研究动态
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蛋白质组学表明,肺腺癌的脑转移瘤在伽马刀放射外科手术中过度表达核糖体蛋白。

Proteomics shows that brain metastases of lung adenocarcinoma overexpress ribosomal proteins in response to gamma knife radiosurgery.

发表日期:2024 Jul 08
作者: Luqing Tong, Ke Ye, Qun Chen, Xiaoxi Wang, Chi Hu, Qingsheng Xu, Lihui Zhou, Renya Zhan, Ying Tong
来源: Brain Structure & Function

摘要:

许多指南推荐伽玛刀放射外科(GKRS)作为肺腺癌脑转移(LUAD)的一线治疗,但其具体机​​制尚不清楚。我们的目的是研究 LUAD 脑转移瘤响应 GKRS 超急性期的蛋白质组变化,并进一步探讨差异表达蛋白(DEP)的机制。癌症组织是在手术切除大脑转移瘤之前从新辅助立体定向放射外科临床试验中收集的(ChiCTR2000038995)。 GKRS 后 24 小时内收集 5 个 LUAD 脑转移组织。收集5例未接受放射治疗的脑转移组织作为对照样本。蛋白质组学分析显示,163 个蛋白质上调,25 个蛋白质下调。 GO和KEGG富集分析表明DEP与核糖体密切相关。 70 种核糖体蛋白中有 53 种显着过度表达,而没有一个表达不足。由7种上调核糖体蛋白(RPL4、RPS19、RPS16、RPLP0、RPS2、RPS26和RPS25)构建的风险评分是LUAD患者生存时间的独立危险因素。核糖体蛋白的过度表达可能代表对致命放射治疗的绝望反应。我们建议靶向抑制这些核糖体蛋白可能会增强 GKRS 的功效。© 2024。作者。
Gamma knife radiosurgery (GKRS) is recommended as the first-line treatment for brain metastases of lung adenocarcinoma (LUAD) in many guidelines, but its specific mechanism is unclear. We aimed to study the changes in the proteome of brain metastases of LUAD in response to the hyperacute phase of GKRS and further explore the mechanism of differentially expressed proteins (DEPs). Cancer tissues were collected from a clinical trial for neoadjuvant stereotactic radiosurgery before surgical resection of large brain metastases (ChiCTR2000038995). Five brain metastasis tissues of LUAD were collected within 24 h after GKRS. Five brain metastasis tissues without radiotherapy were collected as control samples. Proteomics analysis showed that 163 proteins were upregulated and 25 proteins were downregulated. GO and KEGG enrichment analyses showed that the DEPs were closely related to ribosomes. Fifty-three of 70 ribosomal proteins were significantly overexpressed, while none of them were underexpressed. The risk score constructed from 7 upregulated ribosomal proteins (RPL4, RPS19, RPS16, RPLP0, RPS2, RPS26 and RPS25) was an independent risk factor for the survival time of LUAD patients. Overexpression of ribosomal proteins may represent a desperate response to lethal radiotherapy. We propose that targeted inhibition of these ribosomal proteins may enhance the efficacy of GKRS.© 2024. The Author(s).