Sodium chloride (NaCl) potentiates digoxin-induced anti-tumor activity in small cell lung cancer

Cancer Biol Ther. 2019;20(1):52-64. doi: 10.1080/15384047.2018.1504723. Epub 2018 Sep 5.

Abstract

Small cell lung cancer (SCLC) is a malignant neuroendocrine tumor with very high mortality. Effective new therapy for advanced SCLC patients is urgently needed. By screening a FDA-approved drug library, we identified a cardiac glycoside (CG), namely digoxin (an inhibitor of cellular Na+/K+ ATPase pump), which was highly effective in inhibiting SCLC cell growth. Intriguing findings showed that NaCl supplement markedly enhanced the anti-tumor activities of digoxin in both in vitro and in vivo models of SCLC. Subsequent analysis revealed that this novel combination of digoxin/NaCl caused an up-regulation of intracellular Na+ and Ca2+ levels with an induction of higher resting membrane potential of SCLC cells. We also found that this combination lead to morphological shrinking of SCLC cells, together with high levels of cytochrome C release. Lastly, our data revealed that NaCl supplement was able to induce the expression of ATP1A1 (a Na+/K+ ATPase subunit), in which contributes directly to the increased sensitivity of SCLC cells to digoxin. Thus, this is the first demonstration that NaCl is a potent supplement necessitating superior anti-cancer effects of digoxin for SCLC. Further, our study suggests that digoxin treatment could need to be combined with NaCl supplement in future clinical trial of SCLC, particularly where low Na+ is often present in SCLC patients.

Keywords: ATP1A1; NaCl; cardiac glycosides; digoxin; small cell lung cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / pharmacology*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Cell Line, Tumor
  • Digoxin / pharmacology*
  • Digoxin / therapeutic use
  • Drug Screening Assays, Antitumor
  • Drug Synergism
  • High-Throughput Screening Assays
  • Humans
  • Lung Neoplasms / blood
  • Lung Neoplasms / drug therapy*
  • Lung Neoplasms / pathology
  • Membrane Potentials / drug effects
  • Small Cell Lung Carcinoma / blood
  • Small Cell Lung Carcinoma / drug therapy*
  • Small Cell Lung Carcinoma / pathology
  • Sodium / blood
  • Sodium Chloride / pharmacology*
  • Sodium Chloride / therapeutic use
  • Sodium-Potassium-Exchanging ATPase / antagonists & inhibitors

Substances

  • Sodium Chloride
  • Digoxin
  • Sodium
  • ATP1A1 protein, human
  • Sodium-Potassium-Exchanging ATPase

Grants and funding

This work was supported by National Natural Science Foundation of China [81502632]; National Natural Science Foundation of China [81372214]; Natural Science Foundation of Anhui Province [1608085MH179]; Key Technologies R & D Program of Anhui Province [1604a0802103]; The Major/Innovative Program of Development Foundation of Hefei Center for Physical Science and Technology [2016FXCX006]; National Natural Science Foundation of China [31601134]; National Natural Science Foundation of China [61727811], Innovative program (ZT00102901), Natural Science Foundation of Anhui Province [1708085QC57]; Research Grant Council, Hong Kong [17114814]; Research Grant Council, Hong Kong [17121616]; Research Grant Council, Hong Kong [T12-401/13-R].