Carvacrol enhances the sensitıvity of cetuximab in lung cancer cells through inducing apoptosis and cell cycle arrest

The intention of this work was to analyze that carvacrol could enhance cancer-inhibiting potency of cetuximab (monoclonal antibody) in lung cancer cells. The combination of cetuximab and carvacrol was found to co-operatively suppress cell proliferation by enhancing apoptosis and inducing cell cycle arrest in A-549 and H1299 cells. Furthermore, the combination therapy triggered cell death by inducing membrane disruption. The most effective combinations were IC₁₀ cetuximab + IC₁₀ carvacrol for A-549 and IC₂₀ cetuxi-mab + IC₁₀ carvacrol for H1299 (CI = 2.0). LDH activity increased by 101% in A-549 and 239% in H1299 (p<0.05). Caspase-3 activity rose by 1.6-fold in A-549 and 1.4-fold in H1299 (p<0.05). The combination decreased PCNA, topo-isomerase II-alpha, and cyclins D1, D2, E, A, and B (p<0.05). Overall, the com-bination of carvacrol and cetuximab appears to enhance anti-cancer efficacy and may significantly improve therapeutic outcomes in lung cancer cells.

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Publication Details

Journal
Bangladesh Journal of Pharmacology
Published
2025-04-25
DOI
https://doi.org/10.3329/bjp.v20i1.80949
Primary Topic
Synthesis and biological activity
Type
article
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article

Carvacrol enhances the sensitıvity of cetuximab in lung cancer cells through inducing apoptosis and cell cycle arrest

Ayşe Erdoğan, Rahime Aybike Koras
Bangladesh Journal of Pharmacology
Synthesis and biological activity
article

Carvacrol enhances the sensitıvity of cetuximab in lung cancer cells through inducing apoptosis and cell cycle arrest

Ayşe Erdoğan, Rahime Aybike Koras
article en

Abstract

The intention of this work was to analyze that carvacrol could enhance cancer-inhibiting potency of cetuximab (monoclonal antibody) in lung cancer cells. The combination of cetuximab and carvacrol was found to co-operatively suppress cell proliferation by enhancing apoptosis and inducing cell cycle arrest in A-549 and H1299 cells. Furthermore, the combination therapy triggered cell death by inducing membrane disruption. The most effective combinations were IC₁₀ cetuximab + IC₁₀ carvacrol for A-549 and IC₂₀ cetuxi-mab + IC₁₀ carvacrol for H1299 (CI = 2.0). LDH activity increased by 101% in A-549 and 239% in H1299 (p<0.05). Caspase-3 activity rose by 1.6-fold in A-549 and 1.4-fold in H1299 (p<0.05). The combination decreased PCNA, topo-isomerase II-alpha, and cyclins D1, D2, E, A, and B (p<0.05). Overall, the com-bination of carvacrol and cetuximab appears to enhance anti-cancer efficacy and may significantly improve therapeutic outcomes in lung cancer cells.

Bangladesh Journal of PharmacologyVol. 20(1)
Alanya University (TR), Alanya Alaaddin Keykubat Üniversitesi (TR)
Openalex Percentile: Top 91%
Synthesis and biological activity
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