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研究肺腺癌中的液-液相分离以提高预后准确性和治疗效果。

Investigating Liquid-Liquid Phase Separation in Lung Adenocarcinoma to Improve Prognostic Accuracy and Treatment Efficacy.

作者信息

Song Zipei, Li Yuting, Zhang Pengpeng, Wei Ke, Zhu Miaolin, Wang Yuheng, Li Zhihua, Chen Liang, Zheng Jianan

机构信息

Department of Thoracic Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

Department of Oncology, the First Medical Center, Chinese PLA General Hospital/Medical School of Chinese PLA, Beijing, China.

出版信息

J Cell Mol Med. 2025 Aug;29(16):e70807. doi: 10.1111/jcmm.70807.

Abstract

Liquid-Liquid Phase Separation (LLPS) refers to the separation of biomacromolecules into separate liquid phases within the cells, plays a critical role in lung cancer pathogenesis. Using machine learning, we developed an LLPS-associated signature (LLPSAS) based on 79 key genes. The LLPSAS demonstrated superior prognostic performance compared to 140 existing lung adenocarcinoma (LUAD) prognostic models. Patients stratified by LLPSAS risk scores revealed significantly lower overall survival in the high-risk group. Comparative analysis between the high-risk and low-risk groups showed distinct pathway enrichment, genomic alterations, tumour immune microenvironment (TIME) profiles, immunotherapy responses and drug sensitivities. The low-risk group exhibited an inflamed TIME, suggesting potentially better immunotherapy response. Furthermore, potential effective small molecule drugs were identified for high-risk patients. Finally, immunohistochemistry confirmed upregulation of LLPS-associated proteins (PLK1, HMMR, PRC1) in LUAD tissues, and immunofluorescence validated their LLPS occurrence. Conclusively, the LLPSAS provides a valuable tool for LUAD prognosis and treatment optimisation.

摘要

液-液相分离(LLPS)是指生物大分子在细胞内分离成不同的液相,在肺癌发病机制中起关键作用。我们利用机器学习,基于79个关键基因开发了一种LLPS相关特征(LLPSAS)。与140种现有的肺腺癌(LUAD)预后模型相比,LLPSAS显示出卓越的预后性能。根据LLPSAS风险评分分层的患者显示,高危组的总生存期显著更低。高危组和低危组之间的比较分析显示出不同的通路富集、基因组改变、肿瘤免疫微环境(TIME)特征、免疫治疗反应和药物敏感性。低危组表现出炎症性TIME,提示可能有更好的免疫治疗反应。此外,还为高危患者鉴定出了潜在有效的小分子药物。最后,免疫组织化学证实LUAD组织中LLPS相关蛋白(PLK1、HMMR、PRC1)上调,免疫荧光验证了它们的LLPS发生情况。总之,LLPSAS为LUAD的预后和治疗优化提供了一个有价值的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64fc/12372984/a6a2dcd1b968/JCMM-29-e70807-g005.jpg

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