Table 1.
GIST cell-lines a characteristics
Origin | KIT mutations and other characteristics | Growth mediumb | |
---|---|---|---|
GIST48 | GIST primary/patientc | Primary, homozygous KIT exon 11 (V560D) mutation; secondary, heterozygous KIT exon 17 (D820Ad) mutation. | IMDM + 15% FBS |
GIST48B | Subline of GIST48 | Retains primary mutation (KIT V560D) in all cells; nearly undetectable KIT transcript and protein; secondary, heterozygous KIT exon 17 (D820Ad) mutation; keeps downstream KIT signaling active |
IMDM + 15% FBS |
Notes: aKindly provided by Dr Fletcher (Department of Pathology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA); breagents purchased from Thermo Fisher Scientific (Waltham, MA); cestablished from a GIST patient that had progressed after initial response to imatinib therapy; dlocated in the kinase-activation loop, confers resistance to imatinib and sunitinib.
Abbreviations: IMDM, Iscove's Modified Dulbecco's Medium; FBS, Fetal Bovine Serum.