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Effects of curcumin on proliferation, migration, invasion and apoptosis of endometrial carcinoma HEC-1-B cells through p53/AMPK signaling pathway
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DOI   10.11656/j.issn.1673-9043.2025.09.06
Key Words   curcumin;AMPK;compound C;endometrial cancer
Author NameAffiliationE-mail
WEN Mengke Uterine Corpus Tumor Ward of Gynecological Center, Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi 830001, China  
ZHAO Shihong Uterine Corpus Tumor Ward of Gynecological Center, Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi 830001, China  
SHEN Guqun Uterine Corpus Tumor Ward of Gynecological Center, Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi 830001, China 382709897@qq.com 
Abstract
    Objective Exploring the biological effects of curcumin on human endometrial cancer cell line HEC-1-B by affecting the AMPK signaling pathway. Methods Firstly, HEC-1-B cells were treated with different concentrations of curcumin(0, 5, 10, 20, 40 μmol/L), and the inhibition rate of cell proliferation was detected by MTT assay. Divided HEC-1-B cells into control group(untreated) and compound C group(10 μmol/L), Curcumin group(20 μmol/L) and curcumin(20 μ mol/L)+compound C(10 μmol/L group), the drug action time was 48 hours. The proliferation of HEC-1-B cells was detected by MTT method, and the migration and invasion of HEC-1-B cells were detected by scratch assay and transwell, respectively. The apoptosis of HEC-1-B cells was detected by flow cytometry. The expression levels of caspase 3, Bcl-2, Bax mRNA in HEC-1-B cells were detected by RT-PCR, and the expression of caspase 3, Bcl-2, Bax, and AMPK signaling pathway proteins in HEC-1-B cells were detected by Western blot. Results Compared with 0 μmol/L, the proliferation inhibition rate of 5 μmol/L curcumin was not significant(P>0.05). The proliferation inhibition rates of 10 μmol/L, 20 μmol/L, and 40 μmol/L curcumin were significantly increased(P < 0.05) and showed a dose-dependent effect; Compared with the control group, the curcumin group showed a significant decrease in cell proliferation, migration, and invasion(P < 0.05), a significant increase in apoptosis(P < 0.05), an increase in caspase 3 and Bax expression(P < 0.05), and a decrease in Bcl-2 expression(P < 0.05);The expression of p-AMPK and p-p53 proteins increased(P < 0.05);In the compound C group, cell proliferation, migration, and invasion were significantly increased(P < 0.05), apoptosis was significantly reduced(P < 0.05), caspase 3 and Bax expression were reduced(P < 0.05), and Bcl-2 expression was increased(P < 0.05);The expression of p-AMPK and p-p53 proteins decreased(P < 0.05);There was no significant change in various indicators of cells in the curcumin+compound C group(P>0.05). Conclusion Curcumin affects the proliferation, migration, invasion, and apoptosis of endometrial cancer HEC-1-B cells by interfering with the p53/AMPK signaling pathway.

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