scorpion venom induces G2/M cell cycle arrest and apoptotic cell death in human non-small lung cancer cell lines.

BACKGROUND

Non-small cell lung cancers (NSCLC) represent the primary cause of cancer-related deaths worldwide. venom has been shown to exert cytotoxic effects against a panel of epithelial cancer cells and suggested that NSCLC was the subtype most susceptible to the treatment.

METHODS

This study evaluated the effect of scorpion venom on cell viability, in non-cancerous (MRC-5, lung; CHO-K1, ovary) and NSCLC (A549; NCI-H460) cell lines. The effects on cell cycle, apoptosis, and cell signaling-related proteins were determined by flow cytometry and WB. Protein fractions responsible for the observed effect were identified using HPLC.

RESULTS

Scorpion venom was more effective against NSCLC than non-cancerous cells. E values were 20.0 ± 5.8% and 22.47 ± 6.02% in A549 and NCI-H460 cancer cells, respectively, as compared to 50 ± 8.1% in MRC-5 and 54.99 ± 7.39% in CHO-K1 cells. It arrested NSCLC cells in the G2/M phase, while non-cancerous cells were arrested in the S (MRC-5) or G0/G1 (CHO-K1) phases. No changes were observed in the Bax/Bcl-2 or the cleaved-caspase 3/Total caspase 3 ratios in cells treated with venom. Likewise, the scorpion venom treatment did not affect p-ERK, p-AKT, or p-38MAPK protein levels. In contrast, scorpion venom treatment increased the cytosolic apoptosis-inducing factor (AIF) in A549 cells, indicating caspase-independent apoptosis. Additionally, combined etoposide/venom exposure provoked G2/M arrest and apoptosis in NSCLC more strongly than either substance alone. Furthermore, upon crude venom fractioning through RP-HPLC, we found two soluble fractions with high cytotoxic effects.

CONCLUSION

The present study concludes that a specific fraction of venom reduces cell viability of NSCLC cells. The AIF protein plays a key role in mediating caspase-independent apoptotic cell death. These findings suggest that venom enhances the anticancer effect of etoposide by causing cell cycle arrest and caspase-independent apoptosis.