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Selective EGLN Inhibition Enables Ablative Radiotherapy and Improves Survival in Unresectable Pancreatic Cancer.
Fujimoto, Tara N; Colbert, Lauren E; Huang, Yanqing; Molkentine, Jessica M; Deorukhkar, Amit; Baseler, Laura; de la Cruz Bonilla, Marimar; Yu, Meifang; Lin, Daniel; Gupta, Sonal; Cabeceiras, Peter K; Kingsley, Charles V; Tailor, Ramesh C; Sawakuchi, Gabriel O; Koay, Eugene J; Piwnica-Worms, Helen; Maitra, Anirban; Taniguchi, Cullen M.
Afiliação
  • Fujimoto TN; Department of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Colbert LE; Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Huang Y; Department of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Molkentine JM; Department of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Deorukhkar A; Department of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Baseler L; Department of Veterinary Medicine & Surgery, UT MD Anderson Cancer Center, Houston, Texas.
  • de la Cruz Bonilla; Department of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Yu M; Department of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Lin D; Department of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Gupta S; Department of Pathology, UT MD Anderson Cancer Center, Houston, Texas.
  • Cabeceiras PK; Department of Translational Molecular Pathology, UT MD Anderson Cancer Center, Houston, Texas.
  • Kingsley CV; Department of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Tailor RC; Department of Imaging Physics, UT MD Anderson Cancer Center, Houston, Texas.
  • Sawakuchi GO; Department of Radiation Physics, UT MD Anderson Cancer Center, Houston, Texas.
  • Koay EJ; Department of Radiation Physics, UT MD Anderson Cancer Center, Houston, Texas.
  • Piwnica-Worms H; Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Maitra A; Department of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Taniguchi CM; Department of Pathology, UT MD Anderson Cancer Center, Houston, Texas.
Cancer Res ; 79(9): 2327-2338, 2019 05 01.
Article em En | MEDLINE | ID: mdl-31043430
When pancreatic cancer cannot be removed surgically, patients frequently experience morbidity and death from progression of their primary tumor. Radiation therapy (RT) cannot yet substitute for an operation because radiation causes fatal bleeding and ulceration of the nearby stomach and intestines before achieving tumor control. There are no FDA-approved medications that prevent or reduce radiation-induced gastrointestinal injury. Here, we overcome this fundamental problem of anatomy and biology with the use of the oral EGLN inhibitor FG-4592, which selectively protects the intestinal tract from radiation toxicity without protecting tumors. A total of 70 KPC mice with autochthonous pancreatic tumors received oral FG-4592 or vehicle control ± ablative RT to a cumulative 75 Gy administered in 15 daily fractions to a limited tumor field. Although ablative RT reduced complications from local tumor progression, fatal gastrointestinal bleeding was observed in 56% of mice that received high-dose RT with vehicle control. However, radiation-induced bleeding was completely ameliorated in mice that received high-dose RT with FG-4592 (0% bleeding, P < 0.0001 compared with vehicle). Furthermore, FG-4592 reduced epithelial apoptosis by half (P = 0.002) and increased intestinal microvessel density by 80% compared with vehicle controls. EGLN inhibition did not stimulate cancer growth, as treatment with FG-4592 alone, or overexpression of HIF2 within KPC tumors independently improved survival. Thus, we provide a proof of concept for the selective protection of the intestinal tract by the EGLN inhibition to enable ablative doses of cytotoxic therapy in unresectable pancreatic cancer by reducing untoward morbidity and death from radiation-induced gastrointestinal bleeding. SIGNIFICANCE: Selective protection of the intestinal tract by EGLN inhibition enables potentially definitive doses of radiation therapy. This might allow radiation to be a surgical surrogate for unresectable pancreatic cancer.Graphical Abstract: http://cancerres.aacrjournals.org/content/canres/79/9/2327/F1.large.jpg.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Lesões por Radiação / Protetores contra Radiação / Radioterapia / Prolina Dioxigenases do Fator Induzível por Hipóxia / Glicina / Isoquinolinas Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Lesões por Radiação / Protetores contra Radiação / Radioterapia / Prolina Dioxigenases do Fator Induzível por Hipóxia / Glicina / Isoquinolinas Idioma: En Ano de publicação: 2019 Tipo de documento: Article