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HCC1806细胞

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      T25

    HCC1806/HCC1806细胞系/HCC1806细胞株/HCC1806人乳腺鳞状癌细胞

    Cell line name HCC1806

    Synonyms Hcc1806; HCC-1806; Hamon Cancer Center 1806

    Accession CVCL_1258

    Resource Identification Initiative To cite this cell line use: HCC1806 (RRID:CVCL_1258)

    Comments Group: Triple negative breast cancer (TNBC) cell line.

    Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE).

    Part of: COSMIC cell lines project.

    Part of: JWGray breast cancer cell line panel.

    Part of: ICBP43 breast cancer cell line panel.

    Part of: KuDOS 95 cell line panel.

    Part of: MD Anderson Cell Lines Project.

    Population: African American.

    Doubling time: 36.66 hours (JWGray panel).

    Microsatellite instability: Stable (MSS) (Sanger).

    Omics: Array-based CGH.

    Omics: CNV analysis.

    Omics: CRISPR phenotypic screen.

    Omics: Deep exome analysis.

    Omics: Deep quantitative proteome analysis.

    Omics: DNA methylation analysis.

    Omics: CTCF ChIP-seq epigenome analysis.

    Omics: H2A.Z ChIP-seq epigenome analysis.

    Omics: H3K27ac ChIP-seq epigenome analysis.

    Omics: H3K27me3 ChIP-seq epigenome analysis.

    Omics: H3K4me1 ChIP-seq epigenome analysis.

    Omics: H3K4me2 ChIP-seq epigenome analysis.

    Omics: H3K4me3 ChIP-seq epigenome analysis.

    Omics: H3K9ac ChIP-seq epigenome analysis.

    Omics: H4K20me1 ChIP-seq epigenome analysis.

    Omics: Pol2 ChIP-seq epigenome analysis.

    Omics: miRNA expression profiling.

    Omics: Protein expression by reverse-phase protein arrays.

    Omics: SNP array analysis.

    Omics: Transcriptome analysis by microarray.

    Omics: Transcriptome analysis by RNAseq.

    Derived from site: In situ; Breast; UBERON=UBERON_0000310.

    PubMed=9833771; DOI=10.1002/(SICI)1097-0215(19981209)78:6<766::AID-IJC15>3.0.CO;2-L

    Gazdar A.F., Kurvari V., Virmani A.K., Gollahon L.S., Sakaguchi M., Westerfield M., Kodagoda D.R., Stasny V., Cunningham H.T., Wistuba I.I., Tomlinson G.E., Tonk V., Ashfaq R., Leitch A.M., Minna J.D., Shay J.W.

    Characterization of paired tumor and non-tumor cell lines established from patients with breast cancer.

    Int. J. Cancer 78:766-774(1998)

     

    PubMed=9865903

    Wistuba I.I., Behrens C., Milchgrub S., Syed S., Ahmadian M., Virmani A.K., Kurvari V., Cunningham T.H., Ashfaq R., Minna J.D., Gazdar A.F.

    Comparison of features of human breast cancer cell lines and their corresponding tumors.

    Clin. Cancer Res. 4:2931-2938(1998)

     

    PubMed=11314036; DOI=10.1038/sj.onc.1204211

    Forgacs E., Wren J.D., Kamibayashi C., Kondo M., Xu X.L., Markowitz S.D., Tomlinson G.E., Muller C.Y., Gazdar A.F., Garner H.R., Minna J.D.

    Searching for microsatellite mutations in coding regions in lung, breast, ovarian and colorectal cancers.

    Oncogene 20:1005-1009(2001)

     

    PubMed=12353263; DOI=10.1002/gcc.10107

    Popovici C., Basset C., Bertucci F., Orsetti B., Adelaide J., Mozziconacci M.-J., Conte N., Murati A., Ginestier C., Charafe-Jauffret E., Ethier S.P., Lafage-Pochitaloff M., Theillet C., Birnbaum D., Chaffanet M.

    Reciprocal translocations in breast tumor cell lines: cloning of a t(3;20) that targets the FHIT gene.

    Genes Chromosomes Cancer 35:204-218(2002)

     

    PubMed=12800145; DOI=10.1002/gcc.10218

    Adelaide J., Huang H.-E., Murati A., Alsop A.E., Orsetti B., Mozziconacci M.-J., Popovici C., Ginestier C., Letessier A., Basset C., Courtay-Cahen C., Jacquemier J., Theillet C., Birnbaum D., Edwards P.A.W., Chaffanet M.

    A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 gene.

    Genes Chromosomes Cancer 37:333-345(2003)

     

    PubMed=19582160; DOI=10.1371/journal.pone.0006146; PMCID=PMC2702084

    Kao J., Salari K., Bocanegra M., Choi Y.-L., Girard L., Gandhi J., Kwei K.A., Hernandez-Boussard T., Wang P., Gazdar A.F., Minna J.D., Pollack J.R.

    Molecular profiling of breast cancer cell lines defines relevant tumor models and provides a resource for cancer gene discovery.

    PLoS ONE 4:E6146-E6146(2009)

     

    PubMed=20070913; DOI=10.1186/1471-2407-10-15; PMCID=PMC2836299

    Tsuji K., Kawauchi S., Saito S., Furuya T., Ikemoto K., Nakao M., Yamamoto S., Oka M., Hirano T., Sasaki K.

    Breast cancer cell lines carry cell line-specific genomic alterations that are distinct from aberrations in breast cancer tissues: comparison of the CGH profiles between cancer cell lines and primary cancer tissues.

    BMC Cancer 10:15.1-15.10(2010)

     

    PubMed=20164919; DOI=10.1038/nature08768; PMCID=PMC3145113

    Bignell G.R., Greenman C.D., Davies H.R., Butler A.P., Edkins S., Andrews J.M., Buck G., Chen L., Beare D., Latimer C., Widaa S., Hinton J., Fahey C., Fu B.-Y., Swamy S., Dalgliesh G.L., Teh B.T., Deloukas P., Yang F.-T., Campbell P.J., Futreal P.A., Stratton M.R.

    Signatures of mutation and selection in the cancer genome.

    Nature 463:893-898(2010)

     

    PubMed=20679594; DOI=10.1093/jnci/djq279; PMCID=PMC2935474

    Gazdar A.F., Girard L., Lockwood W.W., Lam W.L., Minna J.D.

    Lung cancer cell lines as tools for biomedical discovery and research.

    J. Natl. Cancer Inst. 102:1310-1321(2010)

     

    PubMed=21778573; DOI=10.3233/BD-2010-0307; PMCID=PMC3532890

    Chavez K.J., Garimella S.V., Lipkowitz S.

    Triple negative breast cancer cell lines: one tool in the search for better treatment of triple negative breast cancer.

    Breast Dis. 32:35-48(2010)

     

    PubMed=21603256; DOI=10.4137/BCBCR.S7087; PMCID=PMC3091405

    Neves L.A.H., Ingram L.M., Davis M.B.

    The characterization of cell line CRL-2335 as a basal-like breast carcinoma model.

    Breast Cancer (Auckl.) 5:67-72(2011)

     

    PubMed=22460905; DOI=10.1038/nature11003; PMCID=PMC3320027

    Barretina J.G., Caponigro G., Stransky N., Venkatesan K., Margolin A.A., Kim S., Wilson C.J., Lehar J., Kryukov G.V., Sonkin D., Reddy A., Liu M., Murray L., Berger M.F., Monahan J.E., Morais P., Meltzer J., Korejwa A., Jane-Valbuena J., Mapa F.A., Thibault J., Bric-Furlong E., Raman P., Shipway A., Engels I.H., Cheng J., Yu G.-Y.K., Yu J.-J., Aspesi P. Jr., de Silva M., Jagtap K., Jones M.D., Wang L., Hatton C., Palescandolo E., Gupta S., Mahan S., Sougnez C., Onofrio R.C., Liefeld T., MacConaill L.E., Winckler W., Reich M., Li N.-X., Mesirov J.P., Gabriel S.B., Getz G., Ardlie K., Chan V., Myer V.E., Weber B.L., Porter J., Warmuth M., Finan P., Harris J.L., Meyerson M.L., Golub T.R., Morrissey M.P., Sellers W.R., Schlegel R., Garraway L.A.

    The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.

    Nature 483:603-607(2012)

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      (MCF-7和HCC1806) 转移疗效的。       研究者通过比较划痕处理后细胞迁移的趋势和速度,发现Maestro Z系统能够轻松地将两种肿瘤细胞系的差别区分开来。HCC1806细胞相对于MCF-7而言有更强的迁移能力, 这点能够和临床上观察到的三阴乳腺癌肿瘤细胞的高转移能力相呼应。此外,她们还发现MaestroZ系统对于不同抗转移MCP在作用效应和动态上的微小差别很敏感,证实了它在评估抗转移治疗疗效方面的价值。若要了解更多,可参考:(page_2 - (axionbio.cn))

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