skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Inhibition of cell proliferation, migration and invasion of B16-F10 melanoma cells by α-mangostin

Abstract

Highlights: • We studied the anticancer potential of a new emerging molecule, α-mangostin (α-M). • We provide first evidences on the effects of α-M on transglutaminase activity. • We deeply examined the antimetastatic effects of α-M through many in vitro assays. • Proteomic analysis revealed that α-M promotes a reorganization at cellular level. - Abstract: In this study, we have evaluated the potential antineoplastic effects of α-mangostin (α-M), the most representative xanthone in Garcinia mangostana pericarp, on melanoma cell lines. This xanthone markedly inhibits the proliferation of high-metastatic B16-F10 melanoma cells. Furthermore, by deeply analyzing which steps in the metastatic process are influenced by xanthone it was observed that α-M strongly interferes with homotypic aggregation, adhesion, plasticity and invasion ability of B16-F10 cells, probably by the observed reduction of metalloproteinase-9 activity. The antiproliferative and antimetastatic properties of α-M have been established in human SK-MEL-28 and A375 melanoma cells. In order to identify pathways potentially involved in the antineoplastic properties of α-M, a comparative mass spectrometry proteomic approach was employed. These findings may improve our understanding of the molecular mechanisms underlying the anti-cancer effects of α-M on melanoma.

Authors:
 [1];  [1];  [2]; ;  [3]; ; ;  [1];  [1];  [4]
  1. Department of Biology, University “Tor Vergata”, Rome (Italy)
  2. Department of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome (Italy)
  3. Regina Elena National Cancer Institute, Rome (Italy)
  4. (Italy)
Publication Date:
OSTI Identifier:
22416694
Resource Type:
Journal Article
Resource Relation:
Journal Name: Biochemical and Biophysical Research Communications; Journal Volume: 450; Journal Issue: 4; Other Information: Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)
Country of Publication:
United States
Language:
English
Subject:
60 APPLIED LIFE SCIENCES; ADHESION; AGGLOMERATION; CELL PROLIFERATION; DRUGS; HUMAN POPULATIONS; IN VITRO; INHIBITION; MASS SPECTROSCOPY; MELANOMAS; METASTASES; MOLECULES; REDUCTION; TUMOR CELLS

Citation Formats

Beninati, Simone, E-mail: beninati@bio.uniroma2.it, Oliverio, Serafina, Cordella, Martina, Rossi, Stefania, Senatore, Cinzia, Liguori, Immacolata, Lentini, Alessandro, Piredda, Lucia, Tabolacci, Claudio, and Department of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome. Inhibition of cell proliferation, migration and invasion of B16-F10 melanoma cells by α-mangostin. United States: N. p., 2014. Web. doi:10.1016/J.BBRC.2014.07.031.
Beninati, Simone, E-mail: beninati@bio.uniroma2.it, Oliverio, Serafina, Cordella, Martina, Rossi, Stefania, Senatore, Cinzia, Liguori, Immacolata, Lentini, Alessandro, Piredda, Lucia, Tabolacci, Claudio, & Department of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome. Inhibition of cell proliferation, migration and invasion of B16-F10 melanoma cells by α-mangostin. United States. doi:10.1016/J.BBRC.2014.07.031.
Beninati, Simone, E-mail: beninati@bio.uniroma2.it, Oliverio, Serafina, Cordella, Martina, Rossi, Stefania, Senatore, Cinzia, Liguori, Immacolata, Lentini, Alessandro, Piredda, Lucia, Tabolacci, Claudio, and Department of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome. Fri . "Inhibition of cell proliferation, migration and invasion of B16-F10 melanoma cells by α-mangostin". United States. doi:10.1016/J.BBRC.2014.07.031.
@article{osti_22416694,
title = {Inhibition of cell proliferation, migration and invasion of B16-F10 melanoma cells by α-mangostin},
author = {Beninati, Simone, E-mail: beninati@bio.uniroma2.it and Oliverio, Serafina and Cordella, Martina and Rossi, Stefania and Senatore, Cinzia and Liguori, Immacolata and Lentini, Alessandro and Piredda, Lucia and Tabolacci, Claudio and Department of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome},
abstractNote = {Highlights: • We studied the anticancer potential of a new emerging molecule, α-mangostin (α-M). • We provide first evidences on the effects of α-M on transglutaminase activity. • We deeply examined the antimetastatic effects of α-M through many in vitro assays. • Proteomic analysis revealed that α-M promotes a reorganization at cellular level. - Abstract: In this study, we have evaluated the potential antineoplastic effects of α-mangostin (α-M), the most representative xanthone in Garcinia mangostana pericarp, on melanoma cell lines. This xanthone markedly inhibits the proliferation of high-metastatic B16-F10 melanoma cells. Furthermore, by deeply analyzing which steps in the metastatic process are influenced by xanthone it was observed that α-M strongly interferes with homotypic aggregation, adhesion, plasticity and invasion ability of B16-F10 cells, probably by the observed reduction of metalloproteinase-9 activity. The antiproliferative and antimetastatic properties of α-M have been established in human SK-MEL-28 and A375 melanoma cells. In order to identify pathways potentially involved in the antineoplastic properties of α-M, a comparative mass spectrometry proteomic approach was employed. These findings may improve our understanding of the molecular mechanisms underlying the anti-cancer effects of α-M on melanoma.},
doi = {10.1016/J.BBRC.2014.07.031},
journal = {Biochemical and Biophysical Research Communications},
number = 4,
volume = 450,
place = {United States},
year = {Fri Aug 08 00:00:00 EDT 2014},
month = {Fri Aug 08 00:00:00 EDT 2014}
}