ResearcherThe University of Texas MD Anderson Cancer CenterNo recent work listed
David A. Boothman
Matched on ORCID iD 0000-0001-7474-9020; OpenAlex author ID A5016606481. Sources: funder_awards.
Their work
- Papers
- 7 (first author 0, last author 5)
- Trials
- 0
- Grants
- 2
- Labs led
- 1
- Collaborators
- 18
2011: 1 paper · 2012: 1 grant · 2013: none · 2014: 1 grant · 2015: 4 papers · 2016: none · 2017: 2 papers
Papers 7
- Using a novel NQO1 bioactivatable drug, beta-lapachone (ARQ761), to enhance chemotherapeutic effects by metabolic modulation in pancreatic cancer. Last author DOI 10.1002/jso.24624↗
- The NQO1 bioactivatable drug, β-lapachone, alters the redox state of NQO1+ pancreatic cancer cells, causing perturbation in central carbon metabolism. Co-author DOI 10.1074/jbc.m117.813923↗
- NAMPT inhibition sensitizes pancreatic adenocarcinoma cells to tumor-selective, PAR-independent metabolic catastrophe and cell death induced by β-lapachone. Last author DOI 10.1038/cddis.2014.564↗
- Tumor-selective use of DNA base excision repair inhibition in pancreatic cancer using the NQO1 bioactivatable drug, β-lapachone. Last author DOI 10.1038/srep17066↗
- Fibulin-5 Blocks Microenvironmental ROS in Pancreatic Cancer. Co-author DOI 10.1158/0008-5472.can-15-0744↗
- Targeting glutamine metabolism sensitizes pancreatic cancer to PARP-driven metabolic catastrophe induced by ß-lapachone. Last author DOI 10.1186/s40170-015-0137-1↗
- Modulating endogenous NQO1 levels identifies key regulatory mechanisms of action of β-lapachone for pancreatic cancer therapy. Last author DOI 10.1158/1078-0432.ccr-10-1983↗
Grants 2
Closest collaborators
The 18 strongest of 18 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Zachary Moore · 4 shared papers, 2015 · strength 0.18
- Paper NAMPT inhibition sensitizes pancreatic adenocarcinoma cells to tumor-selective, PAR-independent metabolic catastrophe a… DOI 10.1038/cddis.2014.564↗
- Paper Fibulin-5 Blocks Microenvironmental ROS in Pancreatic Cancer. DOI 10.1158/0008-5472.can-15-0744↗
- Paper Tumor-selective use of DNA base excision repair inhibition in pancreatic cancer using the NQO1 bioactivatable drug, β-l… DOI 10.1038/srep17066↗
- Molly A. Silvers · 3 shared papers, 2015–2017 · strength 0.17
- Paper The NQO1 bioactivatable drug, β-lapachone, alters the redox state of NQO1+ pancreatic cancer cells, causing perturbatio… DOI 10.1074/jbc.m117.813923↗
- Paper Using a novel NQO1 bioactivatable drug, beta-lapachone (ARQ761), to enhance chemotherapeutic effects by metabolic modul… DOI 10.1002/jso.24624↗
- Paper Tumor-selective use of DNA base excision repair inhibition in pancreatic cancer using the NQO1 bioactivatable drug, β-l… DOI 10.1038/srep17066↗
- Gaurab Chakrabarti · 3 shared papers, 2015 · strength 0.13
- Paper NAMPT inhibition sensitizes pancreatic adenocarcinoma cells to tumor-selective, PAR-independent metabolic catastrophe a… DOI 10.1038/cddis.2014.564↗
- Paper Tumor-selective use of DNA base excision repair inhibition in pancreatic cancer using the NQO1 bioactivatable drug, β-l… DOI 10.1038/srep17066↗
- Paper Targeting glutamine metabolism sensitizes pancreatic cancer to PARP-driven metabolic catastrophe induced by ß-lapachone. DOI 10.1186/s40170-015-0137-1↗
- Muhammad Shaalan Beg · 2 shared papers, 2017 · strength 0.13
- Paper The NQO1 bioactivatable drug, β-lapachone, alters the redox state of NQO1+ pancreatic cancer cells, causing perturbatio… DOI 10.1074/jbc.m117.813923↗
- Paper Using a novel NQO1 bioactivatable drug, beta-lapachone (ARQ761), to enhance chemotherapeutic effects by metabolic modul… DOI 10.1002/jso.24624↗
- Matthew E. Merritt · 2 shared papers, 2017 · strength 0.13
- Paper The NQO1 bioactivatable drug, β-lapachone, alters the redox state of NQO1+ pancreatic cancer cells, causing perturbatio… DOI 10.1074/jbc.m117.813923↗
- Paper Using a novel NQO1 bioactivatable drug, beta-lapachone (ARQ761), to enhance chemotherapeutic effects by metabolic modul… DOI 10.1002/jso.24624↗
- Rolf A. Brekken · 3 shared papers, 2011–2015 · strength 0.12
- Paper NAMPT inhibition sensitizes pancreatic adenocarcinoma cells to tumor-selective, PAR-independent metabolic catastrophe a… DOI 10.1038/cddis.2014.564↗
- Paper Fibulin-5 Blocks Microenvironmental ROS in Pancreatic Cancer. DOI 10.1158/0008-5472.can-15-0744↗
- Paper Modulating endogenous NQO1 levels identifies key regulatory mechanisms of action of β-lapachone for pancreatic cancer t… DOI 10.1158/1078-0432.ccr-10-1983↗
- Xiumei Huang · 1 shared paper, 2017 · strength 0.06
- Daniel A. Laheru · 1 shared paper, 2017 · strength 0.06
- Mary Topalovski · 1 shared paper, 2015 · strength 0.05
- Miao Wang · 1 shared paper, 2015 · strength 0.05
- Huamin Wang · 1 shared paper, 2015 · strength 0.05
- Agnieszka Katarzyna Witkiewicz · 1 shared paper, 2015 · strength 0.05
- Lewis C. Cantley · 1 shared paper, 2015 · strength 0.04
- Stanton L. Gerson · 1 shared paper, 2015 · strength 0.04
- Alec C. Kimmelman · 1 shared paper, 2015 · strength 0.04
- Costas Andreas Lyssiotis · 1 shared paper, 2015 · strength 0.04
- Long Shan Li · 1 shared paper, 2011 · strength 0.02
- Carlton C. Barnett · 1 shared paper, 2011 · strength 0.02
How to reach this person
A chain of introductions through people who have published, run trials or held grants together (warm_path@1: fewest links first, then the strongest). Built from public records only; no contact details are kept.