TEDEdb: A multicohort analysis and resource for transposable element differential expression in cancer
6 affiliations
- 1Coriell Institute for Medical Research, Camden, NJ 08103
- 2Center for Computational and Integrative Biology, Rutgers University, Camden, NJ 08103
- 3Department of Computer Science, Rutgers University, Camden, NJ 08103
- 4Rutgers Cancer Institute, Rutgers University, New Brunswick, NJ 08901
- 5The Wistar Institute of Anatomy and Biology, Philadelphia, PA 19104
- 6Cooper Medical School at Rowan University, Camden, NJ 08103
Abstract
The human genome consists of nearly 50% repetitive DNA, referred to for decades as “junk DNA.” These repetitive sequences, usually under the strict control of epigenetic silencing, can become aberrantly expressed in cancer. Some of these expressed sequences, e.g., transposable elements (TEs), can induce innate immune responses when derepressed following treatment with epigenetic therapies. As a result, epigenetic therapy has been suggested to augment cancer therapies. TEs are traditionally ignored in most RNA-seq studies and their expression is often excluded from publicly available data sources. Thus, the vast amount of publicly available RNA-seq data is an untapped resource for exploring the role of TE expression in cancer and cancer treatment. Here, we present a uniform reanalysis of over 7,000 RNA-seq samples, encompassing more than 2,000 differential expression experiments across 220 cancer cell lines and 700 drug treatments. We observed that TE expression is more prone to batch effects than gene expression alone, necessitating the use of meta-analysis techniques to probe the dataset for global trends. We confirm that DNMTi and HDACis are powerful inducers of TE expression. We also show that nonepigenetic compounds such as cyclin-dependent kinase and topoisomerase inhibitors can also induce robust up-regulation of TE-derived repetitive DNA elements and confirm that this induction is consistent with transcriptional signatures of viral mimicry response. We made all data available through a publicly available database called the Transposable Element Differential Expression Database, or TEDEdb, and created an interactive web application for its exploration located at https://dataexplorer.coriell.org/TEDEdb/
Related
- Transposable element DNA and RNA: Drivers of gene expression, evolution, and disease
- Comprehensive characterization of transposable element expression reveals regulatory circuitry and clinical implications in cancers
- Transposable element-mediated structural variations shape gene expression and agronomic trait diversity in Brassica napus
- Near-complete genome assembly of the African turquoise killifish enables locus-level profiling of transposable element expression
- Landscape of transposable element polymorphism across geographically diverse samples of the grasshopper Trilophidia annulata
BibTeX
@article{calendo2026tededb,
title = {{TEDEdb: A multicohort analysis and resource for transposable element differential expression in cancer}},
author = {Gennaro Calendo and Morgan Chaunzwa and Iman Dehzangi and Jozef Madzo and Jean-Pierre J. Issa},
journal = {Proceedings of the National Academy of Sciences of the United States of America},
year = {2026},
month = oct,
doi = {10.1073/pnas.2615533123},
url = {https://doi.org/10.1073/pnas.2615533123},
note = {CC BY-NC-ND 4.0},
}
RIS
TY - JOUR
TI - TEDEdb: A multicohort analysis and resource for transposable element differential expression in cancer
AU - Gennaro Calendo
AU - Morgan Chaunzwa
AU - Iman Dehzangi
AU - Jozef Madzo
AU - Jean-Pierre J. Issa
PY - 2026
DA - 2026/10/28
JO - Proceedings of the National Academy of Sciences of the United States of America
DO - 10.1073/pnas.2615533123
UR - https://doi.org/10.1073/pnas.2615533123
AB - The human genome consists of nearly 50% repetitive DNA, referred to for decades as “junk DNA.” These repetitive sequences, usually under the strict control of epigenetic silencing, can become aberrantly expressed in cancer. Some of these expressed sequences, e.g., transposable elements (TEs), can induce innate immune responses when derepressed following treatment with epigenetic therapies. As a result, epigenetic therapy has been suggested to augment cancer therapies. TEs are traditionally ignored in most RNA-seq studies and their expression is often excluded from publicly available data sources. Thus, the vast amount of publicly available RNA-seq data is an untapped resource for exploring the role of TE expression in cancer and cancer treatment. Here, we present a uniform reanalysis of over 7,000 RNA-seq samples, encompassing more than 2,000 differential expression experiments across 220 cancer cell lines and 700 drug treatments. We observed that TE expression is more prone to batch effects than gene expression alone, necessitating the use of meta-analysis techniques to probe the dataset for global trends. We confirm that DNMTi and HDACis are powerful inducers of TE expression. We also show that nonepigenetic compounds such as cyclin-dependent kinase and topoisomerase inhibitors can also induce robust up-regulation of TE-derived repetitive DNA elements and confirm that this induction is consistent with transcriptional signatures of viral mimicry response. We made all data available through a publicly available database called the Transposable Element Differential Expression Database, or TEDEdb, and created an interactive web application for its exploration located at https://dataexplorer.coriell.org/TEDEdb/
SN - 0027-8424
SN - 1091-6490
ER -