• 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

奥沙利铂相关lncRNAs预后模型可预测接受以奥沙利铂为基础化疗患者的预后。

Oxaliplatin related lncRNAs prognostic models predict the prognosis of patients given oxaliplatin-based chemotherapy.

作者信息

Zhou Qing-Nan, Lei Rong-E, Liang Yun-Xiao, Li Si-Qi, Guo Xian-Wen, Hu Bang-Li

机构信息

Department of Gastroenterology, The People's Hospital of Guangxi Zhuang Autonomous Region & Research center of Gastroenterology, Guangxi Academy of Medical Sciences, No. 6 Taoyuan Road, Nanning, 530021, Guangxi, China.

Department of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi, China.

出版信息

Cancer Cell Int. 2023 May 27;23(1):103. doi: 10.1186/s12935-023-02945-3.

DOI:10.1186/s12935-023-02945-3
PMID:37245016
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10223895/
Abstract

BACKGROUND

Oxaliplatin-based chemotherapy is the first-line treatment for colorectal cancer (CRC). Long noncoding RNAs (lncRNAs) have been implicated in chemotherapy sensitivity. This study aimed to identify lncRNAs related to oxaliplatin sensitivity and predict the prognosis of CRC patients underwent oxaliplatin-based chemotherapy.

METHODS

Data from the Genomics of Drug Sensitivity in Cancer (GDSC) was used to screen for lncRNAs related to oxaliplatin sensitivity. Four machine learning algorithms (LASSO, Decision tree, Random-forest, and support vector machine) were applied to identify the key lncRNAs. A predictive model for oxaliplatin sensitivity and a prognostic model based on key lncRNAs were established. The published datasets, and cell experiments were used to verify the predictive value.

RESULTS

A total of 805 tumor cell lines from GDSC were divided into oxaliplatin sensitive (top 1/3) and resistant (bottom 1/3) groups based on their IC50 values, and 113 lncRNAs, which were differentially expressed between the two groups, were selected and incorporated into four machine learning algorithms, and seven key lncRNAs were identified. The predictive model exhibited good predictions for oxaliplatin sensitivity. The prognostic model exhibited high performance in patients with CRC who underwent oxaliplatin-based chemotherapies. Four lncRNAs, including C20orf197, UCA1, MIR17HG, and MIR22HG, displayed consistent responses to oxaliplatin treatment in the validation analysis.

CONCLUSION

Certain lncRNAs were associated with oxaliplatin sensitivity and predicted the response to oxaliplatin treatment. The prognostic models established based on the key lncRNAs could predict the prognosis of patients given oxaliplatin-based chemotherapy.

摘要

背景

基于奥沙利铂的化疗是结直肠癌(CRC)的一线治疗方法。长链非编码RNA(lncRNAs)与化疗敏感性有关。本研究旨在鉴定与奥沙利铂敏感性相关的lncRNAs,并预测接受基于奥沙利铂化疗的CRC患者的预后。

方法

使用来自癌症药物敏感性基因组学(GDSC)的数据筛选与奥沙利铂敏感性相关的lncRNAs。应用四种机器学习算法(LASSO、决策树、随机森林和支持向量机)来鉴定关键lncRNAs。建立了奥沙利铂敏感性预测模型和基于关键lncRNAs的预后模型。使用已发表的数据集和细胞实验来验证预测价值。

结果

根据IC50值,将来自GDSC的总共805个肿瘤细胞系分为奥沙利铂敏感(前1/3)和耐药(后1/3)组,选择两组之间差异表达的113个lncRNAs并纳入四种机器学习算法,鉴定出七个关键lncRNAs。该预测模型对奥沙利铂敏感性表现出良好的预测能力。该预后模型在接受基于奥沙利铂化疗的CRC患者中表现出高性能。在验证分析中,包括C20orf197、UCA1、MIR17HG和MIR22HG在内的四个lncRNAs对奥沙利铂治疗表现出一致的反应。

结论

某些lncRNAs与奥沙利铂敏感性相关,并可预测对奥沙利铂治疗的反应。基于关键lncRNAs建立的预后模型可以预测接受基于奥沙利铂化疗患者的预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f99/10223895/42828b14262c/12935_2023_2945_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f99/10223895/bf95b8810136/12935_2023_2945_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f99/10223895/aefbba7c8a75/12935_2023_2945_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f99/10223895/18265416c6ca/12935_2023_2945_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f99/10223895/f857fe74bfe0/12935_2023_2945_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f99/10223895/b22e3c2a83da/12935_2023_2945_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f99/10223895/d6c7e3eb4306/12935_2023_2945_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f99/10223895/42828b14262c/12935_2023_2945_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f99/10223895/bf95b8810136/12935_2023_2945_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f99/10223895/aefbba7c8a75/12935_2023_2945_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f99/10223895/18265416c6ca/12935_2023_2945_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f99/10223895/f857fe74bfe0/12935_2023_2945_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f99/10223895/b22e3c2a83da/12935_2023_2945_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f99/10223895/d6c7e3eb4306/12935_2023_2945_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f99/10223895/42828b14262c/12935_2023_2945_Fig7_HTML.jpg

相似文献

1
Oxaliplatin related lncRNAs prognostic models predict the prognosis of patients given oxaliplatin-based chemotherapy.奥沙利铂相关lncRNAs预后模型可预测接受以奥沙利铂为基础化疗患者的预后。
Cancer Cell Int. 2023 May 27;23(1):103. doi: 10.1186/s12935-023-02945-3.
2
Upregulated lncRNA PRNT promotes progression and oxaliplatin resistance of colorectal cancer cells by regulating HIPK2 transcription.上调的长链非编码RNA PRNT通过调控HIPK2转录促进结肠癌细胞的进展和奥沙利铂耐药性。
World J Gastrointest Oncol. 2024 Apr 15;16(4):1564-1577. doi: 10.4251/wjgo.v16.i4.1564.
3
Identification and Validation of Six Autophagy-related Long Non-coding RNAs as Prognostic Signature in Colorectal Cancer.鉴定和验证六个自噬相关长非编码 RNA 作为结直肠癌的预后标志物。
Int J Med Sci. 2021 Jan 1;18(1):88-98. doi: 10.7150/ijms.49449. eCollection 2021.
4
The identification of CRNDE, H19, UCA1 and HOTAIR as the key lncRNAs involved in oxaliplatin or irinotecan resistance in the chemotherapy of colorectal cancer based on integrative bioinformatics analysis.基于整合生物信息学分析,鉴定 CRNDE、H19、UCA1 和 HOTAIR 作为涉及结直肠癌化疗中奥沙利铂或伊立替康耐药的关键 lncRNAs。
Mol Med Rep. 2019 Oct;20(4):3583-3596. doi: 10.3892/mmr.2019.10588. Epub 2019 Aug 14.
5
Construction and Validation of an Oxaliplatin-Resistant Gene Signature in Colorectal Cancer Patients Who Underwent Chemotherapy.接受化疗的结直肠癌患者中奥沙利铂耐药基因特征的构建与验证
Pharmaceuticals (Basel). 2022 Sep 13;15(9):1139. doi: 10.3390/ph15091139.
6
Identification of LncRNAs Associated With FOLFOX Chemoresistance in mCRC and Construction of a Predictive Model.mCRC中与FOLFOX化疗耐药相关的长链非编码RNA的鉴定及预测模型的构建
Front Cell Dev Biol. 2021 Jan 28;8:609832. doi: 10.3389/fcell.2020.609832. eCollection 2020.
7
LncRNA model predicts liver cancer drug resistance and validate experiments.长链非编码RNA模型预测肝癌耐药性并进行验证实验。
Front Cell Dev Biol. 2023 Apr 3;11:1174183. doi: 10.3389/fcell.2023.1174183. eCollection 2023.
8
Identification and Validation of Cuproptosis-Related LncRNA Signatures in the Prognosis and Immunotherapy of Clear Cell Renal Cell Carcinoma Using Machine Learning.基于机器学习的铜死亡相关 lncRNA 标志物在透明细胞肾细胞癌预后和免疫治疗中的鉴定和验证。
Biomolecules. 2022 Dec 16;12(12):1890. doi: 10.3390/biom12121890.
9
Characterization of sialylation-related long noncoding RNAs to develop a novel signature for predicting prognosis, immune landscape, and chemotherapy response in colorectal cancer.分析唾液酸化相关长非编码 RNA 以建立新型标志物预测结直肠癌患者的预后、免疫图谱和化疗反应
Front Immunol. 2022 Oct 18;13:994874. doi: 10.3389/fimmu.2022.994874. eCollection 2022.
10
Screening key lncRNAs with diagnostic and prognostic value for head and neck squamous cell carcinoma based on machine learning and mRNA-lncRNA co-expression network analysis.基于机器学习和 mRNA-lncRNA 共表达网络分析筛选具有诊断和预后价值的头颈鳞状细胞癌关键 lncRNAs。
Cancer Biomark. 2020;27(2):195-206. doi: 10.3233/CBM-190694.

引用本文的文献

1
Pan-cancer analysis of enhancer-induced MIR17HG and validation as a SIRT1-promoting factor in colorectal cancer.增强子诱导的MIR17HG的泛癌分析及其作为结直肠癌中促进SIRT1因子的验证
Med Oncol. 2025 Jun 30;42(8):299. doi: 10.1007/s12032-025-02841-y.
2
Development of a prognostic model for chemotherapy response and identification of TNFAIP2 as a target in colorectal cancer.结直肠癌化疗反应预后模型的建立及TNFAIP2作为靶点的鉴定。
Sci Rep. 2025 Jun 5;15(1):19858. doi: 10.1038/s41598-025-05556-2.
3
Emerging artificial intelligence-driven precision therapies in tumor drug resistance: recent advances, opportunities, and challenges.

本文引用的文献

1
Integrated analysis of necroptosis-related genes for evaluating immune infiltration and colon cancer prognosis.基于坏死性凋亡相关基因的综合分析评估免疫浸润和结肠癌预后。
Front Immunol. 2022 Dec 22;13:1085038. doi: 10.3389/fimmu.2022.1085038. eCollection 2022.
2
Construction of a Necroptosis-Related lncRNA Signature for Predicting Prognosis and Immune Response in Kidney Renal Clear Cell Carcinoma.构建坏死性凋亡相关长链非编码 RNA 标志物预测肾透明细胞癌的预后和免疫反应
Cells. 2022 Dec 23;12(1):66. doi: 10.3390/cells12010066.
3
Neoadjuvant therapy with immune checkpoint blockade, antiangiogenesis, and chemotherapy for locally advanced gastric cancer.
肿瘤耐药性中新兴的人工智能驱动的精准疗法:最新进展、机遇与挑战
Mol Cancer. 2025 Apr 23;24(1):123. doi: 10.1186/s12943-025-02321-x.
4
Review of the Different Outcomes Produced by Genetic Knock Out of the Long Non-coding microRNA-host-gene MIR22HG Pharmacologic Antagonism of its Intragenic microRNA product miR-22-3p.长链非编码微小RNA宿主基因MIR22HG基因敲除及其基因内微小RNA产物miR-22-3p的药理学拮抗作用所产生的不同结果综述
Microrna. 2025;14(1):19-41. doi: 10.2174/0122115366282339240604042154.
5
Multi-Omics Mining of lncRNAs with Biological and Clinical Relevance in Cancer.癌症中具有生物学和临床相关性的 lncRNAs 的多组学挖掘。
Int J Mol Sci. 2023 Nov 22;24(23):16600. doi: 10.3390/ijms242316600.
局部进展期胃癌的免疫检查点阻断、抗血管生成和化疗的新辅助治疗。
Nat Commun. 2023 Jan 3;14(1):8. doi: 10.1038/s41467-022-35431-x.
4
DDB2 represses epithelial-to-mesenchymal transition and sensitizes pancreatic ductal adenocarcinoma cells to chemotherapy.损伤特异性DNA结合蛋白2抑制上皮-间质转化并使胰腺导管腺癌细胞对化疗敏感。
Front Oncol. 2022 Dec 8;12:1052163. doi: 10.3389/fonc.2022.1052163. eCollection 2022.
5
Immediate surgery compared with short-course neoadjuvant gemcitabine plus capecitabine, FOLFIRINOX, or chemoradiotherapy in patients with borderline resectable pancreatic cancer (ESPAC5): a four-arm, multicentre, randomised, phase 2 trial.在可切除边缘的胰腺癌患者中,即刻手术与短程新辅助吉西他滨联合卡培他滨、FOLFIRINOX或放化疗的比较(ESPAC5):一项四臂、多中心、随机、2期试验
Lancet Gastroenterol Hepatol. 2023 Feb;8(2):157-168. doi: 10.1016/S2468-1253(22)00348-X. Epub 2022 Dec 12.
6
Determination of a DNA repair-related gene signature with potential implications for prognosis and therapeutic response in pancreatic adenocarcinoma.确定一种与DNA修复相关的基因特征,其对胰腺腺癌的预后和治疗反应可能具有潜在影响。
Front Oncol. 2022 Oct 24;12:939891. doi: 10.3389/fonc.2022.939891. eCollection 2022.
7
Long non-coding RNAs (lncRNAs) signaling in cancer chemoresistance: From prediction to druggability.长非编码 RNA(lncRNAs)在癌症化疗耐药性中的信号转导:从预测到可药性。
Drug Resist Updat. 2022 Dec;65:100866. doi: 10.1016/j.drup.2022.100866. Epub 2022 Sep 20.
8
Construction and Validation of an Oxaliplatin-Resistant Gene Signature in Colorectal Cancer Patients Who Underwent Chemotherapy.接受化疗的结直肠癌患者中奥沙利铂耐药基因特征的构建与验证
Pharmaceuticals (Basel). 2022 Sep 13;15(9):1139. doi: 10.3390/ph15091139.
9
Silenced LINC01134 Enhances Oxaliplatin Sensitivity by Facilitating Ferroptosis Through GPX4 in Hepatocarcinoma.沉默的LINC01134通过促进肝癌中GPX4介导的铁死亡增强奥沙利铂敏感性。
Front Oncol. 2022 Jul 8;12:939605. doi: 10.3389/fonc.2022.939605. eCollection 2022.
10
Clinical Evidence of Interaction between Nutraceutical Supplementation and Platinum-based Chemotherapy.营养保健品补充与铂类化疗之间相互作用的临床证据。
Curr Med Chem. 2023;30(19):2141-2164. doi: 10.2174/0929867329666220527120237.