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PHY906(KD018) an adjuvant based on a 1800-year-old Chinese medicine enhanced the anti-tumor activity of Sorafenib by changing the tumor microenvironment

机译:PHY906(KD018)是一种基于1800年历史的中药它通过改变肿瘤微环境来增强索拉非尼的抗肿瘤活性

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摘要

PHY906 (KD018) is a four-herb Chinese Medicine Formula. It has been shown to potentially enhance the therapeutic indices of different class anticancer agents in vivo. Here, PHY906 is reported to enhance the anti-tumor activity of Sorafenib in nude mice bearing HepG2 xenografts. Among the four herbal ingredients of PHY906, Scutellaria baicalensis Georgi (S) and Paeonia lactiflora Pall (P) are required; however, S plays a more important role than P in increasing tumor apoptosis induced by Sorafenib with an increase of mouse(m)FasL and human(h)FasR expression. PHY906 may potentiate Sorafenib action by increasing hMCP1 expression and enhancing infiltration of macrophages into tumors with a higher M1/M2 (tumor rejection) signature expression pattern, as well as affect autophagy by increasing AMPKα-P and ULK1-S555-P of tumors. Depletion of macrophage could counteract PHY906 to potentiate the anti-tumor activity of Sorafenib. It was reported that tumor cells with higher levels of ERK1/2-P are more susceptible to Sorafenib, and the S component of PHY906 may increase ERK1/2-P via inhibition of ERK1/2 phosphatase in HepG2 tumors. PHY906 may potentiate the anti-hepatoma activity of Sorafenib by multiple mechanisms targeting on the inflammatory state of microenvironment of tumor tissue through two major ingredients (P and S) of PHY906.
机译:PHY906(KD018)是一种四草药的中药配方。已经显示其潜在地增强了体内不同类别抗癌剂的治疗指数。在这里,据报道PHY906可以增强索拉非尼在荷HepG2异种移植裸鼠中的抗肿瘤活性。在PHY906的四种草药成分中,需要黄S(Scutellaria baicalensis Georgi(S))和Pa药(Paeonia lactiflora Pall)(P)。然而,随着小鼠(m)FasL和人类(h)FasR表达的增加,S在增加索拉非尼诱导的肿瘤凋亡中起着比P更重要的作用。 PHY906可以通过增加hMCP1表达并增强巨噬细胞向具有更高M1 / M2(肿瘤排斥)标记表达模式的肿瘤中的浸润来增强索拉非尼的作用,并通过增加肿瘤的AMPKα-P和ULK1-S555-P影响自噬。巨噬细胞的耗尽可以抵消PHY906增强索拉非尼的抗肿瘤活性。据报道,ERK1 / 2-P水平较高的肿瘤细胞对索拉非尼更敏感,而PHY906的S成分可能通过抑制HepG2肿瘤中的ERK1 / 2磷酸酶而增加ERK1 / 2-P。 PHY906可通过PHY906的两种主要成分(P和S)针对肿瘤组织微环境的炎症状态的多种机制来增强索拉非尼的抗肝癌活性。

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