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. 2018 Aug;366(2):303–313. doi: 10.1124/jpet.118.249359

TABLE 5.

In vitro effects of nicotine in combination with chemotherapy on lung cancer under nonphysiologic conditions and/or with nonpharmacological concentrations of nicotine

Lung Cancer Cell Line Nicotine Chemotherapy Duration of Treatment Serum Concentration Cellular Response (Assay) Result (Relative to Chemotherapy Alone) Reference
A549 1 μM Cisplatin 20 μM 24 h 0% for 36 h, then treated Apoptosis (TUNEL) 40% decrease* Dasgupta et al. (2011)
H446 2.5–15 μM Cisplatin 10 μM 12–72 h 10% Viability (MTT) 10%–20% increase (2.5 μM), Zeng et al. (2012)
0%–50% decrease (5–15 μM)
36 h Apoptosis (AV/PI) 25%–50% decrease*
A549, H1299, H23 1 μM Cisplatin 20 μM 36 h 0% Apoptosis (TUNEL) 20%–40% decrease Dasgupta et al. (2006)
Gemcitabine 20 μM 20%–25% decrease
Paclitaxel 20 μM 25%–50% decrease
N417 Previous nicotine exposure (500 μM for 7 days) Cisplatin (5–100 μM) 48 h 10% Viability (MTT) 50% increase* Martínez-García et al. (2010)
Etoposide (5–100 μM) 50% increase*
Mitomycin (5–50 μM) IC50 10 μM → 20 μM*
Paclitaxel (5–100 μM) IC50 35 μM → 70 μM*
201T 10 μM Gefitinib 35 μM 48 h 10% Viability (MTS) 47% increase (10 μM)* Carlisle et al. (2007)
A549 1 μM Gemcitabine 10 μM 36 h 0% for 24 h, then treated Apoptosis (TUNEL) 20% decrease* Guo et al. (2013)
H157, H1703 10 μM Paclitaxel 100 nM 48 h 0.1% Apoptosis (sub-G1) 8% decrease* Tsurutani et al. (2005)
Etoposide 100 μM 15% decrease*

AV/PI, annexin V/propidium iodide; MTS, (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium); MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; TUNEL, terminal deoxynucleotidyl transferase dUTP nick-end labeling.

*

Statistically significant.

Statistical significance not indicated.