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Forerunner genes contiguous to RB1 contribute to the development of in situ neoplasia.

Forerunner genes contiguous to RB1 contribute to the development of in situ neoplasia. Research Abstract Details 

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  • Forerunner genes contiguous to RB1 contribute to the development of in situ neoplasia. Abstract Text:

    sangkyou leeSangkyou Lee,joon jeongJoon Jeong,tadeusz majewskiTadeusz Majewski,steven e schererSteven E Scherer,mi-sook kimMi-Sook Kim,tomasz tuziakTomasz Tuziak,kuang s tangKuang S Tang,keith baggerlyKeith Baggerly,herbert barton grossmanHerbert Barton Grossman,jain-hua zhouJain-Hua Zhou,lanlan shenLanlan Shen,jolanta bondarukJolanta Bondaruk,saira s ahmedSaira S Ahmed,susmita samantaSusmita Samanta,philippe spiessPhilippe Spiess,xifeng wuXifeng Wu,slawomir filipekSlawomir Filipek,david mcconkeyDavid McConkey,menashe bar-eliMenashe Bar-Eli,jean-pierre issaJean-Pierre Issa,william f benedictWilliam F Benedict,bogdan czerniakBogdan Czerniak,

    We used human bladder cancer as a model system and the whole-organ histologic and genetic mapping strategy to identify clonal genetic hits associated with growth advantage, tracking the evolution of bladder cancer from intraurothelial precursor lesions. Six putative chromosomal regions critical for clonal expansion of intraurothelial neoplasia and development of bladder cancer were identified by using this approach. Focusing on one of the regions, which includes the model tumor suppressor RB1, we performed allelotyping of single-nucleotide polymorphic sites and identified a 1.34-Mb segment around RB1 characterized by a loss of polymorphism associated with the initial expansion of in situ neoplasia. This segment contains several positional candidate genes referred to by us as forerunner genes that may contribute to such expansion. We subsequently concentrated our efforts on the two neighbor genes flanking RB1, namely ITM2B and CHC1L, as well as P2RY5, which is located inside RB1. Here, we report that ITM2B and P2RY5 modulated cell survival and were silenced by methylation or point mutations, respectively, and thus by functional loss may contribute to the growth advantage of neoplasia. We also show that homozygous inactivation of P2RY5 was antecedent to the loss of RB1 during tumor development, and that nucleotide substitutions in P2RY5 represent a cancer predisposing factor.

    Forerunner genes contiguous to RB1 contribute to the development of in situ neoplasia. Publishing Authors By Initials

    s leeS Lee,j jeongJ Jeong,t majewskiT Majewski,se schererSE Scherer,ms kimMS Kim,t tuziakT Tuziak,ks tangKS Tang,k baggerlyK Baggerly,hb grossmanHB Grossman,jh zhouJH Zhou,l shenL Shen,j bondarukJ Bondaruk,ss ahmedSS Ahmed,s samantaS Samanta,p spiessP Spiess,x wuX Wu,s filipekS Filipek,d mcconkeyD McConkey,m bar-eliM Bar-Eli,jp issaJP Issa,wf benedictWF Benedict,b czerniakB Czerniak,

    For similar neoplasms: neoplasms by site: urogenital neoplasms: urologic neoplasms: urinary bladder neoplasms research abstracts see: neoplasms: neoplasms by site: urogenital neoplasms: urologic neoplasms: urinary bladder neoplasms research

    PUBMED ID PMID:

    MEDLINE DATE:

    Forerunner genes contiguous to RB1 contribute to the development of in situ neoplasia. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Proceedings of the National Academy of Sciences of

    VOLUME: 104

    Page Numbers: 13732-7

    Journal Abbreviation: Proc. Natl. Acad. Sci. U.S.A.

    ISSN: 0027-8424

    DAY: 16

    MONTH: 08

    YEAR: 2007

    Forerunner genes contiguous to RB1 contribute to the development of in situ neoplasia. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7505876

    Forerunner genes contiguous to RB1 contribute to the development of in situ neoplasia. Keywords Mesh Terms:

    KEYWORDS: Urinary Bladder Neoplasms

    MESH TERMS: genetics

    Chemical & Substance for Abstract: Forerunner genes contiguous to RB1 contribute to the development of in situ neoplasia. Information

    Substance Name: Retinoblastoma Protein

    Registry Number: 0

    Grant and Affiliation Information for Forerunner genes contiguous to RB1 contribute to the development of in situ neoplasia.

    AFFILIATION: Department of Pathology, University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCI

    GRANT: U01CA85078

    ACRONYM: CA

    MEDLINETA: Proc Natl Acad Sci U S A

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    DATABASENAME:

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    Number Hits: 0

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