Evidence map›Paper›PMID 35117420›Full record

ArticleTranslational cancer research2020

Effect of curcumin-lipiodol emulsion combined with absorbable anti-adhesion film through double embolic pathway on angiogenesis and overall survival (OS) time of VX2 liver cancer rabbits.

Chuanyu Yang, Zheng Xu, Kai Nie, Jing Liu

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Article in Translational cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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5 · Who and what money

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4 authors at 1 institution in 1 country.

Chuanyu YangDepartment of General Surgery, Affiliated Southeast Hospital of Xiamen University, Zhangzhou 363000, China.
Zheng XuDepartment of General Surgery, Affiliated Southeast Hospital of Xiamen University, Zhangzhou 363000, China.
Kai NieDepartment of General Surgery, Affiliated Southeast Hospital of Xiamen University, Zhangzhou 363000, China.
Jing LiuDepartment of General Surgery, Affiliated Southeast Hospital of Xiamen University, Zhangzhou 363000, China.
Zhongshan Hospital of Xiamen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCurcumin is a promising anti-tumor drug in recent years. The main function of absorbable anti-adhesion film is to prevent adhesions after surgical operation. The effects of curcumin-lipiodol emulsion injected via the hepatic artery and portal vein catheter combined with using absorbable anti-adhesion film around the liver angiogenesis are unknown. This article mainly discusses the effects of these combined strategies on the inhibition or reduction of postoperative angiogenesis and prolonging survival time of rabbit model.

methodsForty model rabbits with VX2 liver cancer were divided into four groups. Group A is the control group and its intervention is a simple lipiodol emulsion group. The intervention in group B was a simple lipiodol emulsion combined with an anti-adhesion membrane. The intervention in group C was a mixture of curcumin and lipiodol. The intervention in group D was a mixed emulsion of curcumin and lipiodol combined with an anti-adhesion membrane. The levels of aspartate aminotransferase (ALT) and alanine aminotransferase (AST) in the model rabbits were compared to analyze the damage of liver cells 1 day before embolization and 3, 7, 14 days after the embolization. In addition, the levels of vascular endothelial growth factor (VEGF) and microvessel density (MVD) in residual cancer tissues were determined by immunohistochemistry and Western blot. Finally, overall survival time (OS) of each group was recorded.

resultsThe results showed that the ALT and AST levels of venous blood before and after embolization in each group of rabbits were not changed significantly (P>0.05). The levels of VEGF and MVD in the group C and group D were lower than those in the group A (P<0.05). However, there was no significant difference between group B and group A (P>0.05). The decrease of VEGF and MVD in group D was most obvious, and group D had a significant difference compared with group C (P<0.05). Western blot analysis showed that the protein expression of VEGF was consistent with immunohistochemical staining. The overall survival (OS) time of group B showed no significant difference compared with group A (P>0.05). The OS time of group C and group D was longer than that of group A (P<0.05). Group D showed significantly difference on prolongation of the survival time than group C (P<0.05).

conclusionsOverall, the curcumin-lipiodol emulsion injected into the portal vein and hepatic artery supplying the tumor can significantly inhibit angiogenesis and play a role in prolonging the OS time of model rabbits. The application of anti-adhesion film alone cannot inhibit tumor angiogenesis and play a role in prolonging the OS time of model rabbits. However, curcumin-lipiodol emulsion combined with anti-adhesion film can obviously promote these effects.

Indexed as

Curcumin-lipiodol emulsionmicrovessel density (MVD)neovascularizationoverall survival (OS)rabbit VX2 liver cancer modelvascular endothelial growth factor (VEGF)

Identifiers

PMID35117420
PMCPMC8799229
OpenAlexW2995722419

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