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T25
SK-N-BE(2)/SK-N-BE(2)细胞系/SK-N-BE(2)细胞株/SK-N-BE(2)人神经母细胞瘤细胞
Cell line name SK-N-BE(2)
Synonyms SK-N-BE2; SK-N-BE-2; SKNBE(2); SKNBE-2; SKNBE2; SK-N-BE; SKNBE
Accession CVCL_0528
Resource Identification Initiative To cite this cell line use: SK-N-BE(2) (RRID:CVCL_0528)
Comments Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE).
From: Memorial Sloan Kettering Cancer Center; New York; USA.
Registration: Memorial Sloan Kettering Cancer Center Office of Technology Development; SK1980-530.
Population: Caucasian.
Characteristics: Substrate-adherent type (S-type) (PubMed=15720811).
Doubling time: 27 hours (PubMed=29704); ~36 hours (DSMZ=ACC-632).
Omics: Array-based CGH.
Omics: Deep exome analysis.
Omics: Deep quantitative phosphoproteome analysis.
Omics: Deep tyrosine phosphoproteome analysis.
Omics: DNA methylation analysis.
Omics: Metabolome analysis.
Omics: SNP array analysis.
Omics: Transcriptome analysis by microarray.
Omics: Transcriptome analysis by RNAseq.
Derived from site: Metastatic; Bone marrow; UBERON=UBERON_0002371.
DOI=10.1016/B978-0-12-333530-2.50006-X
Israel M.A., Thiele C.J.
Tumor cell lines of the peripheral nervous system.
(In book chapter) Atlas of human tumor cell lines; Hay R.J., Park J.-G., Gazdar A.F. (eds.); pp.43-78; Academic Press; New York; USA (1994)
PubMed=7838528
Cheng N.C., Van Roy N., Chan A., Beitsma M., Westerveld A., Speleman F., Versteeg R.
Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35-36 region, only one of which is associated with N-myc amplification.
Oncogene 10:291-297(1995)
DOI=10.1007/0-306-46872-7_2
Thiele C.J.
Neuroblastoma.
(In book chapter) Human cell culture. Vol. 1. Cancer cell lines part 1; Masters J.R.W., Palsson B.O. (eds.); pp.21-53; Kluwer Academic Publishers; New York; USA (1999)
PubMed=11507071
Keshelava N., Zuo J.J., Chen P., Waidyaratne S.N., Luna M.C., Gomer C.J., Triche T.J., Reynolds C.P.
Loss of p53 function confers high-level multidrug resistance in neuroblastoma cell lines.
Cancer Res. 61:6185-6193(2001)
PubMed=11550280; DOI=10.1002/gcc.1174
Van Roy N., Van Limbergen H., Vandesompele J., Van Gele M., Poppe B., Salwen H.R., Laureys G., Manoel N., De Paepe A., Speleman F.
Combined M-FISH and CGH analysis allows comprehensive description of genetic alterations in neuroblastoma cell lines.
Genes Chromosomes Cancer 32:126-135(2001)
PubMed=15720811; DOI=10.1593/neo.04310; PMCID=PMC1531688
Walton J.D., Kattan D.R., Thomas S.K., Spengler B.A., Guo H.-F., Biedler J.L., Cheung N.-K.V., Ross R.A.
Characteristics of stem cells from human neuroblastoma cell lines and in tumors.
Neoplasia 6:838-845(2004)
PubMed=15892104; DOI=10.1002/gcc.20198
Mosse Y.P., Greshock J., Margolin A.A., Naylor T., Cole K.A., Khazi D., Hii G., Winter C., Shahzad S., Asziz M.U., Biegel J.A., Weber B.L., Maris J.M.
High-resolution detection and mapping of genomic DNA alterations in neuroblastoma.
Genes Chromosomes Cancer 43:390-403(2005)
PubMed=16822308; DOI=10.1186/1471-2407-6-177; PMCID=PMC1533846
Dam V., Morgan B.T., Mazanek P., Hogarty M.D.
Mutations in PIK3CA are infrequent in neuroblastoma.
BMC Cancer 6:177.1-177.10(2006)
PubMed=20215515; DOI=10.1158/0008-5472.CAN-09-3458; PMCID=PMC2881662
Rothenberg S.M., Mohapatra G., Rivera M.N., Winokur D., Greninger P., Nitta M., Sadow P.M., Sooriyakumar G., Brannigan B.W., Ulman M.J., Perera R.M., Wang R., Tam A., Ma X.-J., Erlander M., Sgroi D.C., Rocco J.W., Lingen M.W., Cohen E.E.W., Louis D.N., Settleman J., Haber D.A.
A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers.
Cancer Res. 70:2158-2164(2010)
PubMed=20631050; DOI=10.1101/gr.106252.110; PMCID=PMC2928498
Storlazzi C.T., Lonoce A., Guastadisegni M.C., Trombetta D., D'Addabbo P., Daniele G., L'Abbate A., Macchia G., Surace C., Kok K., Ullmann R., Purgato S., Palumbo O., Carella M., Ambros P.F., Rocchi M.
Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure.
Genome Res. 20:1198-1206(2010)
PubMed=20655465; DOI=10.1016/j.cell.2010.06.004; PMCID=PMC2913027
Holzel M., Huang S.-D., Koster J., Ora I., Lakeman A., Caron H.N., Nijkamp W., Xie J., Callens T., Asgharzadeh S., Seeger R.C., Messiaen L.M., Versteeg R., Bernards R.
NF1 is a tumor suppressor in neuroblastoma that determines retinoic acid response and disease outcome.
Cell 142:218-229(2010)
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文献和实验*发表【中文论文】请标注：由上海酶研生物科技有限公司提供；
*发表【英文论文】请标注：From Shanghai EK-Bioscience Biotechnology Co., Ltd.
胞苷一磷酸-N－乙酰神经氨酸cytidine monophosphate N－acetylneuraminic acid
简写为 CMP－ N-乙酰神经氨酸。 N-乙酰神经氨酸是一种多糖，特别是其作为分泌在动物细胞表面或细胞外的糖蛋白质和糖脂质末端的糖成分而广泛地分布着。其末端残基是通过总称为唾液酸转移酶（ sialyltransfer－ ase）的酶从这种 CMP－ N-乙酰神经氨酸转移而来。一般具有这种机能的糖核苷酸，是糖结合到核苷二磷酸上，但仅 CMP－ N-乙酰神经氨酸是例外。 CMP－ N-乙酰神经氨酸是通过专性的焦磷酸化酶的作用从 CTP和 N-乙酰神经氨酸进行生物合成的。极
刚开始养SK-BR-3时，细胞状态不是很好，贴壁也不均匀，于是开始想办法，考虑是不是吹打的不够，或是传得过多，或是其它的什么，后来发现的确如此，细胞的生长状态与传代的方法有很密切的联系。我的传代方法是：以50平方厘米培养瓶为例，待细胞长满瓶底70％－80％1 、吸除或倒掉瓶内旧培养基。2 、PBS 5ml加入培养瓶，轻轻晃动培养瓶，让PBS流遍细胞表面，倒掉。3 、PBS 5ml加入培养瓶重复洗一次，倒掉。4 、加入1ml胰蛋白酶消化液，轻轻摇动培养瓶，使消化液流遍所有细胞表面，然后置37度
许多烟草属（ Nicotiana）植物，虽全身可被感染烟草花叶病病毒，但只有两三个品种如粘毛烟草（ N． glutiosa）和黄花烟草（ N． rustica）的感染细胞会发生坏疽而死亡，而病毒只存在于感染部位的局部病斑，不向全身扩展。感染烟草花叶病毒细胞的坏死，这种性质是受单一显性遗传基因—— N基因支配的。烟草（ N． tabacum）本来不具有 N基因，但与来自具有 N基因的粘毛烟草的双二倍体—— N． diglu- ta杂交后，就能得到具有 N基因的品种。
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