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T25
HT-1080/HT-1080细胞系/HT-1080细胞株/HT-1080人纤维肉瘤细胞
Cell line name HT-1080
Synonyms Ht-1080; HT 1080; HT1080; HT 1080.T
Accession CVCL_0317
Resource Identification Initiative To cite this cell line use: HT-1080 (RRID:CVCL_0317)
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 3.
Part of: MD Anderson Cell Lines Project.
Part of: Naval Biosciences Laboratory (NBL) collection (transferred to ATCC in 1982).
Population: Caucasian.
Doubling time: 26 hours (PubMed=4132053); ~30 hours (DSMZ=ACC-315).
Microsatellite instability: Stable (MSS) (Sanger).
Omics: Deep exome analysis.
Omics: Deep quantitative proteome analysis.
Omics: DNA methylation analysis.
Omics: Protein expression by reverse-phase protein arrays.
Omics: SNP array analysis.
Omics: Transcriptome analysis by microarray.
Omics: Transcriptome analysis by RNAseq.
Misspelling: HT1180; Note=Occasionally.
Derived from site: In situ; Bone, pelvis, acetabulum; UBERON=UBERON_0001269.
PubMed=3335022
Alley M.C., Scudiero D.A., Monks A., Hursey M.L., Czerwinski M.J., Fine D.L., Abbott B.J., Mayo J.G., Shoemaker R.H., Boyd M.R.
Feasibility of drug screening with panels of human tumor cell lines using a microculture tetrazolium assay.
Cancer Res. 48:589-601(1988)
PubMed=3413074; DOI=10.1073/pnas.85.16.6042; PMCID=PMC281901
Pereira-Smith O.M., Smith J.R.
Genetic analysis of indefinite division in human cells: identification of four complementation groups.
Proc. Natl. Acad. Sci. U.S.A. 85:6042-6046(1988)
PubMed=11416159; DOI=10.1073/pnas.121616198; PMCID=PMC35459
Masters J.R.W., Thomson J.A., Daly-Burns B., Reid Y.A., Dirks W.G., Packer P., Toji L.H., Ohno T., Tanabe H., Arlett C.F., Kelland L.R., Harrison M., Virmani A.K., Ward T.H., Ayres K.L., Debenham P.G.
Short tandem repeat profiling provides an international reference standard for human cell lines.
Proc. Natl. Acad. Sci. U.S.A. 98:8012-8017(2001)
PubMed=11668190; DOI=10.1177/002215540104901105
Quentmeier H., Osborn M., Reinhardt J., Zaborski M., Drexler H.G.
Immunocytochemical analysis of cell lines derived from solid tumors.
J. Histochem. Cytochem. 49:1369-1378(2001)
PubMed=12068308; DOI=10.1038/nature00766
Davies H.R., Bignell G.R., Cox C., Stephens P.J., Edkins S., Clegg S., Teague J.W., Woffendin H., Garnett M.J., Bottomley W., Davis N., Dicks E., Ewing R., Floyd Y., Gray K., Hall S., Hawes R., Hughes J., Kosmidou V., Menzies A., Mould C., Parker A., Stevens C., Watt S., Hooper S., Wilson R., Jayatilake H., Gusterson B.A., Cooper C.S., Shipley J.M., Hargrave D., Pritchard-Jones K., Maitland N.J., Chenevix-Trench G., Riggins G.J., Bigner D.D., Palmieri G., Cossu A., Flanagan A.M., Nicholson A., Ho J.W.C., Leung S.Y., Yuen S.T., Weber B.L., Seigler H.F., Darrow T.L., Paterson H.F., Marais R., Marshall C.J., Wooster R., Stratton M.R., Futreal P.A.
Mutations of the BRAF gene in human cancer.
Nature 417:949-954(2002)
CLPUB00698
van Bokhoven A.
Models for prostate cancer. Molecular characterization and critical appraisal of human prostate carcinoma cell lines.
Thesis PhD (2004); Katholieke Universiteit Nijmegen; Nijmegen; Netherlands
PubMed=17254797; DOI=10.1016/j.biologicals.2006.10.001
Azari S., Ahmadi N., Jeddi-Tehrani M., Shokri F.
Profiling and authentication of human cell lines using short tandem repeat (STR) loci: report from the National Cell Bank of Iran.
Biologicals 35:195-202(2007)
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=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)
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文献和实验*发表【中文论文】请标注：由博辉生物科技（广州）有限公司提供； *发表【英文论文】请标注：From Bohui Biological Technology (Guangzhou) Co., Ltd.
做好准备工作之后，先把旧的培养基倒掉。再用PBS洗两遍，然后加0.05%胰酶/EDTA，剂量根据培养瓶大小定，一般是25cm 2 的瓶子大约0.8-1ml，轻摇10——15秒，使消化液均匀覆盖瓶底即可，再倒掉。置培养箱3-5分钟(看消化效果而定)，等大部分细胞呈流沙状滑落时，即加入培养基终止消化，一般以1:5左右的比例传代(视计数结果和看细胞长满的程度而定)。这种方法养比较顽强的细胞很好，既节省步骤，也降低了离心和较长时间消化对细胞带来的损伤，其实大家也可以试试用这种方法养别的细胞。主要做
重大突破！甘波谊团队 Nature 首次报道第三种铁死亡抑制机制，提供抗癌新思路
）使细胞对 GPX4 抑制剂更加敏感；然而，添加尿苷并不影响细胞对 GPX4 抑制剂的敏感性。 图片来源：NatureDHO 和 OA 分别是 DHODH 反应的底物和产物，DHO 和 OA 对铁死亡有着相反的影响，提示 DHODH 可能对于铁死亡有着调节作用。作者发现抑制 DHODH 可诱导 GPX4 低表达的细胞（如 NCI-H226）发生铁死亡；对于 GPX4 高表达的细胞（如 HT-1080），抑制 DHODH 不能显著诱导铁死亡的发生，但能使细胞对铁死亡诱导剂变得更加敏感，而敲除 GPX
【思路解读】一篇 10 分 SCI 文章，教你入手「铁死亡」的国自然课题设计思路
-MB-453 和 BT474 细胞对 RSL3 诱导的「铁死亡」敏感，而 RICTOR（mTORC2 的组成部分）沉默不能。 图片来源：参考文献 5 Figure 2 3. NRF2 不是 mTORC1 抑制「铁死亡」的主要介质 随着研究的不断进行，研究者还发现 RSL3 诱导的 NRF2 积聚可以被 Torin 治疗所消融，但 HT1080 细胞中的 NRF2 基因敲除只是温和地增强了 erastin（xc-半胱氨酸/谷氨酸逆向转运蛋白系统的化学抑制剂）诱导的铁死亡，而对 RSL3 诱导的「铁
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