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Disease Subtype-Independent Biomarkers of Breast Cancer Chemoprevention by the Ayurvedic Medicine Phytochemical Withaferin A.
Samanta, Suman K; Sehrawat, Anuradha; Kim, Su-Hyeong; Hahm, Eun-Ryeong; Shuai, Yongli; Roy, Ruchi; Pore, Subrata K; Singh, Krishna B; Christner, Susan M; Beumer, Jan H; Davidson, Nancy E; Singh, Shivendra V.
Afiliación
  • Samanta SK; Department of Pharmacology and Chemical Biology.
  • Sehrawat A; Department of Pharmacology and Chemical Biology.
  • Kim SH; Department of Pharmacology and Chemical Biology.
  • Hahm ER; Department of Pharmacology and Chemical Biology.
  • Shuai Y; Department of Biostatistics.
  • Roy R; University of Pittsburgh Cancer Institute.
  • Pore SK; Department of Pharmacology and Chemical Biology.
  • Singh KB; Department of Pharmacology and Chemical Biology.
  • Christner SM; Department of Pharmacology and Chemical Biology.
  • Beumer JH; University of Pittsburgh Cancer Institute.
  • Davidson NE; University of Pittsburgh Cancer Institute.
  • Singh SV; Department of Pharmaceutical Sciences, University of Pittsburgh School of Medicine, Pittsburgh, PA.
J Natl Cancer Inst ; 109(6)2017 06.
Article en En | MEDLINE | ID: mdl-28040797
Background: A nontoxic chemopreventive intervention efficacious against different subtypes of breast cancer is still a clinically unmet need. The present study was undertaken to determine the efficacy of an Ayurvedic medicine phytochemical (Withaferin A, [WA]) for chemoprevention of breast cancer and to elucidate its mode of action. Methods: Chemopreventive efficacy of WA (4 and 8 mg/kg body weight) was determined using a rat model of breast cancer induced by N-methyl-N-nitrosourea (MNU; n = 14 for control group, n = 15 for 4 mg/kg group, and n = 18 for 8 mg/kg group). The mechanisms underlying breast cancer chemoprevention by WA were elucidated by immunoblotting, biochemical assays, immunohistochemistry, and cytokine profiling using plasma and tumors from the MNU-rat (n = 8-12 for control group, n = 7-11 for 4 mg/kg group, and n = 8-12 for 8 mg/kg group) and/or mouse mammary tumor virus-neu (MMTV-neu) models (n = 4-11 for control group and n = 4-21 for 4 mg/kg group). Inhibitory effect of WA on exit from mitosis and leptin-induced oncogenic signaling was determined using MCF-7 and/or MDA-MB-231 cells. All statistical tests were two-sided. Results: Incidence, multiplicity, and burden of breast cancer in rats were decreased by WA administration. For example, the tumor weight in the 8 mg/kg group was lower by about 68% compared with controls (8 mg/kg vs control, mean = 2.76 vs 8.59, difference = -5.83, 95% confidence interval of difference = -9.89 to -1.76, P = .004). Mitotic arrest and apoptosis induction were some common determinants of breast cancer chemoprevention by WA in the MNU-rat and MMTV-neu models. Cytokine profiling showed suppression of plasma leptin levels by WA in rats. WA inhibited leptin-induced oncogenic signaling in cultured breast cancer cells. Conclusions: WA is a promising chemopreventative phytochemical with the ability to inhibit at least two different subtypes of breast cancer.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Infecciones Tumorales por Virus / Neoplasias de la Mama / Virus del Tumor Mamario del Ratón / Infecciones por Retroviridae / Witanólidos / Neoplasias Mamarias Experimentales Tipo de estudio: Prognostic_studies Idioma: En Revista: J Natl Cancer Inst Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Infecciones Tumorales por Virus / Neoplasias de la Mama / Virus del Tumor Mamario del Ratón / Infecciones por Retroviridae / Witanólidos / Neoplasias Mamarias Experimentales Tipo de estudio: Prognostic_studies Idioma: En Revista: J Natl Cancer Inst Año: 2017 Tipo del documento: Article