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在舌癌动物模型中,围手术期靶向缺氧诱导因子1α(HIF1α)可提高术后生存率。

Targeting HIF1α peri-operatively increased post-surgery survival in a tongue cancer animal model.

作者信息

Ahn Soon-Hyun, Choi Joo Yeon, Kim Dong Wook, Lee Doh Young, Jeon Eun-Hui, Jeong Woo-Jin, Paik Jin Ho

机构信息

Department of Otorhinolaryngology Head and Neck Surgery, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam-si, South Korea,

出版信息

Ann Surg Oncol. 2015 Sep;22(9):3041-8. doi: 10.1245/s10434-014-4323-0. Epub 2015 Jan 7.

Abstract

BACKGROUND

The purpose of the present study was to evaluate the relationship between hypoxia-inducible factor 1 alpha subunit (HIF1α) and tumor initiation in squamous cell carcinoma cell lines and whether targeting HIF1α perioperatively might exert positive effects on survival or recurrence in an animal model.

METHODS

The expression of HIF1α and tumorigenic potential in nude mice was compared using human head and neck squamous cell carcinoma cell lines (SNU1041, SNU1066, SNU1076, PCI01, PCI13, PCI50). A recurrent tongue cancer model was established by first injecting tumor cells in the lateral tongue and then excising the tongue masses for replanting in the neck. The effect of HIF1α inhibitors was assessed using this animal model.

RESULTS

We observed good correlation between tumorigenic potential and HIF1α nuclear expression in the cell lines tested. Furthermore, knockdown of HIF1α inhibited tumor growth in the animal model. After in vitro testing of five HIF1α inhibitors, echinomycin and LAQ824 were selected for the animal study. Pre- and postoperative treatment with echinomycin showed significant improvement in postsurgery survival and recurrence.

CONCLUSIONS

Our results suggested that adjuvant targeting of HIF1α before and after surgery could be a new targeted therapy strategy for squamous cell carcinoma.

摘要

背景

本研究旨在评估缺氧诱导因子1α亚基(HIF1α)与鳞状细胞癌细胞系中肿瘤起始之间的关系,以及围手术期靶向HIF1α是否可能对动物模型的生存或复发产生积极影响。

方法

使用人头颈部鳞状细胞癌细胞系(SNU1041、SNU1066、SNU1076、PCI01、PCI13、PCI50)比较裸鼠中HIF1α的表达和致瘤潜力。通过先将肿瘤细胞注射到舌外侧,然后切除舌肿块并重新种植到颈部来建立复发性舌癌模型。使用该动物模型评估HIF1α抑制剂的效果。

结果

我们在所测试的细胞系中观察到致瘤潜力与HIF1α核表达之间具有良好的相关性。此外,敲低HIF1α可抑制动物模型中的肿瘤生长。在对五种HIF1α抑制剂进行体外测试后,选择了棘霉素和LAQ824进行动物研究。棘霉素术前和术后治疗均显示术后生存和复发有显著改善。

结论

我们的结果表明,手术前后辅助靶向HIF1α可能是鳞状细胞癌的一种新的靶向治疗策略。

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