Skip to main content

Table 3 Effect of the combination between the USP1/UAF1 inhibitor pimozide with the chemotherapy agent cisplatin in a panel of NSCLC cell lines

From: USP1 deubiquitinase: cellular functions, regulatory mechanisms and emerging potential as target in cancer therapy

Cell line

Cisplatin

Pimozide

Ratio C:P

C.I.

Combination effect

IC50(μM)

IC50(μM)

H322 (s)

1.6

11.6

1:7

1.3

Antagonistic

SKLU-1 (s)

2.4

13.7

1:6

1.2

Antagonistic

SW1573 (s)

4.4

10.5

1:2

2.0

Antagonistic

H522 (s)

5.0

10.8

1:2

0.9

Additive

H1299 (r)

7.5

7.0

1:1

0.6

Synergistic

H1703 (r)

8.8

5.0

2:1

1.0

Additive

H520 (r)

13.7

8.7

2:1

1.1

Additive

  1. The IC50 value for cisplatin and pimozide was calculated for each cell line as described in Figure 4. Cell lines were classified as “cisplatin-sensitive” (s) if their IC50 for this drug was below the mean value of the panel (6.2 μM), or as “cisplatin-resistant” (r) if their IC50 was above the mean. Treatment with the two drugs in combination was carried out using a constant ratio cisplatin:pimozide (Ratio C:P) that was individually established for each cell line as the ratio of the IC50 values for each single drug. The combination index (C.I) value was calculated at a full range of Fa values using CalcuSyn, as described in Figure 4. We calculated the final C.I. value for each experiment as the average C.I. at Fa = 0.5, 0.75 and 0.9. At least three independent experiments per cell line were carried out, and the C.I. value indicated in the Table represents the mean of the final C.I. values of these experiments. According to the C.I., the nature of the interaction between the drugs (Combination effect) was classified as synergistic (C.I. < 0.8), additive (0.8 < C.I. < 1.2) or antagonistic (C.I. > 1.2).