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Cellosaurus ch-2879 (CVCL_9921)

Cell line name ch-2879
Synonyms CH-2879; CH2879
Accession CVCL_9921
Resource Identification Initiative To cite this cell line use: ch-2879 (RRID:CVCL_9921)
Comments Derived from site: In situ; Bone, rib; UBERON=UBERON_0002228.
Sequence variations
  • Gene deletion; HGNC; 1787; CDKN2A; Zygosity=Homozygous (PubMed=19787792).
  • Mutation; HGNC; 5382; IDH1; None_reported; -; Zygosity=- (PubMed=22057234).
  • Mutation; HGNC; 5383; IDH2; None_reported; -; Zygosity=- (PubMed=22057234).
  • Mutation; HGNC; 11998; TP53; None_reported; -; Zygosity=- (PubMed=19787792).
Disease Primary central chondrosarcoma (NCIt: C7155)
Chondrosarcoma (ORDO: Orphanet_55880)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 35Y
Category Cancer cell line
STR profile Source(s): PubMed=19787792

Markers:
AmelogeninX
D2S133817
D3S135816
D5S81812
D8S117912
D16S5398,9
D18S5112
D19S43314
D21S1130,32.2
FGA22
SE3332.2
TH018
TPOX10,11
vWA16

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Publications

PubMed=12808123; DOI=10.1097/01.LAB.0000073131.34648.EA
Gil-Benso R., Lopez-Gines C., Lopez-Guerrero J.A., Carda C., Callaghan R.C., Navarro S., Ferrer J., Pellin A., Llombart-Bosch A.
Establishment and characterization of a continuous human chondrosarcoma cell line, ch-2879: comparative histologic and genetic studies with its tumor of origin.
Lab. Invest. 83:877-887(2003)

PubMed=19787792; DOI=10.1002/gcc.20717
Ottaviano L., Schaefer K.-L., Gajewski M., Huckenbeck W., Baldus S.E., Rogel U., Mackintosh C., de Alava E., Myklebost O., Kresse S.H., Meza-Zepeda L.A., Serra M., Cleton-Jansen A.-M., Hogendoorn P.C.W., Buerger H., Aigner T., Gabbert H.E., Poremba C.
Molecular characterization of commonly used cell lines for bone tumor research: a trans-European EuroBoNet effort.
Genes Chromosomes Cancer 49:40-51(2010)

PubMed=22057234; DOI=10.1038/ng.1004
Pansuriya T.C., van Eijk R., d'Adamo P., van Ruler M.A.J.H., Kuijjer M.L., Oosting J., Cleton-Jansen A.-M., van Oosterwijk J.G., Verbeke S.L.J., Meijer D., van Wezel T., Nord K.H., Sangiorgi L., Toker B., Liegl-Atzwanger B., San-Julian M., Sciot R., Limaye N., Kindblom L.-G., Daugaard S., Godfraind C., Boon L.M., Vikkula M., Kurek K.C., Szuhai K., French P.J., Bovee J.V.M.G.
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome.
Nat. Genet. 43:1256-1261(2011)

Cross-references
Encyclopedic resources Wikidata; Q54811597
Polymorphism and mutation databases Cosmic; 1602477
Cosmic; 1992324
IARC_TP53; 27034
Entry history
Entry creation06-Jun-2012
Last entry update29-Jun-2023
Version number20