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Table 3 Combination treatment of SSZ and DFMO in SK-N-Be(2)c and LAN-5 cells for 48 h

From: Effect of sulfasalazine on human neuroblastoma: analysis of sepiapterin reductase (SPR) as a new therapeutic target

 

Concentration, IC50 Equivalent

    

NB Cell Line

SSZ

DFMO

Combination Index at 50 % Effect Level

Evaluation at 50 % Effect Level

SSZ IC50 (μM)

DFMO (mM)

SK-N-Be(2)c

0.408

0.425

0.834

slight synergism

54.360

1.800

 

0.223

0.614

0.837

slight synergism

29.640

2.600

 

0.314

0.803

1.117

moderate antagonism

41.740

3.400

 

0.140

0.992

1.132

moderate antagonism

18.700

4.200

 

0.415

1.181

1.595

antagonism

55.180

5.000

LAN-5

0.004

0.207

0.211

strong synergism

1.207

1.200

 

0.173

0.311

0.484

synergism

58.250

1.800

 

0.015

0.466

0.482

synergism

5.152

2.700

 

0.439

0.691

1.130

moderate antagonism

147.900

4.000

 

0.003

1.037

1.039

additive

0.893

6.000

  1. Legend: The concentration in IC50 equivalent of SSZ was calculated by dividing the IC50 of SSZ with DFMO combination from its corresponding single-agent IC50 value (IC50 of SSZ w/ DFMO comb/SSZ IC50). For DFMO, the concentration in IC50 equivalent was calculated by dividing its actual concentration used in the combination treatment from its corresponding single-agent IC50 value (DFMO/ DFMO IC50). Combination index (CI) at 50 % effect level is calculated by adding the IC50 equivalent concentration of SSZ and DFMO. CI >1.3 is antagonism; CI = 1.1-1.3 is moderate antagonism; CI = 0.9-1.1 is additive; CI = 0.8-0.9 is slight synergism; CI = 0.6-0.8 is moderate synergism; CI = 0.4-0.6 is synergism; CI = 0.2-0.4 is strong synergism. Synergism was detected at two different combinations of DFMO and SSZ in SK-N-Be(2)c cells and three different combinations in LAN-5 cells (bold italics). The data present the average of three independent experiments performed in duplicate (n = 6)