• 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

致癌性ACSM6损害膀胱癌中基于CD8 T细胞的免疫反应。

Oncogenic ACSM6 impairs CD8 T cell-based immune response in bladder cancer.

作者信息

Nie Zhenyu, Liu Bolong, Liu Jinhui, Zu Xiongbing, Wang Juanhua, Chen Jinbo, Fan Benyi, Deng Dingshan

机构信息

Department of Urology, Xiangya Hospital, Central South University, Changsha, China.

National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China.

出版信息

Biomark Res. 2024 Sep 27;12(1):112. doi: 10.1186/s40364-024-00657-y.

DOI:10.1186/s40364-024-00657-y
PMID:39334304
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11437728/
Abstract

Resistance to immunotherapy in bladder cancer has greatly limited its clinical application. Through single-cell sequencing, we determined that ACSM6, an oncogene that is highly expressed in bladder cancer, promotes the abilities of proliferation, cloning, migration, and invasion. The key point is that ACSM6 can also lead to a non-inflammatory immune microenvironment by inhibiting the chemotaxis and tumor killing ability of CD8 T cells. Survival analysis revealed that high ACSM6 expression was associated with shorter overall survival in the immunotherapy cohort. In summary, ACSM6 is expected to become a novel biomarker for predict bladder cancer progression.

摘要

膀胱癌对免疫疗法的耐药性极大地限制了其临床应用。通过单细胞测序,我们确定ACSM6(一种在膀胱癌中高表达的癌基因)可促进细胞增殖、克隆、迁移和侵袭能力。关键在于,ACSM6还可通过抑制CD8 T细胞的趋化性和肿瘤杀伤能力导致非炎症性免疫微环境。生存分析显示,在免疫治疗队列中,ACSM6高表达与总生存期较短相关。总之,ACSM6有望成为预测膀胱癌进展的新型生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afd7/11437728/81362ef745e9/40364_2024_657_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afd7/11437728/81362ef745e9/40364_2024_657_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afd7/11437728/81362ef745e9/40364_2024_657_Fig1_HTML.jpg

相似文献

1
Oncogenic ACSM6 impairs CD8 T cell-based immune response in bladder cancer.致癌性ACSM6损害膀胱癌中基于CD8 T细胞的免疫反应。
Biomark Res. 2024 Sep 27;12(1):112. doi: 10.1186/s40364-024-00657-y.
2
ACSM6 overexpression indicates a non-inflammatory tumor microenvironment and predicts treatment response in bladder cancer: results from multiple real-world cohorts.ACSM6过表达提示非炎症性肿瘤微环境并预测膀胱癌的治疗反应:来自多个真实世界队列的结果
Front Pharmacol. 2023 Jun 22;14:1222512. doi: 10.3389/fphar.2023.1222512. eCollection 2023.
3
S100A5 Attenuates Efficiency of Anti-PD-L1/PD-1 Immunotherapy by Inhibiting CD8 T Cell-Mediated Anti-Cancer Immunity in Bladder Carcinoma.S100A5 通过抑制 CD8 T 细胞介导的抗癌免疫来减弱抗 PD-L1/PD-1 免疫疗法在膀胱癌中的疗效。
Adv Sci (Weinh). 2023 Sep;10(25):e2300110. doi: 10.1002/advs.202300110. Epub 2023 Jul 6.
4
Bladder cancer intrinsic LRFN2 drives anticancer immunotherapy resistance by attenuating CD8 T cell infiltration and functional transition.膀胱癌内在的 LRFN2 通过减弱 CD8 T 细胞浸润和功能转化来驱动抗癌免疫治疗抵抗。
J Immunother Cancer. 2023 Oct;11(10). doi: 10.1136/jitc-2023-007230.
5
A novel CD8 T cell-related gene signature for predicting the prognosis and immunotherapy efficacy in bladder cancer.一种新型与 CD8 T 细胞相关的基因特征,可预测膀胱癌的预后和免疫治疗疗效。
Inflamm Res. 2023 Aug;72(8):1665-1687. doi: 10.1007/s00011-023-01772-6. Epub 2023 Aug 14.
6
Comprehensive pan-cancer analysis reveals NUSAP1 is a novel predictive biomarker for prognosis and immunotherapy response.全面泛癌分析揭示 NUSAP1 是一种新的预测预后和免疫治疗反应的生物标志物。
Int J Biol Sci. 2023 Sep 4;19(14):4689-4708. doi: 10.7150/ijbs.80017. eCollection 2023.
7
The prognostic marker KRT81 is involved in suppressing CD8 + T cells and predicts immunotherapy response for triple-negative breast cancer.预后标志物 KRT81 可抑制 CD8+T 细胞,并预测三阴性乳腺癌的免疫治疗反应。
Cancer Biol Ther. 2024 Dec 31;25(1):2355705. doi: 10.1080/15384047.2024.2355705. Epub 2024 May 22.
8
Immunological Hallmarks for Clinical Response to BCG in Bladder Cancer.膀胱癌对卡介苗临床反应的免疫学特征。
Front Immunol. 2021 Jan 29;11:615091. doi: 10.3389/fimmu.2020.615091. eCollection 2020.
9
Single-cell and bulk RNA-sequence identified fibroblasts signature and CD8 + T-cell - fibroblast subtype predicting prognosis and immune therapeutic response of bladder cancer, based on machine learning: bioinformatics multi-omics study.单细胞和批量 RNA 测序鉴定了成纤维细胞特征和 CD8+T 细胞-成纤维细胞亚型,基于机器学习:膀胱癌的生物信息学多组学研究预测预后和免疫治疗反应。
Int J Surg. 2024 Aug 1;110(8):4911-4931. doi: 10.1097/JS9.0000000000001516.
10
Fibronectin-1: A Predictive Immunotherapy Response Biomarker for Muscle‑Invasive Bladder Cancer.纤连蛋白 1:预测肌肉浸润性膀胱癌免疫治疗反应的生物标志物。
Arch Esp Urol. 2023 Feb;76(1):70-83. doi: 10.56434/j.arch.esp.urol.20237601.7.

引用本文的文献

1
Tumor-secreted RGS17 impairs CD8 + T cell function in lung adenocarcinoma through affecting glucose metabolism mediated by PI3K/AKT pathway.肿瘤分泌的RGS17通过影响PI3K/AKT途径介导的葡萄糖代谢来损害肺腺癌中CD8 + T细胞的功能。
Discov Oncol. 2025 Jul 8;16(1):1281. doi: 10.1007/s12672-025-02850-3.

本文引用的文献

1
Multi-organ immune-related adverse events from immune checkpoint inhibitors and their downstream implications: a retrospective multicohort study.免疫检查点抑制剂引起的多器官免疫相关不良事件及其下游影响:一项回顾性多队列研究。
Lancet Oncol. 2024 Aug;25(8):1053-1069. doi: 10.1016/S1470-2045(24)00278-X. Epub 2024 Jul 15.
2
A genome-wide association study of panicle blast resistance to in rice.水稻对穗瘟抗性的全基因组关联研究。
Mol Breed. 2024 Jul 11;44(7):49. doi: 10.1007/s11032-024-01486-5. eCollection 2024 Jul.
3
ACSM1 and ACSM3 Regulate Fatty Acid Metabolism to Support Prostate Cancer Growth and Constrain Ferroptosis.
ACSM1 和 ACSM3 通过调节脂肪酸代谢来支持前列腺癌的生长并抑制铁死亡。
Cancer Res. 2024 Jul 15;84(14):2313-2332. doi: 10.1158/0008-5472.CAN-23-1489.
4
ACSM6 overexpression indicates a non-inflammatory tumor microenvironment and predicts treatment response in bladder cancer: results from multiple real-world cohorts.ACSM6过表达提示非炎症性肿瘤微环境并预测膀胱癌的治疗反应:来自多个真实世界队列的结果
Front Pharmacol. 2023 Jun 22;14:1222512. doi: 10.3389/fphar.2023.1222512. eCollection 2023.
5
S100A5 Attenuates Efficiency of Anti-PD-L1/PD-1 Immunotherapy by Inhibiting CD8 T Cell-Mediated Anti-Cancer Immunity in Bladder Carcinoma.S100A5 通过抑制 CD8 T 细胞介导的抗癌免疫来减弱抗 PD-L1/PD-1 免疫疗法在膀胱癌中的疗效。
Adv Sci (Weinh). 2023 Sep;10(25):e2300110. doi: 10.1002/advs.202300110. Epub 2023 Jul 6.
6
Predictive biomarkers of immunotherapy response with pharmacological applications in solid tumors.免疫治疗反应的预测生物标志物及其在实体瘤中的药物应用。
Acta Pharmacol Sin. 2023 Sep;44(9):1879-1889. doi: 10.1038/s41401-023-01079-6. Epub 2023 Apr 13.
7
Neoadjuvant immunotherapy, chemotherapy, and combination therapy in muscle-invasive bladder cancer: A multi-center real-world retrospective study.新辅助免疫治疗、化疗和联合治疗在肌层浸润性膀胱癌中的应用:一项多中心真实世界回顾性研究。
Cell Rep Med. 2022 Nov 15;3(11):100785. doi: 10.1016/j.xcrm.2022.100785. Epub 2022 Oct 19.
8
Single-cell RNA sequencing highlights the role of inflammatory cancer-associated fibroblasts in bladder urothelial carcinoma.单细胞 RNA 测序强调了炎症性癌相关成纤维细胞在膀胱尿路上皮癌中的作用。
Nat Commun. 2020 Oct 8;11(1):5077. doi: 10.1038/s41467-020-18916-5.
9
A novel prognostic two-gene signature for triple negative breast cancer.一种用于三阴性乳腺癌的新型预后两基因标志物。
Mod Pathol. 2020 Nov;33(11):2208-2220. doi: 10.1038/s41379-020-0563-7. Epub 2020 May 13.
10
Precision medicine for urothelial bladder cancer: update on tumour genomics and immunotherapy.尿路上皮膀胱癌的精准医学:肿瘤基因组学和免疫治疗的最新进展。
Nat Rev Urol. 2018 Feb;15(2):92-111. doi: 10.1038/nrurol.2017.179. Epub 2017 Nov 14.