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. 2019 Jul 9;9:562. doi: 10.3389/fonc.2019.00562

Table 2.

Selectivity index of ruthenium complexes containing heterocyclic thioamidates.

Cancer cells Noncancerous cells
PBMCs MRC-5
(1) (2) (3) (4) DOX OXA (1) (2) (3) (4) DOX OXA
HepG2 1.0 1.4 1.8 1.6 8.3 4.3 0.9 0.8 0.7 N.d. 1.3 0.7
HL-60 1.4 2.4 2.6 2.6 12.5 15.7 1.2 1.5 1.1 N.d. 2.0 2.5
K-562 1.9 2.9 2.8 1.8 2.8 9.4 1.6 1.8 1.2 N.d. 0.4 1.5
B16-F10 1.5 2.0 3.3 1.3 12.5 4.3 1.3 1.2 1.4 N.d. 2.0 0.7
MCF-7 N.d. 0.4 1.5 N.d. 6.3 1.6 N.d. 0.2 0.6 N.d. 1.0 0.3
HCT116 N.d. 1.0 2.2 N.d. 8.3 2.3 N.d. 0.6 0.9 N.d. 1.3 0.4
HSC-3 N.d. 1.2 2.5 N.d. 5.0 2.9 N.d. 0.7 1.0 N.d. 0.8 0.5
SCC-4 N.d. 0.7 2.8 N.d. 0.6 1.2 N.d. 0.4 1.1 N.d. 0.1 0.2

The selectivity index (SI) of each complex was calculated using the following formula: SI = IC50 [noncancerous cells]/IC50 [cancer cells]. Cancer cells: HepG2 (human hepatocellular carcinoma); HL-60 (human acute promyelocytic leukemia); K-562 (human chronic myelogenous leukemia); B16-F10 (mouse melanoma); MCF-7 (human breast adenocarcinoma); HCT116 (human colon carcinoma); HSC-3 (human oral squamous cell carcinoma); and SCC-4 (human oral squamous cell carcinoma). Noncancerous cells: PBMCs (human peripheral blood mononuclear cells) and MRC-5 (human lung fibroblast). Doxorubicin (DOX) and oxaliplatin (OXA) were used as the positive controls. N.d. = Not determined.