TY - JOUR
T1 - Non-contact Electric Field Exposure Provides Potential Cancer Therapy through p53-Independent Proliferation Arrest and Intrinsic Pathway Apoptosis Induction in MG-63 Cell Lines
AU - Hasbullah, Omat Rachmat
AU - Fiddiyanti, Ilma
AU - Handayani, Dewi Ratih
AU - Sutedja, Endang
AU - Ismono, Darmadji
AU - Hidajat, Nucki Nursjamsi
AU - Widowati, Wahyu
AU - Afifah, Ervi
AU - Kusuma, Hanna Sari Widya
AU - Rizal, Rizal
AU - Alamsyah, Firman
AU - Taruno, Warsito P.
N1 - Funding Information:
We extend our gratitude to Agung Novianto, Viranda andria Yuninda, Anis Syahbani Muthmainnah and Afif Yati from Aretha Medika Utama, Biomolecular and Biomedical Research Center, Bandung, West Java, Indonesia for their technical support.
Publisher Copyright:
© 2023, Bogor Agricultural University. All rights reserved.
PY - 2023/5
Y1 - 2023/5
N2 - Osteosarcoma is a highly malignant primary tumor on bone that mainly attacks children and young adolescents. Until now, osteosarcoma therapy still combines some high costs and invasive therapy modalities that may give side effects, such as pain and nausea. Our previous studies suggested that non-contact electric field has anti-proliferative effect on breast cancer cells, in vitro and in vivo. In this study, we were interested studying alternating current electric field effects on osteosarcoma cells progression as well as its potential cytotoxic effects. MG-63 human osteosarcoma cells were cultured and treated with 200 kHz for 6 days. Several genes of interest including p53, p21, MDM2, caspase-3, caspase-8, and caspase-9 were analyzed using real-time qPCR method. Apoptotic index was measured using flow-cytometry assay. Apoptosis was observed through p53-independent p21 pathway (p = 0.011). Cells undergoing apoptosis through internal pathways were shown by the increase of caspase-3 (p = 0.015) and caspase-9 (p = 0.001) levels, but not caspase-8 (p = 0.080). This treatment has successfully reduced the number of living osteosarcoma cells by 14.7% (p = 0.000) and increased cell death up to 4.26% (p = 0.055). Apoptotic index was markedly increased to 16% (p = 0.001). 200 kHz non-contact electric field exposure can disrupt osteosarcoma progression through disruption of normal cell cycle via p53-independent p21 pathway and induction of apoptosis.
AB - Osteosarcoma is a highly malignant primary tumor on bone that mainly attacks children and young adolescents. Until now, osteosarcoma therapy still combines some high costs and invasive therapy modalities that may give side effects, such as pain and nausea. Our previous studies suggested that non-contact electric field has anti-proliferative effect on breast cancer cells, in vitro and in vivo. In this study, we were interested studying alternating current electric field effects on osteosarcoma cells progression as well as its potential cytotoxic effects. MG-63 human osteosarcoma cells were cultured and treated with 200 kHz for 6 days. Several genes of interest including p53, p21, MDM2, caspase-3, caspase-8, and caspase-9 were analyzed using real-time qPCR method. Apoptotic index was measured using flow-cytometry assay. Apoptosis was observed through p53-independent p21 pathway (p = 0.011). Cells undergoing apoptosis through internal pathways were shown by the increase of caspase-3 (p = 0.015) and caspase-9 (p = 0.001) levels, but not caspase-8 (p = 0.080). This treatment has successfully reduced the number of living osteosarcoma cells by 14.7% (p = 0.000) and increased cell death up to 4.26% (p = 0.055). Apoptotic index was markedly increased to 16% (p = 0.001). 200 kHz non-contact electric field exposure can disrupt osteosarcoma progression through disruption of normal cell cycle via p53-independent p21 pathway and induction of apoptosis.
KW - Cancer
KW - Caspase 8
KW - Caspase 9
KW - MDM2
KW - p21
KW - p53
UR - http://www.scopus.com/inward/record.url?scp=85150164436&partnerID=8YFLogxK
U2 - 10.4308/hjb.30.3.522-531
DO - 10.4308/hjb.30.3.522-531
M3 - Article
AN - SCOPUS:85150164436
SN - 1978-3019
VL - 30
SP - 522
EP - 531
JO - HAYATI Journal of Biosciences
JF - HAYATI Journal of Biosciences
IS - 3
ER -