Literature DB >> 18645599

The application of single nucleotide polymorphism microarrays in cancer research.

Xueying Mao1, Bryan D Young, Yong-Jie Lu.   

Abstract

The development of microarray technology has had a significant impact on the genetic analysis of human disease. The recently developed single nucleotide polymorphism (SNP) array can be used to measure both DNA polymorphism and dosage changes. Our laboratory has applied SNP microarray analysis to uncover frequent uniparental disomies and sub-microscopic genomic copy number gains and losses in different cancers. This review will focus on the wide range of applications of SNP microarray analysis to cancer research. SNP array genotyping can determine loss of heterozygosity, genomic copy number changes and DNA methylation alterations of cancer cells. The same technology can also be used to investigate allelic association in cancers. Therefore, it can be applied to the identification of cancer predisposition genes, oncogenes and tumor suppressor genes in specific types of tumors. As a consequence, they have potential in cancer risk assessment, diagnosis, prognosis and treatment selection.

Entities:  

Keywords:  SNP array; cancer; copy number change; genome-wide analysis; genotyping

Year:  2007        PMID: 18645599      PMCID: PMC2430687          DOI: 10.2174/138920207781386924

Source DB:  PubMed          Journal:  Curr Genomics        ISSN: 1389-2029            Impact factor:   2.236


  77 in total

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Authors:  J Guillermo Paez; Ming Lin; Rameen Beroukhim; Jeffrey C Lee; Xiaojun Zhao; Daniel J Richter; Stacey Gabriel; Paula Herman; Hidefumi Sasaki; David Altshuler; Cheng Li; Matthew Meyerson; William R Sellers
Journal:  Nucleic Acids Res       Date:  2004-05-18       Impact factor: 16.971

2.  Allelic imbalance analysis by high-density single-nucleotide polymorphic allele (SNP) array with whole genome amplified DNA.

Authors:  Kwong-Kwok Wong; Yvonne T M Tsang; Jianhe Shen; Rita S Cheng; Yi-Mieng Chang; Tsz-Kwong Man; Ching C Lau
Journal:  Nucleic Acids Res       Date:  2004-05-17       Impact factor: 16.971

3.  Highly parallel SNP genotyping.

Authors:  J B Fan; A Oliphant; R Shen; B G Kermani; F Garcia; K L Gunderson; M Hansen; F Steemers; S L Butler; P Deloukas; L Galver; S Hunt; C McBride; M Bibikova; T Rubano; J Chen; E Wickham; D Doucet; W Chang; D Campbell; B Zhang; S Kruglyak; D Bentley; J Haas; P Rigault; L Zhou; J Stuelpnagel; M S Chee
Journal:  Cold Spring Harb Symp Quant Biol       Date:  2003

4.  Reliable high-throughput genotyping and loss-of-heterozygosity detection in formalin-fixed, paraffin-embedded tumors using single nucleotide polymorphism arrays.

Authors:  Esther H Lips; Jan Willem F Dierssen; Ronald van Eijk; Jan Oosting; Paul H C Eilers; Rob A E M Tollenaar; Eelco J de Graaf; Ruben van't Slot; Cisca Wijmenga; Hans Morreau; Tom van Wezel
Journal:  Cancer Res       Date:  2005-11-15       Impact factor: 12.701

5.  Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays.

Authors:  K Lindblad-Toh; D M Tanenbaum; M J Daly; E Winchester; W O Lui; A Villapakkam; S E Stanton; C Larsson; T J Hudson; B E Johnson; E S Lander; M Meyerson
Journal:  Nat Biotechnol       Date:  2000-09       Impact factor: 54.908

6.  Novel pheochromocytoma susceptibility loci identified by integrative genomics.

Authors:  Patricia L M Dahia; Ke Hao; John Rogus; Christian Colin; Miguel A G Pujana; Ken Ross; Danielle Magoffin; Neil Aronin; Alberto Cascon; César Y Hayashida; Cheng Li; Sérgio P A Toledo; Charles D Stiles
Journal:  Cancer Res       Date:  2005-11-01       Impact factor: 12.701

7.  High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays.

Authors:  D Pinkel; R Segraves; D Sudar; S Clark; I Poole; D Kowbel; C Collins; W L Kuo; C Chen; Y Zhai; S H Dairkee; B M Ljung; J W Gray; D G Albertson
Journal:  Nat Genet       Date:  1998-10       Impact factor: 38.330

8.  High-resolution single-nucleotide polymorphism array and clustering analysis of loss of heterozygosity in human lung cancer cell lines.

Authors:  Pasi A Jänne; Cheng Li; Xiaojun Zhao; Luc Girard; Tzu-Hsiu Chen; John Minna; David C Christiani; Bruce E Johnson; Matthew Meyerson
Journal:  Oncogene       Date:  2004-04-08       Impact factor: 9.867

9.  Rapid high-resolution karyotyping with precise identification of chromosome breakpoints.

Authors:  Xueying Mao; Sharon Y James; Rafael J Yáñez-Muñoz; Tracy Chaplin; Gael Molloy; R Tim D Oliver; Bryan D Young; Yong-Jie Lu
Journal:  Genes Chromosomes Cancer       Date:  2007-07       Impact factor: 5.006

10.  Assessment of submicroscopic genetic lesions by single nucleotide polymorphism arrays in a child with acute myeloid leukemia and FLT3-internal tandem duplication.

Authors:  Silvia Bungaro; Manoj Raghavan; Maria Grazia Dell'Oro; Paolo Paolucci; Bryan D Young; Andrea Biondi; Giovanni Cazzaniga
Journal:  Haematologica       Date:  2006-06-01       Impact factor: 9.941

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  9 in total

1.  Array-based karyotyping for prognostic assessment in chronic lymphocytic leukemia: performance comparison of Affymetrix 10K2.0, 250K Nsp, and SNP6.0 arrays.

Authors:  Jill M Hagenkord; Federico A Monzon; Shera F Kash; Stan Lilleberg; Qingmei Xie; Jeffrey A Kant
Journal:  J Mol Diagn       Date:  2010-01-14       Impact factor: 5.568

2.  Genome-wide association study on susceptibility genes associated with yang-deficiency constitution: A small sample case-control study.

Authors:  Shi-lin Yao; Qi Wang; Zu-zhi Zhang; Jun-xia Wu; Nan Cheng; Xia Xu; Guang-yan Xie; Jian Cao
Journal:  Chin J Integr Med       Date:  2014-12-22       Impact factor: 1.978

3.  Proteomics, pathway array and signaling network-based medicine in cancer.

Authors:  David Y Zhang; Fei Ye; Ling Gao; Xiaoliang Liu; Xin Zhao; Yufang Che; Hongxia Wang; Libo Wang; Josephine Wu; Dong Song; Wei Liu; Hong Xu; Bo Jiang; Weijia Zhang; Jinhua Wang; Peng Lee
Journal:  Cell Div       Date:  2009-10-28       Impact factor: 5.130

Review 4.  The complexity of prostate cancer: genomic alterations and heterogeneity.

Authors:  Lara K Boyd; Xueying Mao; Yong-Jie Lu
Journal:  Nat Rev Urol       Date:  2012-11       Impact factor: 14.432

5.  An Efficient Genotyping Method in Chicken Based on Genome Reducing and Sequencing.

Authors:  Rongrong Liao; Zhen Wang; Qiang Chen; Yingying Tu; Zhenliang Chen; Qishan Wang; Changsuo Yang; Xiangzhe Zhang; Yuchun Pan
Journal:  PLoS One       Date:  2015-08-27       Impact factor: 3.240

6.  Genetic variations analysis for complex brain disease diagnosis using machine learning techniques: opportunities and hurdles.

Authors:  Hala Ahmed; Louai Alarabi; Shaker El-Sappagh; Hassan Soliman; Mohammed Elmogy
Journal:  PeerJ Comput Sci       Date:  2021-09-20

7.  Toll-like receptors and human disease: lessons from single nucleotide polymorphisms.

Authors:  Yi-Tzu Lin; Amanda Verma; Conrad P Hodgkinson
Journal:  Curr Genomics       Date:  2012-12       Impact factor: 2.236

Review 8.  SNPs Array Karyotyping in Non-Hodgkin Lymphoma.

Authors:  Maryam Etebari; Mohsen Navari; Pier Paolo Piccaluga
Journal:  Microarrays (Basel)       Date:  2015-11-12

9.  Clonal relationship of synchronous head and neck cancer and esophageal cancer assessed by single nucleotide polymorphism-based loss of heterozygosity analysis.

Authors:  Somkiat Sunpaweravong; Sacarin Bunbanjerdsuk; Tanjitti Pongrujikorn; Chaiwat Naktang; Patrapim Sunpaweravong; Anupong Nitiruangjaras; Tanadech Dechaphankul; Natini Jinawath
Journal:  BMC Cancer       Date:  2019-12-03       Impact factor: 4.430

  9 in total

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