TY - JOUR
T1 - Antitumor activity of Pinoresinol in vitro
T2 - Inducing apoptosis and inhibiting HepG2 invasion
AU - Zhang, Yawen
AU - Zhao, Haobin
AU - Di, Yichao
AU - Li, Qi
AU - Shao, Dongyan
AU - Shi, Junling
AU - Huang, Qingsheng
N1 - Publisher Copyright:
© 2018
PY - 2018/6
Y1 - 2018/6
N2 - (+)-Pinoresinol (Pin), a biologically active lignan and widely found in many dietary plants, was reported to have antifungal, anti-inflammatory, antioxidation, and hypoglycemic activities. In the present study, the capability of Pin to inhibit human hepatocellular carcinoma HepG2 cells was evaluated and the mechanism was analyzed. Pin exhibited significant inhibition of HepG2 proliferation and revealed a pro-apoptotic effect. Pin led to activation of Fas, FasL, caspase-8, and Bid, which provoked death receptor apoptotic signals. Significant loss of mitochondrial membrane potential was also observed, as well as the altered expression of mitochondrial apoptotic proteins, including increased Cyto-c, Bax/Bcl-2 ratio, and caspase 3. Pin also exhibited inhibitory effect on the migration and invasion of HepG2 in a concentration-dependent manner by increasing E-cadherin and decreasing VCAM-1, ICAM-1 and MMP-9 expression. All the results indicated Pin could inhibit HepG2 via the induction of apoptosis through the death receptor pathway and/or mitochondrial pathway and the inhibition of invasion via disturbing the cytoskeleton.
AB - (+)-Pinoresinol (Pin), a biologically active lignan and widely found in many dietary plants, was reported to have antifungal, anti-inflammatory, antioxidation, and hypoglycemic activities. In the present study, the capability of Pin to inhibit human hepatocellular carcinoma HepG2 cells was evaluated and the mechanism was analyzed. Pin exhibited significant inhibition of HepG2 proliferation and revealed a pro-apoptotic effect. Pin led to activation of Fas, FasL, caspase-8, and Bid, which provoked death receptor apoptotic signals. Significant loss of mitochondrial membrane potential was also observed, as well as the altered expression of mitochondrial apoptotic proteins, including increased Cyto-c, Bax/Bcl-2 ratio, and caspase 3. Pin also exhibited inhibitory effect on the migration and invasion of HepG2 in a concentration-dependent manner by increasing E-cadherin and decreasing VCAM-1, ICAM-1 and MMP-9 expression. All the results indicated Pin could inhibit HepG2 via the induction of apoptosis through the death receptor pathway and/or mitochondrial pathway and the inhibition of invasion via disturbing the cytoskeleton.
KW - Antitumor activity
KW - Apoptosis
KW - Cell migration
KW - HepG2
KW - Pinoresinol
UR - http://www.scopus.com/inward/record.url?scp=85045266022&partnerID=8YFLogxK
U2 - 10.1016/j.jff.2018.04.009
DO - 10.1016/j.jff.2018.04.009
M3 - 文章
AN - SCOPUS:85045266022
SN - 1756-4646
VL - 45
SP - 206
EP - 214
JO - Journal of Functional Foods
JF - Journal of Functional Foods
ER -