Ursolic acid-enriched kudingcha extract enhances the antitumor activity of bacteria-mediated cancer immunotherapy

被引:0
|
作者
Xu, Haixia [1 ]
Piao, Linghua [2 ]
Liu, Xiande [1 ]
Jiang, Sheng-nan [3 ]
机构
[1] Hainan Univ, Sch Life Sci, 58 Renmin Ave, Haikou 570228, Hainan, Peoples R China
[2] Hainan Med Univ, Dept Physiol, Haikou, Hainan, Peoples R China
[3] Cent South Univ, Affiliated Haikou Hosp, Xiangya Sch Med, Dept Nucl Med, 43 Renmin Ave, Haikou 570208, Hainan, Peoples R China
关键词
BCI; Ursolic acid-enriched KDCE; Antiangiogenesis; VEGFR2; ANGIOGENESIS; APOPTOSIS; TSENG;
D O I
10.1186/s12906-022-03612-2
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background Bacteria-mediated cancer immunotherapy (BCI) robustly stimulates the immune system and represses angiogenesis, but tumor recurrence and metastasis commonly occur after BCI. The natural product Ilex kudingcha C. J Tseng enriched with ursolic acid has anti-cancer activity and could potentially augment the therapeutic effects of BCI. The objective of the present study was to determine potential additive effects of these modalities. Methods We investigated the anti-cancer activity of KDCE (Kudingcha extract) combined with S.toppGpp in the mice colon cancer models. Results In the present study, KDCE combined with S.toppGpp BCI improved antitumor therapeutic efficacy compared to S.toppGpp or KDCE alone. KDCE did not prolong bacterial tumor-colonizing time, but enhanced the antiangiogenic effect of S.toppGpp by downregulatingVEGFR2. We speculated that KDCE-induced VEGFR2 downregulation is associated with FAK/MMP9/STAT3 axis but not AKT or ERK. Conclusions Ursolic acid-enriched KDCE enhances the antitumor activity of BCI, which could be mediated by VEGFR2 downregulation and subsequent suppression of angiogenesis. Therefore, combination therapy with S.toppGpp and KDCE is a potential cancer therapeutic strategy.
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页数:9
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