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A549细胞

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    【A549】A549细胞/A549细胞/A549人非小细胞肺癌细胞Cell line name A-549

    Synonyms A 549; A549; NCI-A549; A549/ATCC; A549 ATCC; A549ATCC; hA549

    Accession CVCL_0023

    Secondary accession CVCL_H249

    Resource Identification Initiative To cite this cell line use: A-549 (RRID:CVCL_0023)

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

    Part of: COSMIC cell lines project.

    Part of: ENCODE project common cell types; tier 2.

    Part of: JFCR39 cancer cell line panel.

    Part of: KuDOS 95 cell line panel.

    Part of: MD Anderson Cell Lines Project.

    Part of: Naval Biosciences Laboratory (NBL) collection (transferred to ATCC in 1982).

    Part of: NCI-60 cancer cell line panel.

    Part of: NCI-7 clinical proteomics reference material cell line panel.

    Registration: International Depositary Authority, Japanese National Institute of Bioscience and Human-Technology, Agency of Industrial Science and Technology; FERM BP-2000.

    Population: Caucasian.

    Characteristics: Expresses HPRT1 at the surface of the cell membrane (PubMed=28408844).

    Virology: Highly susceptible to infection by Zika virus (ZIKV) (PubMed=29468137).

    Doubling time: 18 hours (Note=In RPMI 1640 + 10% FBS), 37 hours (Note=In ACL-3), 36 hours (Note=In ACL-3+BSA) (PubMed=3940644); 27.0 hours (PubMed=8286010); 22 hours (PubMed=25984343); 23.9 hours (PubMed=29681454); 27 hours (Note=From cell counting), 27 hours (Note=From absorbance) (DOI=10.5897/IJBMBR2013.0154); 26.08 hours (PubMed=35976051); ~28 hours (CLS=300114); ~40 hours (DSMZ=ACC-107); 22.9 hours (NCI-DTP=A549).

    Microsatellite instability: Stable (MSS) (PubMed=12661003; Sanger).

    Omics: Acetylation analysis by proteomics.

    Omics: Array-based CGH.

    Omics: CNV analysis.

    Omics: CTCF ChIP-seq epigenome analysis.

    Omics: H3K4me3 ChIP-seq epigenome analysis.

    Omics: H3K9ac ChIP-seq epigenome analysis.

    Omics: CRISPR phenotypic screen.

    Omics: Deep antibody staining analysis.

    Omics: Deep exome analysis.

    Omics: Deep membrane proteome analysis.

    Omics: Deep phosphoproteome analysis.

    Omics: Deep proteome analysis.

    Omics: Deep quantitative proteome analysis.

    Omics: DNA methylation analysis.

    Omics: Fluorescence phenotype profiling.

    Omics: lncRNA expression profiling.

    Omics: Metabolome analysis.

    Omics: Protein expression by reverse-phase protein arrays.

    Omics: Proteome analysis by 2D-DE/MS.

    Omics: shRNA library screening.

    Omics: SNP array analysis.

    Omics: Transcriptome analysis by microarray.

    Omics: Transcriptome analysis by RNAseq.

    Omics: Virome analysis using proteomics.

    Misspelling: A59; PubMed=16354588.

    Misspelling: A594; Note=In abstract of PubMed=18227028.

    Derived from site: In situ; Lung; UBERON=UBERON_0002048.

    PubMed=23856246; DOI=10.1158/0008-5472.CAN-12-3342; PMCID=PMC4893961

    Abaan O.D., Polley E.C., Davis S.R., Zhu Y.-L.J., Bilke S., Walker R.L., Pineda M.A., Gindin Y., Jiang Y., Reinhold W.C., Holbeck S.L., Simon R.M., Doroshow J.H., Pommier Y., Meltzer P.S.

    The exomes of the NCI-60 panel: a genomic resource for cancer biology and systems pharmacology.

    Cancer Res. 73:4372-4382(2013)

     

    PubMed=23933261; DOI=10.1016/j.celrep.2013.07.018

    Moghaddas Gholami A., Hahne H., Wu Z.-X., Auer F.J., Meng C., Wilhelm M., Kuster B.

    Global proteome analysis of the NCI-60 cell line panel.

    Cell Rep. 4:609-620(2013)

     

    PubMed=24135919; DOI=10.1038/ncomms3617; PMCID=PMC4107456

    Balbin O.A., Prensner J.R., Sahu A., Yocum A., Shankar S., Malik R., Fermin D., Dhanasekaran S.M., Chandler B., Thomas D., Beer D.G., Cao X.-H., Nesvizhskii A.I., Chinnaiyan A.M.

    Reconstructing targetable pathways in lung cancer by integrating diverse omics data.

    Nat. Commun. 4:2617.1-2617.13(2013)

     

    PubMed=24279929; DOI=10.1186/2049-3002-1-20; PMCID=PMC4178206

    Dolfi S.C., Chan L.L.-Y., Qiu J., Tedeschi P.M., Bertino J.R., Hirshfield K.M., Oltvai Z.N., Vazquez A.

    The metabolic demands of cancer cells are coupled to their size and protein synthesis rates.

    Cancer Metab. 1:20.1-20.13(2013)

     

    PubMed=24618588; DOI=10.1371/journal.pone.0091433; PMCID=PMC3950186

    Chernobrovkin A.L., Zubarev R.A.

    Detection of viral proteins in human cells lines by xeno-proteomics: elimination of the last valid excuse for not testing every cellular proteome dataset for viral proteins.

    PLoS ONE 9:E91433-E91433(2014)

     

    PubMed=24670534; DOI=10.1371/journal.pone.0092047; PMCID=PMC3966786

    Varma S., Pommier Y., Sunshine M., Weinstein J.N., Reinhold W.C.

    High resolution copy number variation data in the NCI-60 cancer cell lines from whole genome microarrays accessible through CellMiner.

    PLoS ONE 9:E92047-E92047(2014)

     

    PubMed=25120651; DOI=10.3892/ol.2014.2234; PMCID=PMC4114630

    Suzuki M., Ikeda K., Shiraishi K., Eguchi A., Mori T., Yoshimoto K., Shibata H., Ito T., Baba Y., Baba H.

    Aberrant methylation and silencing of IRF8 expression in non-small cell lung cancer.

    Oncol. Lett. 8:1025-1030(2014)

     

    PubMed=25475639; DOI=10.5731/pdajpst.2014.01027

    Shabram P., Kolman J.L.

    Evaluation of A549 as a new vaccine cell substrate: digging deeper with massively parallel sequencing.

    PDA J. Pharm. Sci. Technol. 68:639-650(2014)

     

    PubMed=25960936; DOI=10.4161/21624011.2014.954893; PMCID=PMC4355981

    Boegel S., Lower M., Bukur T., Sahin U., Castle J.C.

    A catalog of HLA type, HLA expression, and neo-epitope candidates in human cancer cell lines.

    OncoImmunology 3:e954893.1-e954893.12(2014)

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    *发表【英文论文】请标注:From Shanghai EK-Bioscience Biotechnology Co., Ltd.

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