Terry S. Elton
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
140
Citations
8,947
Est. group size
~7
Recurring co-author estimate
Active years
42
Publishing since 1985
Terry S. Elton studies how leukemia cells become resistant to chemotherapy drugs that target an enzyme called DNA topoisomerase II, which is important for how anticancer drugs like etoposide work. His lab uses techniques such as CRISPR/Cas9 gene editing and studies of RNA processing (including microRNAs and 'intronic polyadenylation,' a process affecting how genetic messages are cut and used) to understand and potentially reverse drug resistance in K562 human leukemia cells. This work aims to identify molecular mechanisms that could be targeted to make cancer drugs more effective for patients whose tumors have become resistant.
Publication output has remained modest and relatively steady over the last decade, with a peak of 6 papers in 2022 and averaging about 2 papers per year over the last five years.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Circumvention of acquired resistance to topoisomerase II-targeted anticancer agents in HL-60 leukemia cells by prevention of intronic polyadenylation
Journal of Pharmacology and Experimental Therapeutics · 2026
- Abrogation of Intronic Polyadenylation: CRISPR/Cas9-based Gene-editing to Circumvent Acquired Resistance to DNA Topoisomerase II-targeted Anticancer Agents (Abstract ID: 161640)
Journal of Pharmacology and Experimental Therapeutics · 2025
- Use of CRISPR/Cas9 with Homology-Directed Repair to Gene-Edit Topoisomerase II β in Human Leukemia K562 Cells: Generation of a Resistance Phenotype
Journal of Pharmacology and Experimental Therapeutics · 2024
- Circumvention of Topoisomerase IIα Intron 19 Intronic Polyadenylation in Acquired Etoposide-Resistant Human Leukemia K562 Cells
Molecular Pharmacology · 2024
- Strategies to Circumvent Topoisomerase IIα Intron 19 Intronic Polyadenylation (IPA) in Acquired Etoposide Resistance Human Leukemia K562 Cells
Journal of Pharmacology and Experimental Therapeutics · 2023
- Use of CRISPR/Cas9 with Homology-Directed Repair (HDR) to Gene-Edit Topoisomerase IIβ in Human Leukemia K562 Cells: Generation of a Resistance Phenotype
Journal of Pharmacology and Experimental Therapeutics · 2023
- Intronic Polyadenylation in Acquired Cancer Drug Resistance Circumvented by Utilizing CRISPR/Cas9 with Homology-Directed Repair: The Tale of Human DNA Topoisomerase IIα
Cancers · 2022
- Effects of hsa-miR-9-3p and hsa-miR-9-5p on Topoisomerase II β Expression in Human Leukemia K562 Cells with Acquired Resistance to Etoposide
Journal of Pharmacology and Experimental Therapeutics · 2022
- Maximizing the Efficacy of CRISPR/Cas Homology-Directed Repair Gene Targeting
IntechOpen eBooks · 2022
- Effects of hsa‐miR‐9‐3p and hsa‐miR‐9‐5p on Topoisomerase IIβ Expression in Human Leukemia K562 Cells with Acquired Resistance to Etoposide
The FASEB Journal · 2022
- CRISPR/Cas9 Genome Editing of the Human Topoisomerase IIα Intron 19 5′ Splice Site Circumvents Etoposide Resistance in Human Leukemia K562 Cells
Molecular Pharmacology · 2021
- CRISPR/Cas9 Genome Editing of the Human Topoisomerase IIα Intron‐19 5′ Splice Site Circumvents Etoposide Resistance in Human Leukemia K562 Cells
The FASEB Journal · 2021
- Effects of DNA topoisomerase IIα splice variants on acquired drug resistance
Cancer Drug Resistance · 2020
- miR‐9 as Post‐Transcriptional Modulator of DNA Topoisomerase IIα (TOP2α) in Human Leukemia K562 Cells with Acquired Resistance to the Anticancer Drug Etoposide
The FASEB Journal · 2019
- Alternative RNA Processing as a Determinant of Acquired Resistance to the Anticancer Drug Etoposide in Human Leukemia K562 Cells
The FASEB Journal · 2019
- Journal of Pharmacology and Experimental Therapeutics×7
- The FASEB Journal×5
- Molecular Pharmacology×4
- Cancer Research×2
- Cancers×1
- Audrey C. Kehling
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- GeunYoung Sim
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Jing Peng
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Ahmed Mansour
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
- Jun Wan
Biochemistry, Genetics and Molecular Biology · Indiana University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
Claim or correct this profile