TY - JOUR
T1 - Therapeutic potential of α,β-thujone through metabolic reprogramming and caspase-dependent apoptosis in ovarian cancer cells
AU - Lee, Jin Young
AU - Park, Hahyun
AU - Lim, Whasun
AU - Song, Gwonhwa
N1 - Funding Information:
This study was supported by the National Research Foundation of Korea (NRF) grant, funded by the Ministry of Science and ICT(MSIT), Republic of Korea; Contract grant number: 2018R1C1B6009048
Funding Information:
This study was supported by the National Research Foundation of Korea (NRF) grant, funded by the Ministry of Science and ICT(MSIT), Republic of Korea; Contract grant number: 2018R1C1B6009048 The authors declare that there are no conflict of interests.
Publisher Copyright:
© 2020 Wiley Periodicals LLC
PY - 2021/2
Y1 - 2021/2
N2 - The therapeutic potential of α,β-thujone, a functional compound found in many medicinal plants of the Cupressaceae, Asteraceae, and Lamiaceae families, has been demonstrated, including in inflammation and cancers. However, its pharmacological functions and mechanisms of action in ovarian cancer remain unclear. We investigated the anticancer properties of α,β-thujone in ES2 and OV90 human ovarian cancer cells and its effect on sensitization to cisplatin. α,β-thujone inhibited cancer cell proliferation and induced cell death through caspase-dependent intrinsic apoptotic pathways. Moreover, α,β-thujone-mediated endoplasmic reticulum stress was associated with the loss of mitochondrial functions and altered metabolic landscape of ovarian cancer cells. α,β-Thujone attenuated blood vessel formation in transgenic zebrafish, implying it has significant antiangiogenic potential. In addition, α,β-thujone sensitized ovarian cancer cells to cisplatin, causing synergistic pharmacological effects. Collectively, our results suggest that α,β-thujone has therapeutic potential in human ovarian cancer and functions via regulating multiple intracellular stress-associated metabolic reprogramming and caspase-dependent apoptotic pathways.
AB - The therapeutic potential of α,β-thujone, a functional compound found in many medicinal plants of the Cupressaceae, Asteraceae, and Lamiaceae families, has been demonstrated, including in inflammation and cancers. However, its pharmacological functions and mechanisms of action in ovarian cancer remain unclear. We investigated the anticancer properties of α,β-thujone in ES2 and OV90 human ovarian cancer cells and its effect on sensitization to cisplatin. α,β-thujone inhibited cancer cell proliferation and induced cell death through caspase-dependent intrinsic apoptotic pathways. Moreover, α,β-thujone-mediated endoplasmic reticulum stress was associated with the loss of mitochondrial functions and altered metabolic landscape of ovarian cancer cells. α,β-Thujone attenuated blood vessel formation in transgenic zebrafish, implying it has significant antiangiogenic potential. In addition, α,β-thujone sensitized ovarian cancer cells to cisplatin, causing synergistic pharmacological effects. Collectively, our results suggest that α,β-thujone has therapeutic potential in human ovarian cancer and functions via regulating multiple intracellular stress-associated metabolic reprogramming and caspase-dependent apoptotic pathways.
KW - apoptosis
KW - metabolic reprogramming
KW - ovarian cancer
KW - zebrafish
KW - α
KW - β-thujone
UR - http://www.scopus.com/inward/record.url?scp=85091731228&partnerID=8YFLogxK
U2 - 10.1002/jcp.30086
DO - 10.1002/jcp.30086
M3 - Article
C2 - 33000501
AN - SCOPUS:85091731228
SN - 0021-9541
VL - 236
SP - 1545
EP - 1558
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
IS - 2
ER -