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光活化的多西环素前药靶向外泌体。

Photoactivatable Prodrug of Doxazolidine Targeting Exosomes.

机构信息

Molecular Pharmacology Program , Memorial Sloan Kettering Cancer Center , New York , New York 10065 , United States.

School of Pharmaceutical Sciences, Tsinghua University-Peking University Joint Center for Life Sciences , Tsinghua University , Beijing 100082 , China.

出版信息

J Med Chem. 2019 Feb 28;62(4):1959-1970. doi: 10.1021/acs.jmedchem.8b01508. Epub 2019 Feb 13.

Abstract

Natural lipid nanocarriers, exosomes, carry cell-signaling materials such as DNA and RNA for intercellular communications. Exosomes derived from cancer cells contribute to the progression and metastasis of cancer cells by transferring oncogenic signaling molecules to neighboring and remote premetastatic sites. Therefore, applying the unique properties of exosomes for cancer therapy has been expected in science, medicine, and drug discovery fields. Herein, we report that an exosome-targeting prodrug system, designated MARCKS-ED-photodoxaz, could spatiotemporally control the activation of an exquisitely cytotoxic agent, doxazolidine (doxaz), with UV light. The MARCKS-ED peptide enters a cell by forming a complex with the exosomes in situ at its plasma membrane and in the media. MARCKS-ED-photodoxaz releases doxaz under near-UV irradiation to inhibit cell growth with low nanomolar IC values. The MARCKS-ED-photodoxaz system targeting exosomes and utilizing photochemistry will potentially provide a new approach for the treatment of cancer, especially for highly progressive and invasive metastatic cancers.

摘要

天然脂质纳米载体外泌体携带 DNA 和 RNA 等细胞信号物质,用于细胞间通讯。癌细胞衍生的外泌体通过将致癌信号分子转移到邻近和远处的前转移部位,促进癌细胞的进展和转移。因此,在科学、医学和药物发现领域,人们一直期望利用外泌体的独特性质来进行癌症治疗。在此,我们报告了一种外泌体靶向前药系统,命名为 MARCKS-ED-photodoxaz,它可以利用紫外光时空控制高度细胞毒性药物(多西紫杉醇,doxaz)的激活。MARCKS-ED 肽通过在其质膜和介质中原位与外泌体形成复合物进入细胞。MARCKS-ED-photodoxaz 在近紫外光照射下释放多西紫杉醇,以低纳摩尔 IC 值抑制细胞生长。该外泌体靶向 MARCKS-ED-photodoxaz 系统和光化学的应用可能为癌症治疗,特别是高度进展和侵袭性转移性癌症的治疗提供一种新方法。

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