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Rutin as A Novel c-Met Inhibitory Lead for The Control of Triple Negative Breast Malignancies.
Elsayed, Heba E; Ebrahim, Hassan Y; Mohyeldin, Mohamed M; Siddique, Abu Bakar; Kamal, Amel M; Haggag, Eman G; El Sayed, Khalid A.
Affiliation
  • Elsayed HE; a Department of Basic Pharmaceutical Sciences, School of Pharmacy , University of Louisiana at Monroe , Monroe , Louisiana.
  • Ebrahim HY; b Department of Pharmacognosy, Faculty of Pharmacy , Helwan University , Helwan , Cairo , Egypt.
  • Mohyeldin MM; a Department of Basic Pharmaceutical Sciences, School of Pharmacy , University of Louisiana at Monroe , Monroe , Louisiana.
  • Siddique AB; a Department of Basic Pharmaceutical Sciences, School of Pharmacy , University of Louisiana at Monroe , Monroe , Louisiana.
  • Kamal AM; a Department of Basic Pharmaceutical Sciences, School of Pharmacy , University of Louisiana at Monroe , Monroe , Louisiana.
  • Haggag EG; b Department of Pharmacognosy, Faculty of Pharmacy , Helwan University , Helwan , Cairo , Egypt.
  • El Sayed KA; b Department of Pharmacognosy, Faculty of Pharmacy , Helwan University , Helwan , Cairo , Egypt.
Nutr Cancer ; 69(8): 1256-1271, 2017.
Article in En | MEDLINE | ID: mdl-29083228
ABSTRACT
Triple negative breast cancer (TNBC) has high metastatic and mortality potential and lacks effective and selective therapeutic options. Aberrant dysregulation of the receptor tyrosine kinase c-Met promotes TNBC progression, motility and survival and therefore considered a valid therapeutic target. Among various identified anticancer agents, plant polyphenols (PPs) including flavonoids, have been shown to be safe and proven for their antitumor activity through modulating diverse macromolecular targets. This study reports the bioassay-guided identification of the common flavonol glycoside rutin as breast cancer cell proliferation, migration and invasion inhibitor. The cell free Z'-LYTE kinase assay, Western blot and in silico docking experiments uncovered, for the first time, c-Met kinase as a potential mechanistic target for rutin-mediated anticancer effects on TNBC cell lines. Likewise, the intraperitoneal injection of rutin at 30 mg/kg, 3X/week, significantly reduced the growth of the TNBC MDA-MB-231/GFP orthotopic xenograft in nude mouse model. These results clearly designate the functional dietary flavonoid rutin as a potential lead for the prevention and control of c-Met-dependent breast malignancies.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Rutin / Proto-Oncogene Proteins c-met / Triple Negative Breast Neoplasms / Antineoplastic Agents Type of study: Prognostic_studies Limits: Animals / Female / Humans Language: En Year: 2017 Type: Article

Full text: 1 Database: MEDLINE Main subject: Rutin / Proto-Oncogene Proteins c-met / Triple Negative Breast Neoplasms / Antineoplastic Agents Type of study: Prognostic_studies Limits: Animals / Female / Humans Language: En Year: 2017 Type: Article