精准肿瘤学、信号通路重编程和靶向治疗:一种整体性的分子癌症治疗方法

包含一篇综述精准肿瘤学与靶向治疗的文章,涵盖癌症分子机制和个体化治疗。

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DataCite Commons
2025-06-08 更新
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文本Gene MutationCancer Genomicsp53K-RasC-MycBcl-2Cancer Stem CellsTargeted TherapyImmunotherapyPrecision Medicine
Precision Oncology, Signaling Pathways Reprogramming and Targeted Therapy: A Holistic Approach to Molecular Cancer Therapeutics

基本信息

模态
文本
大小
0.004639944 GB
许可
CC0
创建/更新时间
2025-06-08
版本
v2

资源简介

精准肿瘤学、信号通路重编程和靶向治疗:一种整体性的分子癌症治疗方法

【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

官方服务

专家保障全链路合规授权与标注交付

陕川双基地 × 超十家三甲医院直连

从合规授权、采集治理、专业标注到数据集交付,我们提供全链路闭环服务,让高质量临床数据即拿即用。

⚡️ 需要原始数据或标注支持?联系我们获取定制方案。

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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)

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?

依托陕西、四川两大基地,我们与超过十家三甲医院建立直接合作关系,覆盖合规授权、采集治理、专业标注、数据交付的全流程,为AI医疗团队提供即拿即用的高质量临床数据。

⚡️ 需要数据支持或标注服务?立即联系我们获取专业方案。

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