• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

微血管密度基因特征的开发及其在精准医学中的应用。

Development of a Microvessel Density Gene Signature and Its Application in Precision Medicine.

作者信息

Kuronishi Megumi, Ozawa Yoichi, Kimura Takayuki, Li Shuyu Dan, Kato Yu

机构信息

Tsukuba Research Laboratories, Eisai Co., Ltd., Tsukuba, Japan.

Eisai Inc., Nutley, New Jersey.

出版信息

Cancer Res Commun. 2025 Mar 1;5(3):398-408. doi: 10.1158/2767-9764.CRC-24-0403.

DOI:10.1158/2767-9764.CRC-24-0403
PMID:39835481
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11880750/
Abstract

A novel gene signature for MVD was developed. This MVD gene score enables the estimation of MVD, reflecting the sensitivity to antiangiogenic inhibitors, in transcriptomic datasets. We demonstrated the utility of the MVD gene score together with a T cell-inflamed gene signature for potential future use as a clinical biomarker.

摘要

开发了一种用于微血管密度(MVD)的新型基因特征。这种MVD基因评分能够在转录组数据集中估计MVD,反映对抗血管生成抑制剂的敏感性。我们证明了MVD基因评分与T细胞炎症基因特征一起作为潜在临床生物标志物的未来用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0975/11880750/c33d731572f4/crc-24-0403_f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0975/11880750/b50d4f31a383/crc-24-0403_f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0975/11880750/ba17b93a6511/crc-24-0403_f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0975/11880750/a2c2f31ee8b9/crc-24-0403_f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0975/11880750/a16bad81ebc0/crc-24-0403_f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0975/11880750/c33d731572f4/crc-24-0403_f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0975/11880750/b50d4f31a383/crc-24-0403_f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0975/11880750/ba17b93a6511/crc-24-0403_f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0975/11880750/a2c2f31ee8b9/crc-24-0403_f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0975/11880750/a16bad81ebc0/crc-24-0403_f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0975/11880750/c33d731572f4/crc-24-0403_f5.jpg

相似文献

1
Development of a Microvessel Density Gene Signature and Its Application in Precision Medicine.微血管密度基因特征的开发及其在精准医学中的应用。
Cancer Res Commun. 2025 Mar 1;5(3):398-408. doi: 10.1158/2767-9764.CRC-24-0403.
2
A radiomics approach to assess tumour-infiltrating CD8 cells and response to anti-PD-1 or anti-PD-L1 immunotherapy: an imaging biomarker, retrospective multicohort study.一种基于放射组学的方法来评估肿瘤浸润 CD8 细胞与抗 PD-1 或抗 PD-L1 免疫治疗反应的关系:一项影像学生物标志物、回顾性多队列研究。
Lancet Oncol. 2018 Sep;19(9):1180-1191. doi: 10.1016/S1470-2045(18)30413-3. Epub 2018 Aug 14.
3
Development and Performance of a CD8 Gene Signature for Characterizing Inflammation in the Tumor Microenvironment across Multiple Tumor Types.CD8 基因特征的开发和性能,用于描述多种肿瘤类型肿瘤微环境中的炎症反应。
J Mol Diagn. 2021 Sep;23(9):1159-1173. doi: 10.1016/j.jmoldx.2021.06.002. Epub 2021 Jun 29.
4
Lenvatinib, an angiogenesis inhibitor targeting VEGFR/FGFR, shows broad antitumor activity in human tumor xenograft models associated with microvessel density and pericyte coverage.乐伐替尼是一种靶向VEGFR/FGFR的血管生成抑制剂,在与微血管密度和周细胞覆盖相关的人肿瘤异种移植模型中显示出广泛的抗肿瘤活性。
Vasc Cell. 2014 Sep 6;6:18. doi: 10.1186/2045-824X-6-18. eCollection 2014.
5
Tumor-agnostic transcriptome-based classifier identifies spatial infiltration patterns of CD8+T cells in the tumor microenvironment and predicts clinical outcome in early-phase and late-phase clinical trials.基于肿瘤无差异转录组的分类器可识别肿瘤微环境中 CD8+T 细胞的空间浸润模式,并预测早期和晚期临床试验的临床结局。
J Immunother Cancer. 2024 Apr 22;12(4):e008185. doi: 10.1136/jitc-2023-008185.
6
Effect of antiangiogenic therapy on tumor growth, vasculature and kinase activity in basal- and luminal-like breast cancer xenografts.抗血管生成治疗对基底样和腔面样乳腺癌异种移植瘤生长、血管生成和激酶活性的影响。
Mol Oncol. 2012 Aug;6(4):418-27. doi: 10.1016/j.molonc.2012.03.006. Epub 2012 Mar 31.
7
Focal adhesion kinase: an alternative focus for anti-angiogenesis therapy in ovarian cancer.黏着斑激酶:卵巢癌抗血管生成治疗的另一个靶点。
Cancer Biol Ther. 2014 Jul;15(7):919-29. doi: 10.4161/cbt.28882. Epub 2014 Apr 23.
8
Predicting Response to Standard First-line Treatment in High-grade Serous Ovarian Carcinoma by Angiogenesis-related Genes.通过血管生成相关基因预测高级别浆液性卵巢癌对标准一线治疗的反应
Anticancer Res. 2018 Sep;38(9):5393-5400. doi: 10.21873/anticanres.12869.
9
Relationship between HER2 expression and tumor interstitial angiogenesis in primary gastric cancer and its effect on prognosis.人表皮生长因子受体 2 表达与原发性胃癌间质血管生成的关系及其对预后的影响。
Pathol Res Pract. 2021 Jan;217:153280. doi: 10.1016/j.prp.2020.153280. Epub 2020 Nov 5.
10
Tumor endothelial marker 7 (TEM-7): a novel target for antiangiogenic therapy.肿瘤内皮标志物 7(TEM-7):一种新的抗血管生成治疗靶点。
Microvasc Res. 2011 Nov;82(3):253-62. doi: 10.1016/j.mvr.2011.09.004. Epub 2011 Sep 17.

本文引用的文献

1
Evaluation of potential biomarkers for lenvatinib plus pembrolizumab among patients with advanced endometrial cancer: results from Study 111/KEYNOTE-146.评估仑伐替尼联合帕博利珠单抗治疗晚期子宫内膜癌患者的潜在生物标志物:来自 Study 111/KEYNOTE-146 的结果。
J Immunother Cancer. 2024 Jan 19;12(1):e007929. doi: 10.1136/jitc-2023-007929.
2
Xerna™ TME Panel is a machine learning-based transcriptomic biomarker designed to predict therapeutic response in multiple cancers.Xerna™肿瘤微环境检测组合是一种基于机器学习的转录组生物标志物,旨在预测多种癌症的治疗反应。
Front Oncol. 2023 May 12;13:1158345. doi: 10.3389/fonc.2023.1158345. eCollection 2023.
3
The evolving tumor microenvironment: From cancer initiation to metastatic outgrowth.
不断演变的肿瘤微环境:从癌症起始到转移灶生长
Cancer Cell. 2023 Mar 13;41(3):374-403. doi: 10.1016/j.ccell.2023.02.016.
4
Multi-institutional Assessment of Pathologist Scoring HER2 Immunohistochemistry.多机构评估病理学家评分 HER2 免疫组化。
Mod Pathol. 2023 Jan;36(1):100032. doi: 10.1016/j.modpat.2022.100032.
5
Vascular endothelial cell development and diversity.血管内皮细胞的发育与多样性。
Nat Rev Cardiol. 2023 Mar;20(3):197-210. doi: 10.1038/s41569-022-00770-1. Epub 2022 Oct 5.
6
Molecular Mechanisms and Future Implications of VEGF/VEGFR in Cancer Therapy.血管内皮生长因子/血管内皮生长因子受体在癌症治疗中的分子机制及未来意义。
Clin Cancer Res. 2023 Jan 4;29(1):30-39. doi: 10.1158/1078-0432.CCR-22-1366.
7
Molecular correlates of clinical response and resistance to atezolizumab in combination with bevacizumab in advanced hepatocellular carcinoma.晚期肝细胞癌中阿替利珠单抗联合贝伐珠单抗治疗的临床反应和耐药的分子相关性。
Nat Med. 2022 Aug;28(8):1599-1611. doi: 10.1038/s41591-022-01868-2. Epub 2022 Jun 23.
8
Lenvatinib plus Pembrolizumab for Advanced Endometrial Cancer.仑伐替尼联合帕博利珠单抗治疗晚期子宫内膜癌。
N Engl J Med. 2022 Feb 3;386(5):437-448. doi: 10.1056/NEJMoa2108330. Epub 2022 Jan 19.
9
Relatlimab and Nivolumab versus Nivolumab in Untreated Advanced Melanoma.Relatlimab 和 Nivolumab 对比 Nivolumab 用于未经治疗的晚期黑色素瘤。
N Engl J Med. 2022 Jan 6;386(1):24-34. doi: 10.1056/NEJMoa2109970.
10
Reverse Translating Molecular Determinants of Anti-Programmed Death 1 Immunotherapy Response in Mouse Syngeneic Tumor Models.在小鼠同基因肿瘤模型中反向翻译抗程序性死亡 1 免疫治疗反应的分子决定因素。
Mol Cancer Ther. 2022 Mar 1;21(3):427-439. doi: 10.1158/1535-7163.MCT-21-0561.