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. 2019 Jul 16;10(44):4570–4586. doi: 10.18632/oncotarget.27068

Table 1. The lowest significant dose (LSDs) and IC50 doses of cisplatin (CSP), cyclophosphamide (CYCLO) and chlorambucil (CLB) which reduced ATP levels and increased caspase 3 activity (CASP 3) when compared to the vehicle control (P ≤ 0.05) in two lymphoid (Jurkat and CCRF-CEM) and two myeloid (THP1 and KG-1a) leukaemia cell lines; and two non-tumour control hematopoietic stem cells (CD34+ HSCs and CD133+ HSCs).

Cell type Doses CSP CYCLO CLB
ATP CASP 3 ATP CASP 3 ATP CASP 3
Lymphoid Cells Jurkat LSD 0.01 μM 0.01 μM 2 μM 10 μM 10 μM 10 μM
IC50 0.4 μM 4.5 μM >50 μM 50 μM >50 μM >50 μM
CCRF-CEM LSD 2 μM 0.4 μM 10 μM 10 μM 0.01 μM 10 μM
IC50 15 μM 6 μM >50 μM >50 μM 6.5 μM >50 μM
Myeloid Cells THP1 LSD 0.01 μM 0.01 μM 0.4 μM 2 μM 0.4 μM 0.4 μM
IC50 5.5 μM 5 μM >50 μM >50 μM >50 μM >50 μM
KG1a LSD 2 μM 2 μM 50 μM 50 μM 10 μM 10 μM
IC50 >50 μM >50 μM >50 μM >50 μM >50 μM >50 μM
Non-Tumor Control Cells CD34+ HSCs LSD 0.4 μM 0.4 μM 2 μM 2 μM 2 μM 10 μM
IC50 10 μM >50 μM >50 μM >50 μM 40 μM >50 μM
CD133+ HSCs LSD 0.4 μM 2 μM 10 μM 10 μM 10 μM 10 μM
IC50 40 μM 30 μM >50 μM >50 μM >50 μM >50 μM

The LSDs for ATP levels where used in subsequent investigation of combination treatments on cell-cycle progression, ATP and glutathione levels and DNA damage. The LSDs for caspase 3 activity were used for further investigation of apoptosis.