David P. Douglass
Sourced from institutional research profiles (UAMS TRI or ARA).
Associate Professor
Peds Pediatrics, College of Medicine
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
David P. Douglass studies pediatric cancers, with a focus on sarcomas and neuroblastoma. His research investigates novel therapeutic strategies, including the development of prognostic signatures and the evaluation of new agents. Douglass has published work on the role of pharmacotherapeutic agents in desmoid tumors and the clinical features of low-grade non-rhabdomyosarcoma soft tissue sarcomas. He has also explored molecular mechanisms in fusion-positive rhabdomyosarcoma and identified potential therapeutic targets, such as CDK9, for neuroblastoma and rhabdomyosarcoma. His collaborators include Kimo C. Stine, Varsha G. Desai, Vikrant Vijay, and James C. Fuscoe.
Metrics
- h-index: 3
- Publications: 12
- Citations: 22
Positions
-
Associate Professor 2025–presentUniversity of Arkansas for Medical Sciences Peds Pediatrics, College of Medicine Institutional directory
-
Assistant Professor 2019–2025University of Arkansas for Medical Sciences Department of Pediatrics/Hematology-Oncology Section ORCID
Selected Publications
-
Correction: Exploring Predictive Risk Factors for Myocardial Injury in Children Treated with Anthracyclines: A Pilot Study (2026)
-
Cancer-associated fibroblasts promote tumor progression in fusion-positive rhabdomyosarcoma (2025)
-
Exploring Predictive Risk Factors for Myocardial Injury in Children Treated with Anthracyclines: A Pilot Study (2025)
-
Clinical features and outcomes of young patients with low‐grade non‐rhabdomyosarcoma soft tissue sarcomas treated with a risk‐based strategy: A report from Children's Oncology Group study ARST0332 (2024)
-
Development and validation of a 21-gene prognostic signature in neuroblastoma (2023)
-
Abstract 1558: Targeting CDK9 via the small-molecule inhibitor enitociclib as a therapeutic strategy to treat MYCN-amplified rhabdomyosarcoma and neuroblastoma in children (2023)
-
Neonatal osteoblastic tumor with a novel PTBP1::FOSB fusion (2023)
-
The Role of Pharmacotherapeutic Agents in Children with Desmoid Tumors (2022)
-
A Novel Germline TP53 Mutation in a Patient With Li-Fraumeni Syndrome: Resolving a Variant of Uncertain Significance (2021)
-
A NOVEL GERMLINE TP53 MUTATION IN A PATIENT WITH LI-FRAUMENI SYNDROME - RESOLVING A VARIANT OF UNCERTAIN SIGNIFICANCE (2020)
-
Primary superficial Ewing sarcoma: A unique entity? A case report including novel findings of ELF3 and TNFRSF14 copy number loss (2020)
Collaboration Network
Top Collaborators
- A Novel Germline TP53 Mutation in a Patient With Li-Fraumeni Syndrome: Resolving a Variant of Uncertain Significance
- A NOVEL GERMLINE TP53 MUTATION IN A PATIENT WITH LI-FRAUMENI SYNDROME - RESOLVING A VARIANT OF UNCERTAIN SIGNIFICANCE
- Exploring Predictive Risk Factors for Myocardial Injury in Children Treated with Anthracyclines: A Pilot Study
- Development and validation of a 21-gene prognostic signature in neuroblastoma
- Abstract 1558: Targeting CDK9 via the small-molecule inhibitor enitociclib as a therapeutic strategy to treat MYCN-amplified rhabdomyosarcoma and neuroblastoma in children
- Cancer-associated fibroblasts promote tumor progression in fusion-positive rhabdomyosarcoma
- A Novel Germline TP53 Mutation in a Patient With Li-Fraumeni Syndrome: Resolving a Variant of Uncertain Significance
- A NOVEL GERMLINE TP53 MUTATION IN A PATIENT WITH LI-FRAUMENI SYNDROME - RESOLVING A VARIANT OF UNCERTAIN SIGNIFICANCE
- The Role of Pharmacotherapeutic Agents in Children with Desmoid Tumors
- Clinical features and outcomes of young patients with low‐grade non‐rhabdomyosarcoma soft tissue sarcomas treated with a risk‐based strategy: A report from Children's Oncology Group study ARST0332
- Abstract 1558: Targeting CDK9 via the small-molecule inhibitor enitociclib as a therapeutic strategy to treat MYCN-amplified rhabdomyosarcoma and neuroblastoma in children
- Cancer-associated fibroblasts promote tumor progression in fusion-positive rhabdomyosarcoma
- Abstract 1558: Targeting CDK9 via the small-molecule inhibitor enitociclib as a therapeutic strategy to treat MYCN-amplified rhabdomyosarcoma and neuroblastoma in children
- Cancer-associated fibroblasts promote tumor progression in fusion-positive rhabdomyosarcoma
- Abstract 1558: Targeting CDK9 via the small-molecule inhibitor enitociclib as a therapeutic strategy to treat MYCN-amplified rhabdomyosarcoma and neuroblastoma in children
- Cancer-associated fibroblasts promote tumor progression in fusion-positive rhabdomyosarcoma
- Exploring Predictive Risk Factors for Myocardial Injury in Children Treated with Anthracyclines: A Pilot Study
- Correction: Exploring Predictive Risk Factors for Myocardial Injury in Children Treated with Anthracyclines: A Pilot Study
- Exploring Predictive Risk Factors for Myocardial Injury in Children Treated with Anthracyclines: A Pilot Study
- Correction: Exploring Predictive Risk Factors for Myocardial Injury in Children Treated with Anthracyclines: A Pilot Study
- Exploring Predictive Risk Factors for Myocardial Injury in Children Treated with Anthracyclines: A Pilot Study
- Correction: Exploring Predictive Risk Factors for Myocardial Injury in Children Treated with Anthracyclines: A Pilot Study
- Exploring Predictive Risk Factors for Myocardial Injury in Children Treated with Anthracyclines: A Pilot Study
- Correction: Exploring Predictive Risk Factors for Myocardial Injury in Children Treated with Anthracyclines: A Pilot Study
- Exploring Predictive Risk Factors for Myocardial Injury in Children Treated with Anthracyclines: A Pilot Study
- Correction: Exploring Predictive Risk Factors for Myocardial Injury in Children Treated with Anthracyclines: A Pilot Study
- Primary superficial Ewing sarcoma: A unique entity? A case report including novel findings of ELF3 and TNFRSF14 copy number loss
- Primary superficial Ewing sarcoma: A unique entity? A case report including novel findings of ELF3 and TNFRSF14 copy number loss
- Primary superficial Ewing sarcoma: A unique entity? A case report including novel findings of ELF3 and TNFRSF14 copy number loss
Similar Researchers
Based on overlapping research topics