Table 1.
Cell Line | Chromosomal Alteration | NMA* | p53 | Alk | IC50 (ng/ml) | IC80 (ng/ml) | Ref |
---|---|---|---|---|---|---|---|
IMR32 | 1p LOH | + | wt | wt | 1 | 2 | 22 |
SK-N-BE(2) | 1p LOH, t(3,17)(p21,q21) | + | mt | wt | 6.3 | 30 | 18 |
SMS-KCNR | 1p LOH, t(17,20)(p21,q13) | + | wt | mt, R1275Q | 2 | 5 | 17 |
SK-N-AS | 1p del, 1p(36.33) | − | wt | wt | 1.8 | 30 | 20 |
SH-SY5Y | 1p LOH | − | wt | mt, F1174L | 5 | 30 | 19 |
SH-SHEP | 1p LOH | − | wt | mt, F1174L | 1 | 4 | 22 |
LA1–15N | 1p LOH | + | mt | mt, F1174L | 1.2 | 10 | 21 |
NMA-MYCN amplified; LOH= loss of hterozygosity; wt=wild-type; mt=mutant