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局部注射 hsa-miR-634 治疗犬自发性恶性黑色素瘤肿瘤。

Therapeutic applications of local injection of hsa-miR-634 into canine spontaneous malignant melanoma tumors.

机构信息

Animal Medical Center, Gifu University, Gifu, Japan.

Department of Molecular Cytogenetics, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.

出版信息

Cancer Gene Ther. 2023 Nov;30(11):1524-1529. doi: 10.1038/s41417-023-00656-5. Epub 2023 Aug 8.

Abstract

Malignant melanoma (MM) is one of the most common tumors in both dogs and humans. As canine MM (CMM) and human MM (HMM) have similar clinical characteristics, CMM appears to be a good clinical model for HMM. We previously demonstrated that the introduction of a synthetic double-strand-microRNA-634 (miR-634) mimic triggered apoptotic cell death by directly targeting the genes associated with cytoprotective processes in various human cancer cell lines, including those of HMM. This study aimed to investigate the antitumor effects of the local administration of miR-634 on spontaneous CMMs to provide a basis for future applications of miR-634 formulations in HMM treatment. We found that miR-634 administration induced apoptosis in CMM cell lines in vitro via downregulation of Asct2, Nrf2, and survivin expression, similar to the mechanisms in HMM cell lines. Furthermore, intratumoral miR-634 administration induced antitumor effects in four of seven spontaneous CMM cases, with no adverse effects. Local administration of miR-634 to lung metastasis under ultrasound guidance induced tumor shrinkage. These results confirm the antitumor effect of the local administration of miR-634 in spontaneous CMM, a model for spontaneous HMM, thereby providing a novel treatment strategy for HMM.

摘要

恶性黑色素瘤(MM)是犬和人类中最常见的肿瘤之一。由于犬恶性黑色素瘤(CMM)和人类恶性黑色素瘤(HMM)具有相似的临床特征,因此 CMM 似乎是 HMM 的良好临床模型。我们之前的研究表明,引入合成双链 microRNA-634(miR-634)模拟物通过直接靶向与各种人类癌细胞系(包括 HMM 细胞系)中与细胞保护过程相关的基因,引发细胞凋亡。本研究旨在探讨 miR-634 局部给药对自发性 CMM 的抗肿瘤作用,为未来 miR-634 制剂在 HMM 治疗中的应用提供依据。我们发现,miR-634 给药通过下调 Asct2、Nrf2 和 survivin 的表达,在体外诱导 CMM 细胞系发生细胞凋亡,这与 HMM 细胞系的机制相似。此外,在 7 例自发性 CMM 病例中的 4 例中,肿瘤内 miR-634 给药诱导了抗肿瘤作用,且无不良反应。在超声引导下对肺转移瘤进行 miR-634 局部给药诱导肿瘤缩小。这些结果证实了 miR-634 局部给药对自发性 CMM(自发性 HMM 的模型)的抗肿瘤作用,从而为 HMM 提供了一种新的治疗策略。

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