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可释放奥沙利铂、多柔比星和吉西他滨的多靶点前药是肿瘤生长的强效抑制剂和免疫原性细胞死亡的有效诱导剂。

Multitargeting Prodrugs that Release Oxaliplatin, Doxorubicin and Gemcitabine are Potent Inhibitors of Tumor Growth and Effective Inducers of Immunogenic Cell Death.

作者信息

Sarkar Amrita, Novohradsky Vojtech, Maji Moumita, Babu Tomer, Markova Lenka, Kostrhunova Hana, Kasparkova Jana, Gandin Valentina, Brabec Viktor, Gibson Dan

机构信息

Institute for Drug Research, School of Pharmacy, The Hebrew University of Jerusalem, Jerusalem, 9112102, Israel.

Czech Academy of Sciences, Institute of Biophysics, Kralovopolska 135, 61200, Brno, Czech Republic.

出版信息

Angew Chem Int Ed Engl. 2023 Oct 16;62(42):e202310774. doi: 10.1002/anie.202310774. Epub 2023 Sep 12.

Abstract

A multitargeting prodrug (2) that releases gemcitabine, oxaliplatin, and doxorubicin in their active form in cancer cells is a potent cytotoxic agent with nM IC ; it is highly selective to cancer cells with mean selectivity indices to human (136) and murine (320) cancer cells. It effectively induces release of DAMPs (CALR, ATP & HMGB1) in CT26 cells facilitating more efficient phagocytosis by J774 macrophages than the FDA drugs or their co-administration. The viability of CT26 cells co-cultured with J774 macrophages and treated with 2 was reduced by 32 % compared to the non-treated cells, suggesting a synergistic antiproliferative effect between the chemical and immune reactions. 2 inhibited in vivo tumor growth in two murine models (LLC and CT26) better than the FDA drugs or their co-administration with significantly lower body weight loss. Mice inoculated with CT26 cells treated with 2 showed slightly better tumor free survival than doxorubicin.

摘要

一种多靶点前药(2),可在癌细胞中释放活性形式的吉西他滨、奥沙利铂和多柔比星,是一种具有纳摩尔IC的强效细胞毒剂;它对癌细胞具有高度选择性,对人(136)和鼠(320)癌细胞的平均选择性指数较高。它能有效诱导CT26细胞中DAMPs(钙网蛋白、ATP和高迁移率族蛋白B1)的释放,与FDA批准的药物或它们的联合给药相比,能促进J774巨噬细胞更有效地吞噬。与未处理的细胞相比,与J774巨噬细胞共培养并用2处理的CT26细胞的活力降低了32%,这表明化学和免疫反应之间存在协同抗增殖作用。在两种小鼠模型(LLC和CT26)中,2比FDA批准的药物或它们的联合给药更能有效抑制体内肿瘤生长,且体重减轻明显更低。接种用2处理的CT26细胞的小鼠比接受多柔比星治疗的小鼠显示出略好的无瘤生存期。

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