TY - JOUR
T1 - Stem bark ethanolic extract of Pinus merkusii induces caspase 9-mediated apoptosis in HeLa cells
AU - Achmad, Agung Budianto
AU - Proboningrat, Annise
AU - Ansori, Arif Nur Muhammad
AU - Fadholly, Amaq
AU - Rochmi, Siti Eliana
AU - Samsudin, Rinza Rahmawati
AU - Hidayatik, Nanik
AU - Hendarti, Gracia Angelina
AU - Jayanti, Shara
N1 - Publisher Copyright:
© 2024, Faculty of Veterinary Medicine, University of Tripoli. All rights reserved.
PY - 2024
Y1 - 2024
N2 - Background: Cervical cancer is a severe concern for women throughout the world. This percentage of cancer incidence causes sufferers to die at a high rate. It is believed that the bark of the Pinus merkusii tree contains anti-cancer compounds that inhibit cervical cancer cell growth. Aim: This present study aims to examine the cytotoxic ability of P. merkusii tree bark ethanol extract (PMBE) by inducing apoptosis in HeLa cells. Methods: We administered the PMBE at concentrations of 50, 100, 200, and 400 µg/ml to HeLa cell cultures. We then conducted the MTT cytotoxicity assay, detected apoptosis via Annexin V binding, and observed caspase 9 expression via immunocytochemistry. Results: PMBE showed cytotoxic activity on HeLa cells with an IC50 of 226.6 µg/ml for 24 hours of treatment. PMBE caused early apoptosis in up to 81.31% of HeLa cells, as well as increased caspase-9 expression. Conclusion: Based on this study, PMBE is predicted to have dose-dependent antiproliferative or cytotoxicity effects on the HeLa cell line through the intrinsic pathway apoptosis mechanism.
AB - Background: Cervical cancer is a severe concern for women throughout the world. This percentage of cancer incidence causes sufferers to die at a high rate. It is believed that the bark of the Pinus merkusii tree contains anti-cancer compounds that inhibit cervical cancer cell growth. Aim: This present study aims to examine the cytotoxic ability of P. merkusii tree bark ethanol extract (PMBE) by inducing apoptosis in HeLa cells. Methods: We administered the PMBE at concentrations of 50, 100, 200, and 400 µg/ml to HeLa cell cultures. We then conducted the MTT cytotoxicity assay, detected apoptosis via Annexin V binding, and observed caspase 9 expression via immunocytochemistry. Results: PMBE showed cytotoxic activity on HeLa cells with an IC50 of 226.6 µg/ml for 24 hours of treatment. PMBE caused early apoptosis in up to 81.31% of HeLa cells, as well as increased caspase-9 expression. Conclusion: Based on this study, PMBE is predicted to have dose-dependent antiproliferative or cytotoxicity effects on the HeLa cell line through the intrinsic pathway apoptosis mechanism.
KW - Anticancer
KW - Apoptosis
KW - Cervical cancer
KW - Pinaceae
UR - http://www.scopus.com/inward/record.url?scp=85208695705&partnerID=8YFLogxK
U2 - 10.5455/OVJ.2024.v14.i10.12
DO - 10.5455/OVJ.2024.v14.i10.12
M3 - Article
AN - SCOPUS:85208695705
SN - 2226-4485
VL - 14
SP - 2628
EP - 2633
JO - Open Veterinary Journal
JF - Open Veterinary Journal
IS - 10
ER -