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基于人类癌症转录组数据鉴定新型免疫治疗生物标志物的方案。

Protocol to identify novel immunotherapy biomarkers based on transcriptomic data in human cancers.

作者信息

Mei Jie, Cai Yun, Xu Rui, Zhu Yichao, Zhao Xinyuan, Zhang Yan, Mao Wenjun, Xu Junying, Yin Yongmei

机构信息

Department of Oncology, The Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi 214023, China; Department of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China; Wuxi Clinical College of Nanjing Medical University, Wuxi 214023, China.

Wuxi Clinical College of Nanjing Medical University, Wuxi 214023, China.

出版信息

STAR Protoc. 2023 Apr 28;4(2):102258. doi: 10.1016/j.xpro.2023.102258.

DOI:10.1016/j.xpro.2023.102258
PMID:37119142
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10173013/
Abstract

Immune checkpoint inhibitors have transformed the management of advanced cancers, but biomarkers for the prediction of therapeutic responses have not been fully uncovered. Here, we provide a step-by-step approach for the identification of novel biomarkers from public transcriptomic datasets. We comprehensively summarize the available transcriptomic datasets containing immunotherapy information and describe the necessary procedures to evaluate the effectiveness of a novel immunotherapy biomarker, which may accelerate the identification of novel immunotherapy biomarkers. For complete details on the use and execution of this protocol, please refer to Mei et al..

摘要

免疫检查点抑制剂已经改变了晚期癌症的治疗方式,但用于预测治疗反应的生物标志物尚未完全被发现。在此,我们提供了一种从公开的转录组数据集识别新型生物标志物的分步方法。我们全面总结了包含免疫治疗信息的可用转录组数据集,并描述了评估新型免疫治疗生物标志物有效性的必要程序,这可能会加速新型免疫治疗生物标志物的识别。有关本方案使用和执行的完整详细信息,请参考梅等人的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7870/10173013/ab40103e33fc/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7870/10173013/b4ed5753e950/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7870/10173013/a017d1fbf843/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7870/10173013/0110d64ce97a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7870/10173013/82ffe2390fee/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7870/10173013/cb24ffd9d929/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7870/10173013/eec4b0f1f302/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7870/10173013/ab40103e33fc/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7870/10173013/b4ed5753e950/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7870/10173013/a017d1fbf843/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7870/10173013/0110d64ce97a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7870/10173013/82ffe2390fee/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7870/10173013/cb24ffd9d929/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7870/10173013/eec4b0f1f302/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7870/10173013/ab40103e33fc/gr6.jpg

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Formin protein DIAPH1 positively regulates PD-L1 expression and predicts the therapeutic response to anti-PD-1/PD-L1 immunotherapy.
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Heliyon. 2024 Feb 24;10(5):e26604. doi: 10.1016/j.heliyon.2024.e26604. eCollection 2024 Mar 15.
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Anoikis-related gene signature is associated with immune infiltration and predicts the prognosis of non-small cell lung cancer.无锚定相关基因特征与免疫浸润相关,并可预测非小细胞肺癌的预后。
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