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五价磷三(乙氧羰基)卟啉作为斑马鱼异种移植模型中治疗肝细胞癌的安全有效光敏剂

Phosphorus(V) Tris(ethoxycarbonyl)corrole As a Safe and Effective Photosensitizer for Hepatocellular Carcinoma Treatment in Zebrafish Xenograft Models.

作者信息

Liu Yan, Wang Liangliang, Lu Hao, Chen Rongrong, Zheng Kangdi, Zhang Zhao, Zhan Haiying, Zhang Haitao

机构信息

Department of Biochemistry and Molecular Biology, Guangdong Medical University, Zhanjiang 524023, China.

MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, Sun Yat-sen University, Guangzhou 510275, China.

出版信息

ACS Omega. 2025 Aug 18;10(34):38675-38685. doi: 10.1021/acsomega.5c03715. eCollection 2025 Sep 2.

Abstract

Corrole-based photosensitizers show great potential for tumor photodynamic therapy (PDT). While their photodynamic activity has been extensively studied at the cellular level, evaluation in mouse xenograft models remains challenging due to prolonged experimental timelines, complex drug administration, and high costs. To address these limitations, we developed a novel hepatocellular carcinoma model using wild-type AB zebrafish embryos as a xenograft platform. This model was employed to assess the antitumor efficacy, acute toxicity, and biodistribution of phosphorus-(V) tris-(ethoxycarbonyl)-corrole (-), an electron-deficient photosensitizer. Under red-light irradiation, - exhibited strong phototoxicity in zebrafish, inducing apoptosis in xenografted tumor cells. Biodistribution studies revealed - accumulation in the liver and digestive tract, demonstrating favorable tumor-targeting properties. Mechanistic investigations via qPCR indicated that -mediated PDT activated the c-JUN N-terminal kinase pathway, upregulated SIRT1 expression, and suppressed tumor cell proliferation. This work not only supports the therapeutic potential of corroles in hepatocellular carcinoma PDT but also establishes zebrafish as an efficient model for photosensitizer screening and mechanistic analysis, offering significant translational and research value.

摘要

基于咕啉的光敏剂在肿瘤光动力疗法(PDT)中显示出巨大潜力。虽然它们的光动力活性已在细胞水平上得到广泛研究,但由于实验时间长、药物给药复杂和成本高,在小鼠异种移植模型中的评估仍然具有挑战性。为了解决这些局限性,我们开发了一种新型的肝细胞癌模型,使用野生型AB斑马鱼胚胎作为异种移植平台。该模型用于评估缺电子光敏剂三(乙氧基羰基)磷(V)咕啉(-)的抗肿瘤疗效、急性毒性和生物分布。在红光照射下,-在斑马鱼中表现出强烈的光毒性,诱导异种移植肿瘤细胞凋亡。生物分布研究表明-在肝脏和消化道中积累,显示出良好的肿瘤靶向特性。通过qPCR进行的机制研究表明,-介导的PDT激活了c-JUN N端激酶途径,上调了SIRT1表达,并抑制了肿瘤细胞增殖。这项工作不仅支持咕啉在肝细胞癌PDT中的治疗潜力,还将斑马鱼确立为光敏剂筛选和机制分析的有效模型,具有重要的转化和研究价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/991f/12409558/8716e9d5f659/ao5c03715_0001.jpg

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