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Models representing type I and type II human endometrial cancers: Ishikawa H and Hec50co cells.

Models representing type I and type II human endometrial cancers: Ishikawa H and Hec50co cells. Research Abstract Details 

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  • Models representing type I and type II human endometrial cancers: Ishikawa H and Hec50co cells. Abstract Text:

    lina albitarLina Albitar,gavin pickettGavin Pickett,marilee morganMarilee Morgan,suzy daviesSuzy Davies,kimberly k leslieKimberly K Leslie,

    OBJECTIVE: Endometrial cancer models are critical to the advancement of investigation, and Ishikawa H and Hec50co cells have been used as research tools. The purpose of these studies is to verify the degree to which these commonly used cell models share the molecular characteristics of the two major in vivo endometrial cancer subtypes, I and II. METHODS: The studies reported include an analysis of pathologic features, tumor suppressor mutations, detailed karyotyping, and cell cycle regulation. RESULTS: Ishikawa H cells are hormone responsive and have lost PTEN expression. In addition they have lost RB1 expression due to a deletion in exon 9. Hec50co cells have lost p53 expression due to a deletion at the junction of exon 6 and intron 6-7. Compared to Ishikawa H cells, Hec50co cells harbor many more chromosomal rearrangements (29 versus seven), and the doubling time is more rapid. The percent of cells in each phase of the cell cycle is reported and linked to cell cycle regulators. CONCLUSION: We present extensive data indicating that Ishikawa H cells are excellent models for type I endometrial cancers, and Hec50co cells faithfully replicate the molecular characteristics of type II endometrial cancers. These studies allow testing of new therapeutic regimens using appropriate cell models.

    Models representing type I and type II human endometrial cancers: Ishikawa H and Hec50co cells. Publishing Authors By Initials

    l albitarL Albitar,g pickettG Pickett,m morganM Morgan,s daviesS Davies,kk leslieKK Leslie,

    For similar proteins: dna-binding proteins: tumor suppressor protein p53 research abstracts see: proteins: dna-binding proteins: tumor suppressor protein p53 research

    PUBMED ID PMID:

    MEDLINE DATE:

    Models representing type I and type II human endometrial cancers: Ishikawa H and Hec50co cells. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Gynecologic oncology

    VOLUME: 106

    Page Numbers: 52-64

    Journal Abbreviation: Gynecol. Oncol.

    ISSN: 0090-8258

    DAY: 8

    MONTH: 05

    YEAR: 2007

    Models representing type I and type II human endometrial cancers: Ishikawa H and Hec50co cells. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 365304

    Models representing type I and type II human endometrial cancers: Ishikawa H and Hec50co cells. Keywords Mesh Terms:

    KEYWORDS: Tumor Suppressor Protein p53

    MESH TERMS: genetics

    Chemical & Substance for Abstract: Models representing type I and type II human endometrial cancers: Ishikawa H and Hec50co cells. Information

    Substance Name: Tumor Suppressor Protein p53

    Registry Number: 0

    Grant and Affiliation Information for Models representing type I and type II human endometrial cancers: Ishikawa H and Hec50co cells.

    AFFILIATION: Obstetrics and Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, The Cancer Research and Treatment Center, The University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCI

    GRANT: R01CA99908-1

    ACRONYM: CA

    MEDLINETA: Gynecol Oncol

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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