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Heritable clustering and pathway discovery in breast cancer integrating epigenetic and phenotypic data.

Heritable clustering and pathway discovery in breast cancer integrating epigenetic and phenotypic data. Research Abstract Details 

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  • Heritable clustering and pathway discovery in breast cancer integrating epigenetic and phenotypic data. Abstract Text:

    zailong wangZailong Wang,pearlly yanPearlly Yan,dustin potterDustin Potter,charis engCharis Eng,tim h-m huangTim H-M Huang,shili linShili Lin,

    BACKGROUND: In order to recapitulate tumor progression pathways using epigenetic data, we developed novel clustering and pathway reconstruction algorithms, collectively referred to as heritable clustering. This approach generates a progression model of altered DNA methylation from tumor tissues diagnosed at different developmental stages. The samples act as surrogates for natural progression in breast cancer and allow the algorithm to uncover distinct epigenotypes that describe the molecular events underlying this process. Furthermore, our likelihood-based clustering algorithm has great flexibility, allowing for incomplete epigenotype or clinical phenotype data and also permitting dependencies among variables. RESULTS: Using this heritable clustering approach, we analyzed methylation data obtained from 86 primary breast cancers to recapitulate pathways of breast tumor progression. Detailed annotation and interpretation are provided to the optimal pathway recapitulated. The result confirms the previous observation that aggressive tumors tend to exhibit higher levels of promoter hypermethylation. CONCLUSION: Our results indicate that the proposed heritable clustering algorithms are a useful tool for stratifying both methylation and clinical variables of breast cancer. The application to the breast tumor data illustrates that this approach can select meaningful progression models which may aid the interpretation of pathways having biological and clinical significance. Furthermore, the framework allows for other types of biological data, such as microarray gene expression or array CGH data, to be integrated.

    Heritable clustering and pathway discovery in breast cancer integrating epigenetic and phenotypic data. Publishing Authors By Initials

    z wangZ Wang,p yanP Yan,d potterD Potter,c engC Eng,th huangTH Huang,s linS Lin,

    For similar natural sciences: science: systems integration research abstracts see: natural sciences: science: systems integration research

    PUBMED ID PMID:

    MEDLINE DATE:

    Heritable clustering and pathway discovery in breast cancer integrating epigenetic and phenotypic data. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: BMC bioinformatics

    VOLUME: 8

    Page Numbers: 38

    Journal Abbreviation: BMC Bioinformatics

    ISSN: 1471-2105

    DAY: 1

    MONTH: 02

    YEAR: 2007

    Heritable clustering and pathway discovery in breast cancer integrating epigenetic and phenotypic data. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 100965194

    Heritable clustering and pathway discovery in breast cancer integrating epigenetic and phenotypic data. Keywords Mesh Terms:

    KEYWORDS: Systems Integration

    MESH TERMS: genetics

    Chemical & Substance for Abstract: Heritable clustering and pathway discovery in breast cancer integrating epigenetic and phenotypic data. Information

    Substance Name: Neoplasm Proteins

    Registry Number: 0

    Grant and Affiliation Information for Heritable clustering and pathway discovery in breast cancer integrating epigenetic and phenotypic data.

    AFFILIATION: Mathematical Biosciences Institute, The Ohio State University, 231 W, 18th Avenue, Columbus, OH 43210, USA. zailong.wang@yahoo.com <zailong.wang@yahoo.com>

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NCI

    GRANT: T32-CA106196-03

    ACRONYM: CA

    MEDLINETA: BMC Bioinformatics

    REFSOURCE:

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