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热疗通过依赖 p53 的细胞凋亡选择性靶向宫颈肿瘤中的人乳头瘤病毒。

Hyperthermia Selectively Targets Human Papillomavirus in Cervical Tumors via p53-Dependent Apoptosis.

机构信息

Laboratory for Experimental Oncology and Radiobiology, Center for Experimental and Molecular Medicine, Amsterdam, the Netherlands. Department of Radiotherapy, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.

Department of Radiotherapy, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.

出版信息

Cancer Res. 2015 Dec 1;75(23):5120-9. doi: 10.1158/0008-5472.CAN-15-0816. Epub 2015 Nov 16.

Abstract

Human papillomavirus (HPV) is associated with cervical cancer, the third most common cancer in women. The high-risk HPV types 16 and 18 are found in over 70% of cervical cancers and produce the oncoprotein, early protein 6 (E6), which binds to p53 and mediates its ubiquitination and degradation. Targeting E6 has been shown to be a promising treatment option to eliminate HPV-positive tumor cells. In addition, combined hyperthermia with radiation is a very effective treatment strategy for cervical cancer. In this study, we examined the effect of hyperthermia on HPV-positive cells using cervical cancer cell lines infected with HPV 16 and 18, in vivo tumor models, and ex vivo-treated patient biopsies. Strikingly, we demonstrate that a clinically relevant hyperthermia temperature of 42 °C for 1 hour resulted in E6 degradation, thereby preventing the formation of the E6-p53 complex and enabling p53-dependent apoptosis and G2-phase arrest. Moreover, hyperthermia combined with p53 depletion restored both the cell-cycle distribution and apoptosis to control levels. Collectively, our findings provide new insights into the treatment of HPV-positive cervical cancer and suggest that hyperthermia therapy could improve patient outcomes.

摘要

人乳头瘤病毒(HPV)与宫颈癌有关,宫颈癌是女性中第三大常见癌症。高危型 HPV 16 和 18 型在超过 70%的宫颈癌中发现,产生癌蛋白早期蛋白 6(E6),它与 p53 结合并介导其泛素化和降解。靶向 E6 已被证明是消除 HPV 阳性肿瘤细胞的一种很有前途的治疗选择。此外,联合高热与放疗是宫颈癌非常有效的治疗策略。在这项研究中,我们使用感染 HPV 16 和 18 的宫颈癌细胞系、体内肿瘤模型和离体处理的患者活检,检查了高温对 HPV 阳性细胞的影响。引人注目的是,我们证明了临床相关的 42°C 高温 1 小时导致 E6 降解,从而防止 E6-p53 复合物的形成,并使 p53 依赖性凋亡和 G2 期阻滞。此外,高温联合 p53 耗竭使细胞周期分布和凋亡恢复到对照水平。总之,我们的发现为 HPV 阳性宫颈癌的治疗提供了新的见解,并表明热疗可能改善患者的预后。

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