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消癌平注射液通过 pregnane X 受体及其下游分子增强紫杉醇在卵巢癌中的疗效。

Xiaoaiping injection enhances paclitaxel efficacy in ovarian cancer via pregnane X receptor and its downstream molecules.

机构信息

Department of Pharmacy, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, 600 Yi Shan Road, Shanghai, 200233, China.

College of Food Science and Technology, Shanghai Ocean University, 999 Huan Hucheng Road, Shanghai, 201306, China.

出版信息

J Ethnopharmacol. 2020 Oct 28;261:113067. doi: 10.1016/j.jep.2020.113067. Epub 2020 Jun 4.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Xiaoaiping injection, a traditional Chinese medical injection extracted from root of Marsdenia tenacissima (Roxb.) Moon, has been exclusively used on curing malignant tumor in China and as adjuvant therapeutic agent for chemotherapeutics, including paclitaxel.

AIM OF THE STUDY

The goal of this study was to investigate the synergistic inhibitory efficacy of Xiaoaiping injection and paclitaxel on ovarian cancer. The mechanism may be associated with nuclear receptor pregnane X receptor (PXR) regulating its downstream molecules.

MATERIALS AND METHODS

In vitro, MTT assay, flow cytometry and Hoechst dyeing were used to evaluate the SK-OV-3 cell proliferation, apoptosis and cell cycle respectively. The mRNA and protein expression of PXR and its downstream CYP450 enzymes, transporters and Bcl-2 families were measured by qRT-PCR and Western blot. Rhodamine 123 efflux experiment was conducted to detect the P-gp efflux ability. PXR plasmid and PXR siRNA were transiently transfected into SK-OV-3 cells respectively to establish PXR-overexpressed or PXR-interfered cells. In vivo, xenograft tumor mice model was established by SK-OV-3 cells to estimate the antitumor effect of Xiaoaiping injection combined with paclitaxel. The expressions of PXR and its downstream molecules in tumor tissues were determined to further clarify the potential mechanism.

RESULTS

Xiaoaiping injection significantly enhanced the anti-proliferation, pro-apoptosis effect of paclitaxel on SK-OV-3 cells. The synergetic effect was displayed by Xiaoaiping injection inhibiting paclitaxel-induced PXR and CAR expression, which subsequently inhibited CYP450 enzymes CYP2C8 and CYP3A4, transporter P-gp and anti-apoptotic proteins Bcl-2 and Bcl-xl in SK-OV-3 cells. In PXR-overexpressed cells, Xiaoaiping injection down-regulated the expression of PXR and its downstream molecules. The result of xenograft tumor model showed that Xiaoaiping injection combined with paclitaxel enhanced anti-tumor effect on ovarian cancer in vivo.

CONCLUSIONS

Xiaoaiping injection enhances anti-tumor effect of paclitaxel by inhibiting cell proliferation, inducing apoptosis process. The mechanism may be associated with Xiaoaiping injection inhibiting PXR and its downstream metabolic enzymes CYP2C8, CYP3A4, transporter P-gp and anti-apoptosis protein Bcl-2.

摘要

民族药理学相关性

消癌平注射液是从中国马兜铃科植物天仙藤中提取的中药注射液,在中国仅用于治疗恶性肿瘤,并作为紫杉醇等化疗药物的辅助治疗药物。

研究目的

本研究旨在探讨消癌平注射液与紫杉醇联合应用对卵巢癌的协同抑制作用。其机制可能与核受体孕烷 X 受体(PXR)调节其下游分子有关。

材料与方法

体外实验采用 MTT 法、流式细胞术和 Hoechst 染色分别评价 SK-OV-3 细胞增殖、凋亡和细胞周期。采用 qRT-PCR 和 Western blot 检测 PXR 及其下游 CYP450 酶、转运体和 Bcl-2 家族的 mRNA 和蛋白表达。采用罗丹明 123 外排实验检测 P-gp 外排能力。分别用 PXR 质粒和 PXR siRNA 瞬时转染 SK-OV-3 细胞,建立 PXR 过表达或 PXR 干扰细胞。体内实验采用 SK-OV-3 细胞建立异种移植肿瘤小鼠模型,评价消癌平注射液联合紫杉醇的抗肿瘤作用。进一步阐明潜在机制,检测肿瘤组织中 PXR 及其下游分子的表达。

结果

消癌平注射液显著增强了紫杉醇对 SK-OV-3 细胞的抗增殖、促凋亡作用。消癌平注射液抑制紫杉醇诱导的 PXR 和 CAR 表达,进而抑制 CYP450 酶 CYP2C8 和 CYP3A4、转运体 P-gp 和抗凋亡蛋白 Bcl-2 和 Bcl-xl 在 SK-OV-3 细胞中的表达,显示出协同作用。在 PXR 过表达细胞中,消癌平注射液下调了 PXR 及其下游分子的表达。异种移植肿瘤模型的结果表明,消癌平注射液联合紫杉醇增强了对卵巢癌的体内抗肿瘤作用。

结论

消癌平注射液通过抑制细胞增殖、诱导凋亡过程增强紫杉醇的抗肿瘤作用。其机制可能与消癌平注射液抑制 PXR 及其下游代谢酶 CYP2C8、CYP3A4、转运体 P-gp 和抗凋亡蛋白 Bcl-2 有关。

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