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Cellosaurus ch-2879 (CVCL_9921)

[Text version]
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
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
Rosario Gil-Benso, Concha Lopez-Gines, Jose Antonio Lopez-Guerrero, Carmen Carda, Robert C. Callaghan, Samuel Navarro, Jaime Ferrer, Antonio Pellin, Antonio Llombart-Bosch;
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
Laura Ottaviano, Karl-Ludwig Schaefer, Melanie Gajewski, Wolfgang Huckenbeck, Stefan E. Baldus, Uwe Rogel, Carlos Mackintosh, Enrique de Alava, Ola Myklebost, Stine Henrichson Kresse, Leonardo Andres Meza-Zepeda ...Show all 18 authors... , Massimo Serra, Anne-Marie Cleton-Jansen, Pancras Cornelis Wilhelmus Hogendoorn, Horst Buerger, Thomas Aigner, Helmut Erich Gabbert, Christopher Poremba; Show fewer authors
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; PMCID=PMC3427908
Twinkal Marfatia, Ronald van Eijk, Pio d'Adamo, Maayke A.J.H. van Ruler, Marieke Lydia Kuijjer, Jan Oosting, Anne-Marie Cleton-Jansen, Jolieke G. van Oosterwijk, Sofie L.J. Verbeke, Danielle Meijer, Tom van Wezel ...Show all 27 authors... , Karolin H. Nord, Luca Sangiorgi, Berkin Toker, Bernadette Liegl-Atzwanger, Mikel San-Julian, Raf Sciot, Nisha Limaye, Lars-Gunnar Kindblom, Soeren Daugaard, Catherine Godfraind, Laurence M. Boon, Miikka Vikkula, Kyle C. Kurek, Karoly Szuhai, Pim J. French, Judith V.M.G. Bovee; Show fewer authors
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 update19-Dec-2024
Version number21