精准肿瘤学与分子癌症治疗综述数据集
关于精准肿瘤学、致癌信号通路和靶向治疗的综述文本数据集,涵盖TCGA和CCMI等计划的研究发现与机制讨论。

基本信息
资源简介
精准肿瘤学与分子癌症治疗综述数据集
【一句话概览】
本数据集是 figshare 公开的文本数据集,收录 8 个文件、合计 4.64 MB,主题涵盖 Gene Mutation、Cancer Genomics、p53、K-Ras、C-Myc,可用于医学自然语言处理(实体识别、信息抽取等),CC0 许可开放获取。
【数据集背景】
本数据集源站标题为《The Precision Oncology Approach to Molecular Cancer Therapeutics Targeting Oncogenic Signaling Pathways Is a Means to an End》。配套论文《<span>The Precision Oncology Approach to Molecular Cancer Therapeutics Targeting Oncogenic Signaling Pathways Is a Means to an End</span>》发表于 期刊(2024),DOI:10.2139/ssrn.4693638。源站首次发布:2025-06-08。
【数据内容】
源站原始描述:The TCGA Research Network started in 2005 has profiled and analyzed a large number of human tumors to discover molecular aberrations at the DNA, RNA, protein, and epigenetic levels and thereby provided reliable diagnostic and prognostic biomarkers for different cancer types since then. The presence of mutated genes is strongly correlated with cancer incidence, very specific causative genes or a small set of genes for most cancers have not been confirmed after decades of genomic studies. Nobel la…
【数据结构与技术规格】
文件数 8 个,合计 4.64 MB。Supplementary File 1.pdf:application/pdf,122.81 KB。Supplementary File 2.pdf:application/pdf,120.04 KB。Supplementary File 3.pdf:application/pdf,188.23 KB。数据集 DOI:10.6084/m9.figshare.28140365.v2。
【主题与分类】
源站学科分类:Cancer cell biology、Cancer diagnosis、Cancer genetics、Chemotherapy、Haematological tumours、Liquid biopsies。主题标签:Gene Mutation、Cancer Genomics、p53、K-Ras、C-Myc、Bcl-2、Cancer Stem Cells、Targeted Therapy、Immunotherapy、Precision Medicine。
【适用方向】
文本类数据可用于医学自然语言处理,如命名实体识别、信息抽取与文本分类。
【获取与许可】
源站页面:https://figshare.com/articles/dataset/_b_Precision_Oncology_Signaling_Pathways_Reprogramming_and_Targeted_Therapy_A_Holistic_Approach_to_Molecular_Cancer_Therapeutics_b_/28140365
使用许可:CC0(https://creativecommons.org/publicdomain/zero/1.0/)。
规范引用:Kumar, Manish (2025). The Precision Oncology Approach to Molecular Cancer Therapeutics Targeting Oncogenic Signaling Pathways Is a Means to an End. figshare. Dataset
下载信息
注册下载
需要注册 Kaggle 账号并登录后下载,适合需要跟踪下载记录和使用 API 的用户。
暂未开放公开下载
无需注册即可直接获取公开样本或文档,适合快速预览和评估数据集质量。
免登录有偿下载
公开数据集受托下载与技术交付服务。
提供高速下载与技术交付服务(收技术服务费,非数据销售)
暂未开放当前数据集主要来源为 Kaggle 公开托管,完整影像包建议通过原始链接或 Kaggle API 获取。
使用方式
数据集获取(Figshare)
- 源站标题:<b>The Precision Oncology Approach to Molecular Cancer Therapeutics Targeting Oncogenic Signaling Pathways Is a Means to an End</b>
- DOI:10.6084/m9.figshare.28140365.v2
- 发布日期:2025-06-08
- 文件数:8 个
- 文件总体积:4.64 MB
- 源站页面:https://figshare.com/articles/dataset/_b_Precision_Oncology_Signaling_Pathways_Reprogramming_and_Targeted_Therapy_A_Holistic_Approach_to_Molecular_Cancer_Therapeutics_b_/28140365
命令行下载
curl -L -o "Supplementary File 1.pdf" "https://ndownloader.figshare.com/files/51537047"
curl -L -o "Supplementary File 2.pdf" "https://ndownloader.figshare.com/files/51537050"
curl -L -o "Supplementary File 3.pdf" "https://ndownloader.figshare.com/files/51537053"
curl -L -o "Supplementary File 4.pdf" "https://ndownloader.figshare.com/files/51537056"
curl -L -o "Tables and Figures..pdf" "https://ndownloader.figshare.com/files/51537059"
curl -L -o "Cancer Genes.pdf" "https://ndownloader.figshare.com/files/51537062"
curl -L -o "The Precision Oncology Approach to Molecular Cancer Therapeutics Targeting Oncogenic Signaling Pathways Is a Means to an End_.pdf" "https://ndownloader.figshare.com/files/55206431"
curl -L -o "The Precision Oncology Approach to Molecular Cancer Therapeutics Targeting Oncogenic Signaling Pathways Is a Means to an End_.docx" "https://ndownloader.figshare.com/files/55206437"
文件清单
Supplementary File 1.pdf(122.81 KB)Supplementary File 2.pdf(120.04 KB)Supplementary File 3.pdf(188.23 KB)Supplementary File 4.pdf(193.21 KB)Tables and Figures..pdf(508.27 KB)Cancer Genes.pdf(418.39 KB)The Precision Oncology Approach to Molecular Cancer Therapeutics Targeting Oncogenic Signaling Pathways Is a Means to an End_.pdf(1.59 MB)The Precision Oncology Approach to Molecular Cancer Therapeutics Targeting Oncogenic Signaling Pathways Is a Means to an End_.docx(1.50 MB)
文件总体积 4.64 MB(源站 API 实测)。
数据说明
The TCGA Research Network started in 2005 has profiled and analyzed a large number of human tumors to discover molecular aberrations at the DNA, RNA, protein, and epigenetic levels and thereby provided reliable diagnostic and prognostic biomarkers for different cancer types since then. The presence of mutated genes is strongly correlated with cancer incidence, very specific causative genes or a small set of genes for most cancers have not been confirmed after decades of genomic studies. Nobel laureate James D. Watson opined at Cancer World 2013: "We can go ahead and sequence every piece of DNA that has ever existed, but I don’‘t think we’'ll find the Achilles heel of cancer. Importantly, it is not only necessary to associate genetic mutations with different cancers but also to work on the mechanism of action of mutagens by focusing on enzymes which could invariably mediate oncogenic transformations. For example, overexpression of the ribonucleotide reductase (RnR) enzyme which catalyzes the formation of deoxyribonucleotides from ribonucleotides necessary for cell division, is implicated in many forms of cancer and the genes for the components of the enzyme are often mutated, leading to hyperactivity of the enzyme. But there are instances indicating that cytoplasmic material rather than the karyoplast would be responsible for cellular transformation that might be better explained as a consequence of certain epigenetic modulation than purely genetic changes. RnR active site inhibitors have been developed accordingly to biophysically deactivate the enzyme when necessary, with positive results A comprehensive analysis of tumors based on their genomic studies must reveal the alterations in signaling pathways indicating patterns of vulnerabilities and the means to identify prospective targets for the development of personalized treatments and new combination therapies. In this regard, the Cancer Cell Map Initiative (CCMI), launched in 2015 by researchers at the University of California, San Francisco and the University of California, San Diego, allowed researchers to determine how hundreds of genetic mutations involved in a few types of cancer affect the activity of cer
许可
CC0
引用
学术使用请引用 DOI 10.6084/m9.figshare.28140365.v2(source: https://figshare.com/articles/dataset/_b_Precision_Oncology_Signaling_Pathways_Reprogramming_and_Targeted_Therapy_A_Holistic_Approach_to_Molecular_Cancer_Therapeutics_b_/28140365)。
数据缺失?
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