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重楼苷 D 诱导神经母细胞瘤细胞(IMR-32 和 LA-N-2)在小鼠体内发生坏死性凋亡。

Polyphyllin D induces necroptosis in neuroblastoma cells (IMR-32 and LA-N-2) in mice.

机构信息

Department of Pediatric Surgery, Fujita Health University Hospital, 1-98 Dengakugakubo, Kutsukake-Cho, Toyoake, Aichi Prefecture, 470-1192, Japan.

出版信息

Pediatr Surg Int. 2023 May 9;39(1):196. doi: 10.1007/s00383-023-05425-x.

Abstract

BACKGROUND

We previously reported that polyphyllin D, the main component of the traditional herbal medicinal Paris polyphylla, exhibited anticancer effects in vitro against human neuroblastoma cells. The aim of this investigation was to examine in vivo antitumor effects of polyphyllin D.

METHODS

Subcutaneous tumors were established in immune-deficient BALB/c nude mice using human neuroblastoma cell lines IMR-32 and LA-N-2. To evaluate the polyphyllin D activity, we used a mouse model of IMR-32 or LA-N-2 cell lines and analyzed subcutaneous tumors.

RESULTS

Subcutaneous tumor models were successfully established in mice using two human neuroblastoma cell lines. In the subcutaneous tumor model, porphyrin D was found to suppress tumor volume. We found that polyphyllin D suppressed the number of foci by Ki-67 staining (IMR-32 and LA-N-2; p < 0.01, 0.02, respectively). We found that polyphyllin D induces the RIPK3 expression, while polyphyllin D phosphorylates Ser358 in IMR-32 and Ser358 and Tyr376 in LA-N-2.

CONCLUSION

We developed a mouse model of subcutaneous tumors of neuroblastoma and demonstrated for the first time that polyphyllin D has an antitumor effect on neuroblastoma. Polyphyllin D can cause necroptosis depending on the cell type. The new drug can be expected by investigating a method to selectively induce cell death through the analysis of necroptosis.

摘要

背景

我们之前报道过,重楼属植物的主要成分重楼苷 D 对人神经母细胞瘤细胞具有体外抗癌作用。本研究旨在考察重楼苷 D 的体内抗肿瘤作用。

方法

用人神经母细胞瘤细胞系 IMR-32 和 LA-N-2 在免疫缺陷 BALB/c 裸鼠中建立皮下肿瘤。为了评估重楼苷 D 的活性,我们使用了 IMR-32 或 LA-N-2 细胞系的小鼠模型,并分析了皮下肿瘤。

结果

两种人神经母细胞瘤细胞系成功建立了小鼠皮下肿瘤模型。在皮下肿瘤模型中,重楼苷 D 被发现能抑制肿瘤体积。我们发现重楼苷 D 通过 Ki-67 染色抑制了焦点的数量(IMR-32 和 LA-N-2;p<0.01,0.02)。我们发现重楼苷 D 诱导 RIPK3 的表达,而重楼苷 D 在 IMR-32 中磷酸化 Ser358,在 LA-N-2 中磷酸化 Ser358 和 Tyr376。

结论

我们建立了神经母细胞瘤皮下肿瘤的小鼠模型,并首次证明重楼苷 D 对神经母细胞瘤具有抗肿瘤作用。重楼苷 D 可根据细胞类型引起坏死性凋亡。通过分析坏死性凋亡来选择性诱导细胞死亡的方法,有望开发出新的药物。

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