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揭示细胞衰老作为NF2相关前庭神经鞘瘤的治疗靶点。

Uncovering cellular senescence as a therapeutic target in NF2-related vestibular schwannoma.

作者信息

Franco-Caspueñas Sandra, García-Montoya Carmen, Contreras Julio, Lassaletta Luis, Varela-Nieto Isabel, Jiménez-Lara Ana M

机构信息

Neuropathology of Hearing and Myelinopathies Group. Institute for Biomedical Research Sols-Morreale, Spanish National Research Council, Autonomous University of Madrid (CSIC-UAM), 28029 Madrid, Spain; Rare Disease Network Biomedical Research Centre (CIBERER), Institute of Health Carlos III (ISCIII), 28029 Madrid, Spain; Hospital La Paz Institute for Health Research (IdiPAZ), 28046 Madrid, Spain.

Neuropathology of Hearing and Myelinopathies Group. Institute for Biomedical Research Sols-Morreale, Spanish National Research Council, Autonomous University of Madrid (CSIC-UAM), 28029 Madrid, Spain; Rare Disease Network Biomedical Research Centre (CIBERER), Institute of Health Carlos III (ISCIII), 28029 Madrid, Spain.

出版信息

Hear Res. 2025 Jan;455:109165. doi: 10.1016/j.heares.2024.109165. Epub 2024 Dec 4.

Abstract

BACKGROUND

Vestibular schwannomas (VS) are complex and heterogeneous human tumors arising from the Schwann cell compartment of the vestibulocochlear nerve. VS cause significant neurological deficit such as hearing loss and vestibular impairment, and in some cases death due to brainstem compression. There is an urgent need to find pharmacotherapies for VS since surgical removal and stereotactic radiosurgery are the only effective treatments. Cancer therapy based in the combination of drug-induced senescence and senolytics may provide an innovative pharmacological alternative for VS management.

METHODS

Senescence-associated β-galactosidase (SA-β-GAL) activity detection assay, real-time polymerase chain reaction (RT-PCR), western blotting and immunofluorescence, together with viability assays were used to analyze the response to different chemotherapy drugs of the human VS HEI-193 cell line. Human VS tumor paraffin sections were also studied for SA-β-GAL-stained cells.

RESULTS

We found that chemotherapy compounds induced genotoxic stress and cellular senescence in HEI-193 VS cells, as characterized by increased SA-β-GAL activity, growth arrest, increased levels of the cyclin-dependent kinase inhibitor p21 and the accumulation of DNA damage. These cellular senescence markers were also accompanied by an increase of senescence-associated secretory phenotype (SASP): IL6, IL8, IL1B and MMP1. Induction of senescence by chemotherapy rendered HEI-193 VS cells as druggable targets for senolytic compounds, as navitoclax. Thus, treatment with navitoclax selectively eliminated bleomycin-induced senescent HEI-193 VS cells by activating the extrinsic and intrinsic apoptosis pathways. Our data also show the presence of senescent cells, SA-β-GAL-positive stain, in human VS tumors, which are not present in healthy great auricular nerve sections.

CONCLUSIONS

These findings suggest that a one-two punch strategy of pro-senescence therapy induced by chemotherapy treatment followed by senolytic therapy represents a new paradigm for the pharmacological treatment of VS.

摘要

背景

前庭神经鞘瘤(VS)是起源于前庭蜗神经施万细胞区的复杂异质性人类肿瘤。VS会导致严重的神经功能缺损,如听力丧失和前庭功能障碍,在某些情况下还会因脑干受压而死亡。由于手术切除和立体定向放射外科是仅有的有效治疗方法,因此迫切需要找到针对VS的药物治疗方法。基于药物诱导衰老和衰老细胞溶解剂联合的癌症治疗可能为VS的管理提供一种创新的药理学替代方案。

方法

采用衰老相关β-半乳糖苷酶(SA-β-GAL)活性检测试验、实时聚合酶链反应(RT-PCR)、蛋白质免疫印迹法和免疫荧光法,以及活力测定法来分析人VS HEI-193细胞系对不同化疗药物的反应。还对人VS肿瘤石蜡切片进行了SA-β-GAL染色细胞研究。

结果

我们发现化疗化合物在HEI-193 VS细胞中诱导了基因毒性应激和细胞衰老,其特征为SA-β-GAL活性增加、生长停滞、细胞周期蛋白依赖性激酶抑制剂p21水平升高以及DNA损伤积累。这些细胞衰老标志物还伴随着衰老相关分泌表型(SASP)的增加:白细胞介素6(IL6)、白细胞介素8(IL8)、白细胞介素1β(IL1B)和基质金属蛋白酶1(MMP1)。化疗诱导的衰老使HEI-193 VS细胞成为衰老细胞溶解剂(如navitoclax)的可药物作用靶点。因此,用navitoclax治疗通过激活外源性和内源性凋亡途径选择性地消除了博来霉素诱导的衰老HEI-193 VS细胞。我们的数据还显示,在人VS肿瘤中存在衰老细胞(SA-β-GAL阳性染色),而在健康的耳大神经切片中不存在。

结论

这些发现表明,化疗诱导的促衰老治疗后再进行衰老细胞溶解治疗的“双拳出击”策略代表了VS药物治疗的新范式。

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