Vadimezan(DMXAA,AbMole,M1999)是一種多生物學(xué)活性的小分子化合物,其作用機(jī)理主要涉及三個(gè)方面:首先,Vadimezan(DMXAA)是一種STING激動(dòng)劑,可通過激活STING信號(hào)通路誘導(dǎo)I型干擾素分泌促進(jìn)免疫應(yīng)答;其次,
Vadimezan(DMXAA,AbMole,M1999)可競(jìng)爭(zhēng)性結(jié)合VEGFR2胞外結(jié)構(gòu)域,阻斷VEGF介導(dǎo)的血管生成信號(hào),因此常作為腫瘤研究中的血管破壞劑;最后,Vadimezan還可誘導(dǎo)細(xì)胞的凋亡
[1]。
AbMole為全球科研客戶提供高純度、高生物活性的抑制劑、細(xì)胞因子、人源單抗、天然產(chǎn)物、熒光染料、多肽、靶點(diǎn)蛋白、化合物庫、抗生素等科研試劑,全球大量文獻(xiàn)專利引用。
Vadimezan在腫瘤小鼠移植模型中表現(xiàn)出破壞腫瘤組織血管的活性,并降低腫瘤組織中的血液供給,這種作用在腫瘤組織中表現(xiàn)顯著,但對(duì)正常組織影響較小
[2]。例如Vadimezan與Simvastatin(MK 733)聯(lián)用,可顯著抑制B16-F10黑色素瘤小鼠模型中巨噬細(xì)胞(TAMs)介導(dǎo)的血管生成
[3]。此外,在EML4-ALK肺癌和CT26結(jié)腸癌模型中,DMXAA(Vadimezan)表現(xiàn)出顯著的遠(yuǎn)端效應(yīng)(abscopal effect),可促進(jìn)樹突細(xì)胞成熟
[4]。另一方面,Vadimezan(ASA-404)作為一種STING激動(dòng)劑還被廣泛用于研究先天免疫反應(yīng)
[5],特別是在小鼠為模型的動(dòng)物實(shí)驗(yàn)中,Vadimezan能促進(jìn)樹突細(xì)胞成熟和腫瘤抗原交叉呈遞,從而增強(qiáng)CD8
+ T細(xì)胞的浸潤和活性
[6],Vadimezan還可通過誘導(dǎo)腫瘤細(xì)胞免疫原性死亡(ICD)并釋放損傷相關(guān)分子模式(DAMPs)顯著增強(qiáng)機(jī)體對(duì)腫瘤細(xì)胞的免疫應(yīng)答。
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參考文獻(xiàn)及鳴謝
[1] Alan Huang, Yan Chen, Xiaoyan Li, et al., Molecular mechanistic study of ASA404 (vadimezan)-induced endothelial cell death, 70(8_Supplement) (2010) 4443-4443.
[2] A. Daei Farshchi Adli, R. Jahanban-Esfahlan, K. Seidi, et al., An overview on Vadimezan (DMXAA): The vascular disrupting agent, Chemical biology & drug design 91(5) (2018) 996-1006.
[3] V. F. Rauca, L. Patras, L. Luput, et al., Remodeling tumor microenvironment by liposomal codelivery of DMXAA and simvastatin inhibits malignant melanoma progression, Scientific reports 11(1) (2021) 22102.
[4] C. B. Synn, D. K. Kim, J. H. Kim, et al., Primary Tumor Suppression and Systemic Immune Activation of Macrophages through the Sting Pathway in Metastatic Skin Tumor, Yonsei medical journal 63(1) (2022) 42-55.
[5] Y. Xu, W. Li, X. Zhou, et al., Integrative Strategy for Investigating the Interactions between STING and Small-Molecule Ligands, Langmuir : the ACS journal of surfaces and colloids 38(46) (2022) 14185-14191.
[6] C. Zheng, W. Zhang, J. Wang, et al., Lenvatinib- and vadimezan-loaded synthetic high-density lipoprotein for combinational immunochemotherapy of metastatic triple-negative breast cancer, Acta pharmaceutica Sinica. B 12(9) (2022) 3726-3738.