenborg / Gad Getz / David I. Heiman / Jaegil Kim / Michael S. Lawrence / Pei Lin / Sam Meier / Michael S. Noble / Gordon Saksena / Doug Voet / Hailei Zhang / Brady Bernard / Nyasha Chambwe / Varsha Dhankani / Theo Knijnenburg / Roger Kramer / Kalle Leinonen / Yuexin Liu / Michael Miller / Sheila Reynolds / Ilya Shmulevich / Vesteinn Thorsson / Wei Zhang / Rehan Akbani / Bradley M. Broom / Apurva M. Hegde / Zhenlin Ju / Rupa S. Kanchi / Anil Korkut / Shiyun Ling / Wenbin Liu / Yiling Lu / Gordon B. Mills / Kwok-Shing Ng / Arvind Rao / Michael Ryan / Jing Wang / John N. Weinstein / Jiexin Zhang / Adam Abeshouse / Joshua Armenia / Debyani Chakravarty / Walid K. Chatila / Ino de Bruijn / Jianjiong Gao / Benjamin E. Gross / Zachary J. Heins / Ritika Kundra / Konnor La / Marc Ladanyi / Augustin Luna / Moriah G. Nissan / Angelica Ochoa / Sarah M. Phillips / Ed Reznik / Francisco Sanchez-Vega / Chris Sander / Nikolaus Schultz / Robert Sheridan / S. Onur Sumer / Yichao Sun / Barry S. Taylor / Jioajiao Wang / Hongxin Zhang / Pavana Anur / Myron Peto / Paul Spellman / Christopher Benz / Joshua M. Stuart / Christopher K. Wong / Christina Yau / D. Neil Hayes / Joel S. Parker / Matthew D. Wilkerson / Adrian Ally / Miruna Balasundaram / Reanne Bowlby / Denise Brooks / Rebecca Carlsen / Eric Chuah / Noreen Dhalla / Robert Holt / Steven J.M. Jones / Katayoon Kasaian / Darlene Lee / Yussanne Ma / Marco A. Marra / Michael Mayo / Richard A. Moore / Andrew J. Mungall / Karen Mungall / A. Gordon Robertson / Sara Sadeghi / Jacqueline E. Schein / Payal Sipahimalani / Angela Tam / Nina Thiessen / Kane Tse / Tina Wong / Ashton C. Berger / Rameen Beroukhim / Andrew D. Cherniack / Carrie Cibulskis / Stacey B. Gabriel / Galen F. Gao / Gavin Ha / Matthew Meyerson / Steven E. Schumacher / Juliann Shih / Melanie H. Kucherlapati / Raju S. Kucherlapati / Stephen Baylin / Leslie Cope / Ludmila Danilova / Moiz S. Bootwalla / Phillip H. Lai / Dennis T. Maglinte / David J. Van Den Berg / Daniel J. Weisenberger / J. Todd Auman / Saianand Balu / Tom Bodenheimer / Cheng Fan / Katherine A. Hoadley / Alan P. Hoyle / Stuart R. Jefferys / Corbin D. Jones / Shaowu Meng / Piotr A. Mieczkowski / Lisle E. Mose / Amy H. Perou / Charles M. Perou / Jeffrey Roach / Yan Shi / Janae V. Simons / Tara Skelly / Matthew G. Soloway / Donghui Tan / Umadevi Veluvolu / Huihui Fan / Toshinori Hinoue / Peter W. Laird / Hui Shen / Wanding Zhou / Michelle Bellair / Kyle Chang / Kyle Covington / Chad J. Creighton / Huyen Dinh / HarshaVardhan Doddapaneni / Lawrence A. Donehower / Jennifer Drummond / Richard A. Gibbs / Robert Glenn / Walker Hale / Yi Han / Jianhong Hu / Viktoriya Korchina / Sandra Lee / Lora Lewis / Wei Li / Xiuping Liu / Margaret Morgan / Donna Morton / Donna Muzny / Jireh Santibanez / Margi Sheth / Eve Shinbrot / Linghua Wang / Min Wang / David A. Wheeler / Liu Xi / Fengmei Zhao / Julian Hess / Elizabeth L. Appelbaum / Matthew Bailey / Matthew G. Cordes / Li Ding / Catrina C. Fronick / Lucinda A. Fulton / Robert S. Fulton / Cyriac Kandoth / Elaine R. Mardis / Michael D. McLellan / Christopher A. Miller / Heather K. Schmidt / Richard K. Wilson / Daniel Crain / Erin Curley / Johanna Gardner / Kevin Lau / David Mallery / Scott Morris / Joseph Paulauskis / Robert Penny / Candace Shelton / Troy Shelton / Mark Sherman / Eric Thompson / Peggy Yena / Jay Bowen / Julie M. Gastier-Foster / Mark Gerken / Kristen M. Leraas / Tara M. Lichtenberg / Nilsa C. Ramirez / Lisa Wise / Erik Zmuda / Niall Corcoran / Tony Costello / Christopher Hovens / Andre L. Carvalho / Ana C. de Carvalho / José H. Fregnani / Adhemar Longatto-Filho / Rui M. Reis / Cristovam Scapulatempo-Neto / Henrique C.S. Silveira / Daniel O. Vidal / Andrew Burnette / Jennifer Eschbacher / Beth Hermes / Ardene Noss / Rosy Singh / Matthew L. Anderson / Patricia D. Castro / Michael Ittmann / David Huntsman / Bernard Kohl / Xuan Le / Richard Thorp / Chris Andry / Elizabeth R. Duffy / Vladimir Lyadov / Oxana Paklina / Galiya Setdikova / Alexey Shabunin / Mikhail Tavobilov / Christopher McPherson / Ronald Warnick / Ross Berkowitz / Daniel Cramer / Colleen Feltmate / Neil Horowitz / Adam Kibel / Michael Muto / Chandrajit P. Raut / Andrei Malykh / Jill S. Barnholtz-Sloan / Wendi Barrett / Karen Devine / Jordonna Fulop / Quinn T. Ostrom / Kristen Shimmel / Yingli Wolinsky / Andrew E. Sloan / Agostino De Rose / Felice Giuliante / Marc Goodman / Beth Y. Karlan / Curt H. Hagedorn / John Eckman / Jodi Harr / Jerome Myers / Kelinda Tucker / Leigh Anne Zach / Brenda Deyarmin / Leonid Kvecher / Caroline Larson / Richard J. Mural / Stella Somiari / Ales Vicha / Tomas Zelinka / Joseph Bennett / Mary Iacocca / Brenda Rabeno / Patricia Swanson / Mathieu Latour / Louis Lacombe / Bernard Têtu / Alain Bergeron / Mary McGraw / Susan M. Staugaitis / John Chabot / Hanina Hibshoosh / Antonia Sepulveda / Tao Su / Timothy Wang / Olga Potapova / Olga Voronina / Laurence Desjardins / Odette Mariani / Sergio Roman-Roman / Xavier Sastre / Marc-Henri Stern / Feixiong Cheng / Sabina Signoretti / Andrew Berchuck / Darell Bigner / Eric Lipp / Jeffrey Marks / Shannon McCall / Roger McLendon / Angeles Secord / Alexis Sharp / Madhusmita Behera / Daniel J. Brat / Amy Chen / Keith Delman / Seth Force / Fadlo Khuri / Kelly Magliocca / Shishir Maithel / Jeffrey J. Olson / Taofeek Owonikoko / Alan Pickens / Suresh Ramalingam / Dong M. Shin / Gabriel Sica / Erwin G. Van Meir / Hongzheng Zhang / Wil Eijckenboom / Ad Gillis / Esther Korpershoek / Leendert Looijenga / Wolter Oosterhuis / Hans Stoop / Kim E. van Kessel / Ellen C. Zwarthoff / Chiara Calatozzolo / Lucia Cuppini / Stefania Cuzzubbo / Francesco DiMeco / Gaetano Finocchiaro / Luca Mattei / Alessandro Perin / Bianca Pollo / Chu Chen / John Houck / Pawadee Lohavanichbutr / Arndt Hartmann / Christine Stoehr / Robert Stoehr / Helge Taubert / Sven Wach / Bernd Wullich / Witold Kycler / Dawid Murawa / Maciej Wiznerowicz / Ki Chung / W. Jeffrey Edenfield / Julie Martin / Eric Baudin / Glenn Bubley / Raphael Bueno / Assunta De Rienzo / William G. Richards / Steven Kalkanis / Tom Mikkelsen / Houtan Noushmehr / Lisa Scarpace / Nicolas Girard / Marta Aymerich / Elias Campo / Eva Giné / Armando López Guillermo / Nguyen Van Bang / Phan Thi Hanh / Bui Duc Phu / Yufang Tang / Howard Colman / Kimberley Evason / Peter R. Dottino / John A. 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Kovatich / John DiPersio / Bettina Drake / Ramaswamy Govindan / Sharon Heath / Timothy Ley / Brian Van Tine / Peter Westervelt / Mark A. Rubin / Jung Il Lee / Natália D. Aredes / Armaz Mariamidze

    Cell Reports, Vol 23, Iss 1, Pp 213-226.e

    2018  Volume 3

    Abstract: Summary: Protein ubiquitination is a dynamic and reversible process of adding single ubiquitin molecules or various ubiquitin chains to target proteins. Here, using multidimensional omic data of 9,125 tumor samples across 33 cancer types from The Cancer ... ...

    Abstract Summary: Protein ubiquitination is a dynamic and reversible process of adding single ubiquitin molecules or various ubiquitin chains to target proteins. Here, using multidimensional omic data of 9,125 tumor samples across 33 cancer types from The Cancer Genome Atlas, we perform comprehensive molecular characterization of 929 ubiquitin-related genes and 95 deubiquitinase genes. Among them, we systematically identify top somatic driver candidates, including mutated FBXW7 with cancer-type-specific patterns and amplified MDM2 showing a mutually exclusive pattern with BRAF mutations. Ubiquitin pathway genes tend to be upregulated in cancer mediated by diverse mechanisms. By integrating pan-cancer multiomic data, we identify a group of tumor samples that exhibit worse prognosis. These samples are consistently associated with the upregulation of cell-cycle and DNA repair pathways, characterized by mutated TP53, MYC/TERT amplification, and APC/PTEN deletion. Our analysis highlights the importance of the ubiquitin pathway in cancer development and lays a foundation for developing relevant therapeutic strategies. : Ge et al. analyze a cohort of 9,125 TCGA samples across 33 cancer types to provide a comprehensive characterization of the ubiquitin pathway. They detect somatic driver candidates in the ubiquitin pathway and identify a cluster of patients with poor survival, highlighting the importance of this pathway in cancer development. Keywords: ubiquitin pathway, pan-cancer analysis, The Cancer Genome Atlas, tumor subtype, cancer prognosis, therapeutic targets, biomarker, FBXW7
    Keywords Biology (General) ; QH301-705.5
    Language English
    Publishing date 2018-04-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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