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TSCRE: a comprehensive database for tumor-specific cis-regulatory elements
Guanjie Peng1,2,3, Bingyuan Liu1,2,3, Mohan Zheng2
1Clinical Big Data Research Center, Scientific Research Center, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen 518107, P.R. China.
Abstract:
Cis-regulatory elements (CREs) and super cis-regulatory elements (SCREs) are non-coding DNA regions which influence the transcription of nearby genes and play critical roles in development. Dysregulated CRE and SCRE activities have been reported to alter the expression of oncogenes and tumor suppressors, thereby regulating cancer hallmarks. To address the strong need for a comprehensive catalogue of dysregulated CREs and SCREs in human cancers, we present TSCRE (http://tscre.zsqylab.com/), an open resource providing tumor-specific and cell type-specific CREs and SCREs derived from the re-analysis of publicly available histone modification profiles. Currently, TSCRE contains 1 864 941 dysregulated CREs and 68 253 dysregulated SCREs identified from 1366 human patient samples spanning 17 different cancer types and 9 histone marks. Over 95% of these elements have been validated in public resources. TSCRE offers comprehensive annotations for each element, including associated genes, expression patterns, clinical prognosis, somatic mutations, transcript factor binding sites, cancer-type specificity, and drug response. Additionally, TSCRE integrates pathway and transcript factor enrichment analyses for each study, enabling in-depth functional and mechanistic investigations. Furthermore, TSCRE provides an interactive interface for users to explore any CRE and SCRE of interest. We believe TSCRE will be a highly valuable platform for the community to discover candidate cancer biomarkers.
Insights
The TSCRE database catalogs dysregulated cis-regulatory elements (CREs) and super cis-regulatory elements (SCREs) in human cancers. This resource aids in identifying novel cancer biomarkers and understanding gene regulation in tumors.
Area of Science:
- Genomics and Cancer Biology
- Non-coding DNA and Gene Regulation
Background:
- Cis-regulatory elements (CREs) and super cis-regulatory elements (SCREs) are crucial non-coding DNA regions controlling gene transcription and development.
- Altered CRE and SCRE activity is linked to oncogene and tumor suppressor dysregulation, impacting cancer progression.
- A comprehensive resource for dysregulated CREs and SCREs in human cancers is needed.
Purpose of the Study:
- To establish TSCRE, an open-access database cataloging tumor-specific and cell type-specific CREs and SCREs in human cancers.
- To provide a valuable platform for discovering candidate cancer biomarkers and investigating gene regulatory mechanisms.
Main Methods:
- Re-analysis of publicly available histone modification profiles from 1366 human patient samples across 17 cancer types.
- Identification and annotation of dysregulated CREs and SCREs using 9 histone marks.
- Integration of comprehensive annotations including gene associations, expression, mutations, and clinical data.
Main Results:
- TSCRE contains 1,864,941 dysregulated CREs and 68,253 dysregulated SCREs.
- Over 95% of identified elements are validated in public resources.
- The database offers detailed annotations and integrated pathway/transcription factor enrichment analyses.
Conclusions:
- TSCRE provides a comprehensive and validated resource for exploring dysregulated CREs and SCREs in human cancers.
- The platform facilitates in-depth functional investigations and the discovery of potential cancer biomarkers and therapeutic targets.
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