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一种表达凋亡素和蜂毒素基因的新型重组腺病毒可杀伤肝癌细胞并抑制异位肿瘤生长。

A novel recombinant adenovirus expressing apoptin and melittin genes kills hepatocellular carcinoma cells and inhibits the growth of ectopic tumor.

机构信息

Key Laboratory of Smart Breeding (Co-construction by Ministry and Province), Ministry of Agriculture and Rural Affairs, Tianjin Agricultural University, Tianjin, 300392, China.

Tianjin Key Laboratory of Agricultural Animal Breeding and Healthy Husbandry, College of Animal Science and Veterinary Medicine, Tianjin Agricultural University, Tianjin, 300392, China.

出版信息

Invest New Drugs. 2024 Aug;42(4):428-441. doi: 10.1007/s10637-024-01453-z. Epub 2024 Jun 27.

Abstract

HCC is the most common fatal malignancy. Although surgical resection is the primary treatment strategy, most patients are not eligible for resection due to tumor heterogeneity, underlying liver disease, or comorbidities. Therefore, this study explores the possibility of multi-molecular targeted drug delivery in treating HCC. In this study, we constructed the recombinant adenovirus co-expressing apoptin and melittin (MEL) genes. The inhibitory effect of the recombinant adenovirus on hepatocellular carcinoma cells was detected through experiments on cell apoptosis, migration, invasion, and other factors. The tumor inhibitory effect in vivo was assessed using subcutaneous HCC mice. Results showed that recombinant adenovirus co-expressing anti-tumor genes TAT and apoptin, RGD and MEL can significantly inhibit the proliferation, migration, and invasion of HCC cells by inducing an increase in reactive oxygen species (ROS) levels, upregulation of apoptotic proteins such as Bax, cleaved caspase-3, and cleaved caspase-9, and downregulation of the anti-apoptotic protein Bcl-2. In subcutaneous HCC mice, recombinant adenovirus induced significant apoptosis in tumor, and inhibited tumor growth. In conclusion, recombinant adenovirus co-expressing apoptin and MEL can inhibit the growth and proliferation of tumor cells both in vivo and in vitro.

摘要

HCC 是最常见的致命恶性肿瘤。虽然手术切除是主要的治疗策略,但由于肿瘤异质性、潜在的肝脏疾病或合并症,大多数患者不符合切除条件。因此,本研究探讨了多分子靶向药物递送治疗 HCC 的可能性。在这项研究中,我们构建了共表达凋亡素和蜂毒素 (MEL) 基因的重组腺病毒。通过细胞凋亡、迁移、侵袭等因素的实验,检测了重组腺病毒对肝癌细胞的抑制作用。通过皮下 HCC 小鼠评估了体内肿瘤抑制作用。结果表明,共表达抗肿瘤基因 TAT 和凋亡素、RGD 和 MEL 的重组腺病毒通过增加活性氧 (ROS) 水平,上调 Bax、裂解 caspase-3 和裂解 caspase-9 等凋亡蛋白,下调抗凋亡蛋白 Bcl-2,可显著抑制 HCC 细胞的增殖、迁移和侵袭。在皮下 HCC 小鼠中,重组腺病毒诱导肿瘤细胞发生明显凋亡,并抑制肿瘤生长。总之,共表达凋亡素和 MEL 的重组腺病毒可在体内和体外抑制肿瘤细胞的生长和增殖。

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