Anti-cancer potentials of Gynura procumbens leaves extract against two canine mammary cancer cell lines

被引:3
|
作者
Jermnak, Usuma [1 ]
Supsavhad, Wachiraphan [2 ]
Kunakornsawat, Sunee [3 ]
Jaroensong, Tassanee [3 ]
Watcharasit, Piyajit [4 ]
Visitnonthachai, Daranee [4 ]
Pairor, Selapoom [3 ]
Phaochoosak, Napasorn [1 ]
机构
[1] Kasetsart Univ, Fac Vet Med, Dept Pharmacol, Bangkok 10900, Thailand
[2] Kasetsart Univ, Fac Vet Med, Dept Pathol, Bangkok, Thailand
[3] Kasetsart Univ, Fac Vet Med, Dept Compan Anim Clin Sci, Bangkok, Thailand
[4] Chulabhorn Res Inst, Lab Pharmacol, Bangkok, Thailand
关键词
anti-cancer properties; canine mammary cancer; EGFR signalling pathway; Gynura procumbens; leaves extract; TUMOR-SUPPRESSOR GENE; GLAND TUMORS; PTEN; EXPRESSION; APOPTOSIS; PROLIFERATION; EPIDEMIOLOGY; METASTASIS; CARCINOMAS; TOXICITY;
D O I
10.1002/vms3.684
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Background: The anti-cancer effects of Gynura procumbens leaves extract (GPE) have been reported in various human cancers. However, the anti-cancer effects and molecular mechanisms of this extract on canine mammary cancer (CMC) have not yet been elucidated. Objectives: The main goal of this study was to investigate the anti-cancer properties of GPE against two CMC cell lines (CHMp-13a and CHMp-5b). Methods: The GP leaves were extracted with 80% ethanol. Anti-cancer potentials of GPE on CHM p-13a and CHM p-5b cancer cell lines using dimethyl-2-thiazolyl-2,5-diphenyl-2H-tetrazolium bromide (MTT), wound healing, transwell migration, and caspase 3/7 activity assays were evaluated. The mRNA expression levels of two oncogenes: epidermal growth factor receptor (EGFR) and twist family bHLH transcription factor 1 (TWIST) and one tumour suppressor gene: phosphatase and tensin homolog (PTEN) in these cell lines were determined by quantitative real-time PCR (qRT-PCR). In addition, The EGFR and PTEN protein levels as well as protein kinase B (AKT) and extracellular signal-regulated kinase 1/2 (ERK1/2) phosphorylation levels expression were also evaluated by western blot analysis. Results: The results showed that GPE caused a significant concentration- and time-dependent reduction in cell proliferation of both CHMp-13a and CHM p-5b cells, detected by MTT assays. This extract also significantly suppressed cancer cell migration in both cell lines, tested by wound healing and transwell migration assays. Additionally, the increase in caspase 3/7 activity observed in both CMC cell treated with GPE suggests that GPE induced caspase 3/7 dependent apoptosis. Moreover, GPE significantly decreased EGFR m RNA and protein expression levels corn pared to control in both cell lines in a dose-dependent manner. Conclusion: These findings emphasized that GPE has an in vitro anti-cancer activity against CMC by inhibiting EGFR signalling pathway. Thus, GPE may serve as an alternative therapy in CMC with high EGFR expression.
引用
收藏
页码:69 / 84
页数:16
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