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. 2019 Jul 5;11:6229–6244. doi: 10.2147/CMAR.S189661

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.