Paeoniflorin Induces Apoptosis in NSCLC Cells via Activating Hippo Signaling Pathway
10.13422/j.cnki.syfjx.20232023
- VernacularTitle:芍药苷干预Hippo信号通路诱导非小细胞肺癌凋亡的机制
- Author:
Yan LI
1
;
Liang PENG
2
;
Lifeng JIANG
1
;
Sheng WANG
1
;
Ge WANG
1
;
Xiaolin YU
1
;
Yulin YAO
3
Author Information
1. The Affiliated Cancer Hospital of Zhengzhou University/Henan Cancer Hospital， Zhengzhou 450008， China
2. Fuwai Central China Cardiovascular Hospital/Henan Provincial People's Hospital， Zhengzhou 451464， China
3. Henan University of Chinese Medicine， Zhengzhou 450046， China
- Publication Type:Journal Article
- Keywords:
paeoniflorin;
Hippo pathway;
anoxia;
apoptosis
- From:
Chinese Journal of Experimental Traditional Medical Formulae
2024;30(12):39-44
- CountryChina
- Language:Chinese
-
Abstract:
ObjectiveTo observe the apoptosis induced by paeoniflorin （PF） in non-small cell lung cancer （NSCLC） cells and explore its mechanism. MethodCell counting kit-8 （CCK-8） was used to detect the inhibition rates of H1299， H292 and A549 cells with different concentrations of PF （2.5， 5， 10， 20， 25 µmol·L-1）， and to screen suitable concentrations of PF and experimental cells. The inhibitory effect of PF on lung cancer cells was detected by clone formation assay. The effect of PF on cell apoptosis was detected by flow cytometry with annexin V-FITC/propidium iodide （PI） double staining. With the right concentration of drugs， levels of apoptosis-associated protein B-cell lymphoma-2 （Bcl-2）， Bcl-2-associated X protein （Bax）， cleaved Caspase-3 and Caspase-3 were detected by Western blot. At the same time， the molecular expressions of hypoxia inducible factor -1α （HIF-1α） and Hippo signaling pathway were determined. ResultCompared with the blank group， PF significantly inhibited the growth of H1299， H292 and A549 cells of human lung cancer （P<0.01）. PF significantly induced apoptosis in A549 cells （P<0.01）， decreased the Bcl-2/Bax ratio （P<0.01）， and significantly increased the cleaved Caspase-3 expression （P<0.01）. Compared with those in the blank group， the expression levels of HIF-1α， transcriptional coactivator with PDZ-binding motif （TAZ）， large tumor suppressor 1 （LATS1）， Mps one binding 1 （MOB1） and Yes-associated protein （YAP） in A549 cells of the PF treatment group were significantly decreased （P<0.01）， while the expressions of p-LATS1， p-MOB1 and p-YAP were significantly increased （P<0.01）. At the same time， there was no significant effect on the expression levels of phosphorylated mammalian Ste20-like kinase 1 （p-MST1） and MST1， which did not reach a statistical difference. ConclusionAll data demonstrated that PF showed an anti-tumor effect by improving hypoxic conditions and inhibiting the abnormally activated Hippo signaling pathway， thereby inducing and promoting apoptosis in non-small cell lung cancer.
