Literature DB >> 26841357

mutation3D: Cancer Gene Prediction Through Atomic Clustering of Coding Variants in the Structural Proteome.

Michael J Meyer1,2,3, Ryan Lapcevic1,2, Alfonso E Romero4, Mark Yoon1,2, Jishnu Das1,2, Juan Felipe Beltrán1,2, Matthew Mort5, Peter D Stenson5, David N Cooper5, Alberto Paccanaro4, Haiyuan Yu1,2.   

Abstract

A new algorithm and Web server, mutation3D (http://mutation3d.org), proposes driver genes in cancer by identifying clusters of amino acid substitutions within tertiary protein structures. We demonstrate the feasibility of using a 3D clustering approach to implicate proteins in cancer based on explorations of single proteins using the mutation3D Web interface. On a large scale, we show that clustering with mutation3D is able to separate functional from nonfunctional mutations by analyzing a combination of 8,869 known inherited disease mutations and 2,004 SNPs overlaid together upon the same sets of crystal structures and homology models. Further, we present a systematic analysis of whole-genome and whole-exome cancer datasets to demonstrate that mutation3D identifies many known cancer genes as well as previously underexplored target genes. The mutation3D Web interface allows users to analyze their own mutation data in a variety of popular formats and provides seamless access to explore mutation clusters derived from over 975,000 somatic mutations reported by 6,811 cancer sequencing studies. The mutation3D Web interface is freely available with all major browsers supported.
© 2016 WILEY PERIODICALS, INC.

Entities:  

Keywords:  Web tool; cancer; clustering; protein structures; somatic mutations

Mesh:

Substances:

Year:  2016        PMID: 26841357      PMCID: PMC4833594          DOI: 10.1002/humu.22963

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  38 in total

1.  OncodriveCLUST: exploiting the positional clustering of somatic mutations to identify cancer genes.

Authors:  David Tamborero; Abel Gonzalez-Perez; Nuria Lopez-Bigas
Journal:  Bioinformatics       Date:  2013-07-24       Impact factor: 6.937

Review 2.  Exploring mechanisms of human disease through structurally resolved protein interactome networks.

Authors:  Robert Fragoza; Hao Ran Lee; Nicolas A Cordero; Jishnu Das; Yu Guo; Michael J Meyer; Tommy V Vo; Xiujuan Wang; Haiyuan Yu
Journal:  Mol Biosyst       Date:  2014-01

3.  Elucidating common structural features of human pathogenic variations using large-scale atomic-resolution protein networks.

Authors:  Jishnu Das; Hao Ran Lee; Adithya Sagar; Robert Fragoza; Jin Liang; Xiaomu Wei; Xiujuan Wang; Matthew Mort; Peter D Stenson; David N Cooper; Haiyuan Yu
Journal:  Hum Mutat       Date:  2014-04-07       Impact factor: 4.878

4.  Cancer missense mutations alter binding properties of proteins and their interaction networks.

Authors:  Hafumi Nishi; Manoj Tyagi; Shaolei Teng; Benjamin A Shoemaker; Kosuke Hashimoto; Emil Alexov; Stefan Wuchty; Anna R Panchenko
Journal:  PLoS One       Date:  2013-06-14       Impact factor: 3.240

5.  High resolution melting analysis of KRAS, BRAF and PIK3CA in KRAS exon 2 wild-type metastatic colorectal cancer.

Authors:  Joana G Guedes; Isabel Veiga; Patrícia Rocha; Pedro Pinto; Carla Pinto; Manuela Pinheiro; Ana Peixoto; Maria Fragoso; Ana Raimundo; Paula Ferreira; Manuela Machado; Nuno Sousa; Paula Lopes; António Araújo; Joana Macedo; Fernando Alves; Camila Coutinho; Rui Henrique; Lúcio L Santos; Manuel R Teixeira
Journal:  BMC Cancer       Date:  2013-04-01       Impact factor: 4.430

6.  Detecting patches of protein sites of influenza A viruses under positive selection.

Authors:  Christina Tusche; Lars Steinbrück; Alice C McHardy
Journal:  Mol Biol Evol       Date:  2012-03-16       Impact factor: 16.240

Review 7.  The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine.

Authors:  Peter D Stenson; Matthew Mort; Edward V Ball; Katy Shaw; Andrew Phillips; David N Cooper
Journal:  Hum Genet       Date:  2014-01       Impact factor: 4.132

8.  Discovery and saturation analysis of cancer genes across 21 tumour types.

Authors:  Michael S Lawrence; Petar Stojanov; Craig H Mermel; James T Robinson; Levi A Garraway; Todd R Golub; Matthew Meyerson; Stacey B Gabriel; Eric S Lander; Gad Getz
Journal:  Nature       Date:  2014-01-05       Impact factor: 49.962

9.  Signatures of mutational processes in human cancer.

Authors:  Ludmil B Alexandrov; Serena Nik-Zainal; David C Wedge; Samuel A J R Aparicio; Sam Behjati; Andrew V Biankin; Graham R Bignell; Niccolò Bolli; Ake Borg; Anne-Lise Børresen-Dale; Sandrine Boyault; Birgit Burkhardt; Adam P Butler; Carlos Caldas; Helen R Davies; Christine Desmedt; Roland Eils; Jórunn Erla Eyfjörd; John A Foekens; Mel Greaves; Fumie Hosoda; Barbara Hutter; Tomislav Ilicic; Sandrine Imbeaud; Marcin Imielinski; Marcin Imielinsk; Natalie Jäger; David T W Jones; David Jones; Stian Knappskog; Marcel Kool; Sunil R Lakhani; Carlos López-Otín; Sancha Martin; Nikhil C Munshi; Hiromi Nakamura; Paul A Northcott; Marina Pajic; Elli Papaemmanuil; Angelo Paradiso; John V Pearson; Xose S Puente; Keiran Raine; Manasa Ramakrishna; Andrea L Richardson; Julia Richter; Philip Rosenstiel; Matthias Schlesner; Ton N Schumacher; Paul N Span; Jon W Teague; Yasushi Totoki; Andrew N J Tutt; Rafael Valdés-Mas; Marit M van Buuren; Laura van 't Veer; Anne Vincent-Salomon; Nicola Waddell; Lucy R Yates; Jessica Zucman-Rossi; P Andrew Futreal; Ultan McDermott; Peter Lichter; Matthew Meyerson; Sean M Grimmond; Reiner Siebert; Elías Campo; Tatsuhiro Shibata; Stefan M Pfister; Peter J Campbell; Michael R Stratton
Journal:  Nature       Date:  2013-08-14       Impact factor: 49.962

10.  Mutational heterogeneity in cancer and the search for new cancer-associated genes.

Authors:  Michael S Lawrence; Petar Stojanov; Paz Polak; Gregory V Kryukov; Kristian Cibulskis; Andrey Sivachenko; Scott L Carter; Chip Stewart; Craig H Mermel; Steven A Roberts; Adam Kiezun; Peter S Hammerman; Aaron McKenna; Yotam Drier; Lihua Zou; Alex H Ramos; Trevor J Pugh; Nicolas Stransky; Elena Helman; Jaegil Kim; Carrie Sougnez; Lauren Ambrogio; Elizabeth Nickerson; Erica Shefler; Maria L Cortés; Daniel Auclair; Gordon Saksena; Douglas Voet; Michael Noble; Daniel DiCara; Pei Lin; Lee Lichtenstein; David I Heiman; Timothy Fennell; Marcin Imielinski; Bryan Hernandez; Eran Hodis; Sylvan Baca; Austin M Dulak; Jens Lohr; Dan-Avi Landau; Catherine J Wu; Jorge Melendez-Zajgla; Alfredo Hidalgo-Miranda; Amnon Koren; Steven A McCarroll; Jaume Mora; Brian Crompton; Robert Onofrio; Melissa Parkin; Wendy Winckler; Kristin Ardlie; Stacey B Gabriel; Charles W M Roberts; Jaclyn A Biegel; Kimberly Stegmaier; Adam J Bass; Levi A Garraway; Matthew Meyerson; Todd R Golub; Dmitry A Gordenin; Shamil Sunyaev; Eric S Lander; Gad Getz
Journal:  Nature       Date:  2013-06-16       Impact factor: 49.962

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  31 in total

1.  Comparison of algorithms for the detection of cancer drivers at subgene resolution.

Authors:  Eduard Porta-Pardo; Atanas Kamburov; David Tamborero; Tirso Pons; Daniela Grases; Alfonso Valencia; Nuria Lopez-Bigas; Gad Getz; Adam Godzik
Journal:  Nat Methods       Date:  2017-07-17       Impact factor: 28.547

2.  Recurrent somatic mutations affecting B-cell receptor signaling pathway genes in follicular lymphoma.

Authors:  Kilannin Krysiak; Felicia Gomez; Brian S White; Matthew Matlock; Christopher A Miller; Lee Trani; Catrina C Fronick; Robert S Fulton; Friederike Kreisel; Amanda F Cashen; Kenneth R Carson; Melissa M Berrien-Elliott; Nancy L Bartlett; Malachi Griffith; Obi L Griffith; Todd A Fehniger
Journal:  Blood       Date:  2016-11-14       Impact factor: 22.113

3.  Okur-Chung neurodevelopmental syndrome-linked CK2α variants have reduced kinase activity.

Authors:  I Dominguez; J M Cruz-Gamero; V Corasolla; N Dacher; S Rangasamy; A Urbani; V Narayanan; H Rebholz
Journal:  Hum Genet       Date:  2021-05-04       Impact factor: 4.132

Review 4.  Functional variomics and network perturbation: connecting genotype to phenotype in cancer.

Authors:  Song Yi; Shengda Lin; Yongsheng Li; Wei Zhao; Gordon B Mills; Nidhi Sahni
Journal:  Nat Rev Genet       Date:  2017-03-27       Impact factor: 53.242

5.  De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation.

Authors:  Dongxue Mao; Chloe M Reuter; Maura R Z Ruzhnikov; Anita E Beck; Emily G Farrow; Lisa T Emrick; Jill A Rosenfeld; Katherine M Mackenzie; Laurie Robak; Matthew T Wheeler; Lindsay C Burrage; Mahim Jain; Pengfei Liu; Daniel Calame; Sébastien Küry; Martin Sillesen; Klaus Schmitz-Abe; Davide Tonduti; Luigina Spaccini; Maria Iascone; Casie A Genetti; Mary K Koenig; Madeline Graf; Alyssa Tran; Mercedes Alejandro; Brendan H Lee; Isabelle Thiffault; Pankaj B Agrawal; Jonathan A Bernstein; Hugo J Bellen; Hsiao-Tuan Chao
Journal:  Am J Hum Genet       Date:  2020-03-19       Impact factor: 11.025

6.  Comprehensive Analysis of Constraint on the Spatial Distribution of Missense Variants in Human Protein Structures.

Authors:  R Michael Sivley; Xiaoyi Dou; Jens Meiler; William S Bush; John A Capra
Journal:  Am J Hum Genet       Date:  2018-02-15       Impact factor: 11.025

7.  Exploiting ion channel structure to assess rare variant pathogenicity.

Authors:  Brett M Kroncke; Tao Yang; Prince Kannankeril; M Benjamin Shoemaker; Dan M Roden
Journal:  Heart Rhythm       Date:  2018-01-09       Impact factor: 6.343

8.  Bayesian inference of negative and positive selection in human cancers.

Authors:  Donate Weghorn; Shamil Sunyaev
Journal:  Nat Genet       Date:  2017-11-06       Impact factor: 38.330

9.  In-depth and 3-dimensional exploration of the budding yeast phosphoproteome.

Authors:  Michael C Lanz; Kumar Yugandhar; Shagun Gupta; Ethan J Sanford; Vitor M Faça; Stephanie Vega; Aaron M N Joiner; J Christopher Fromme; Haiyuan Yu; Marcus B Smolka
Journal:  EMBO Rep       Date:  2021-01-25       Impact factor: 8.807

10.  Structure analysis of deleterious nsSNPs in human PALB2 protein for functional inference.

Authors:  Noshin Nawar; Anik Paul; Hamida Nooreen Mahmood; Md Ismail Faisal; Md Ismail Hosen; Hossain Uddin Shekhar
Journal:  Bioinformation       Date:  2021-03-31
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