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Evaluation of Biodistribution of Sulforaphane after Administration of Oral Broccoli Sprout Extract in Melanoma Patients with Multiple Atypical Nevi.
Tahata, Shawn; Singh, Shivendra V; Lin, Yan; Hahm, Eun-Ryeong; Beumer, Jan H; Christner, Susan M; Rao, Uma N; Sander, Cindy; Tarhini, Ahmad A; Tawbi, Hussein; Ferris, Laura K; Wilson, Melissa; Rose, Amy; Dietz, Catherine M; Hughes, Ellen; Fahey, Jed W; Leachman, Sancy A; Cassidy, Pamela B; Butterfield, Lisa H; Zarour, Hassane M; Kirkwood, John M.
Affiliation
  • Tahata S; UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Singh SV; UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Lin Y; Department of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Hahm ER; UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Beumer JH; Department of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Christner SM; UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Rao UN; Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Sander C; Department of Pharmaceutical Sciences, University of Pittsburgh School of Pharmacy, Pittsburgh, Pennsylvania.
  • Tarhini AA; UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Tawbi H; UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Ferris LK; UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Wilson M; Cleveland Clinic Taussig Cancer Institute, Cleveland, Ohio.
  • Rose A; Department of Melanoma Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Dietz CM; Department of Dermatology, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Hughes E; UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Fahey JW; UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Leachman SA; Computer Vision Group, Veytel, LLC, Pittsburgh, Pennsylvania.
  • Cassidy PB; Computer Vision Group, Veytel, LLC, Pittsburgh, Pennsylvania.
  • Butterfield LH; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Zarour HM; Knight Cancer Institute, Oregon Health and Science University, Portland, Oregon.
  • Kirkwood JM; Knight Cancer Institute, Oregon Health and Science University, Portland, Oregon.
Cancer Prev Res (Phila) ; 11(7): 429-438, 2018 07.
Article in En | MEDLINE | ID: mdl-29691233
ABSTRACT
Broccoli sprout extract containing sulforaphane (BSE-SFN) has been shown to inhibit ultraviolet radiation-induced damage and tumor progression in skin. This study evaluated the toxicity and potential effects of oral BSE-SFN at three dosages. Seventeen patients who each had at least 2 atypical nevi and a prior history of melanoma were randomly allocated to 50, 100, or 200 µmol oral BSE-SFN daily for 28 days. Atypical nevi were photographed on days 1 and 28, and plasma and nevus samples were taken on days 1, 2, and 28. Endpoints assessed were safety, plasma and skin sulforaphane levels, gross and histologic changes, IHC for phospho-STAT3(Y705), Ki-67, Bcl-2, HMOX1, and TUNEL, plasma cytokine levels, and tissue proteomics. All 17 patients completed 28 days with no dose-limiting toxicities. Plasma sulforaphane levels pooled for days 1, 2, and 28 showed median postadministration increases of 120 ng/mL for 50 µmol, 206 ng/mL for 100 µmol, and 655 ng/mL for 200 µmol. Median skin sulforaphane levels on day 28 were 0.0, 3.1, and 34.1 ng/g for 50, 100, and 200 µmol, respectively. Plasma levels of proinflammatory cytokines decreased from day 1 to 28. The tumor suppressor decorin was increased from day 1 to 28. Oral BSE-SFN is well tolerated at daily doses up to 200 µmol and achieves dose-dependent levels in plasma and skin. A larger efficacy evaluation of 200 µmol daily for longer intervals is now reasonable to better characterize clinical and biological effects of BSE-SFN as chemoprevention for melanoma. Cancer Prev Res; 11(7); 429-38. ©2018 AACR.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Skin Neoplasms / Brassica / Plant Extracts / Isothiocyanates / Melanoma / Nevus Type of study: Clinical_trials Language: En Journal: Cancer Prev Res (Phila) Year: 2018 Type: Article

Full text: 1 Database: MEDLINE Main subject: Skin Neoplasms / Brassica / Plant Extracts / Isothiocyanates / Melanoma / Nevus Type of study: Clinical_trials Language: En Journal: Cancer Prev Res (Phila) Year: 2018 Type: Article