Your browser doesn't support javascript.
loading
A catechin nanoformulation inhibits WM266 melanoma cell proliferation, migration and associated neo-angiogenesis.
di Leo, Nicoletta; Battaglini, Matteo; Berger, Liron; Giannaccini, Martina; Dente, Luciana; Hampel, Silke; Vittorio, Orazio; Cirillo, Giuseppe; Raffa, Vittoria.
Affiliation
  • di Leo N; Department of Biology, Università di Pisa, Pisa 56127, Italy.
  • Battaglini M; Department of Biology, Università di Pisa, Pisa 56127, Italy.
  • Berger L; Istituto di Scienze della Vita, Scuola Superiore Sant'Anna, 56127, Italy.
  • Giannaccini M; Department of Biology, Università di Pisa, Pisa 56127, Italy.
  • Dente L; Department of Biology, Università di Pisa, Pisa 56127, Italy; Interdepartmental Research Centre "Nutraceuticals and Food for Health", Università di Pisa, Pisa 56124, Italy.
  • Hampel S; Leibniz Institute for Solid State and Materials Research Dresden, Dresden D-01171, Germany.
  • Vittorio O; Children's Cancer Institute Australia, Lowy Cancer Research Centre, UNSW Australia, Sydney 2031, Australia; Australian Centre for NanoMedicine, UNSW Australia, Sydney 2031, Australia.
  • Cirillo G; Department of Pharmacy, Health and Nutritional Sciences, Università degli Studi di Calabria, Rende, CS 87036, Italy.
  • Raffa V; Department of Biology, Università di Pisa, Pisa 56127, Italy; Istituto di Scienze della Vita, Scuola Superiore Sant'Anna, 56127, Italy; IMSaT, University of Dundee, DD2 1FD, United Kingdom. Electronic address: vittoria.raffa@unipi.it.
Eur J Pharm Biopharm ; 114: 1-10, 2017 May.
Article in En | MEDLINE | ID: mdl-28088004
We validated the anticancer potential of a nanoformulation made by (+)-catechin, gelatin and carbon nanotubes in terms of inhibition of cancer cell proliferation, migration and associated neo-angiogenesis. Gelatin was selected to stabilize the catechin without compromising its anti-oxidant potential and the carbon nanotubes were used to increase its intracellular bioavailability. The anticancer potential of the resulting nanohybrid was validated on an aggressive melanoma cell line, in vitro and in zebrafish xenotransplants. The nanohybrid strongly enhances the cytotoxic effect of (+)-catechin. At a concentration of (+)-catechin 50µg/ml, the nanohybrid inhibited the ability of melanoma cells to proliferate (100% increase of cell doubling time and severe impairment in zebrafish xenotransplants), to migrate (totally inhibition in vitro and 50% reduction of cell motility in zebrafish xenotransplants) and to induce neo-angiogenesis (100% inhibition in zebrafish xenotransplants). Conversely, the free (+)-catechin and carrier (CNT:gel) had no statistically significant effects over the control, at any concentration tested. Our results suggest that the use of the nanohybrid, able to improve the therapeutic efficacy of the catechins, could represent a successful strategy for a future clinical translation.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Catechin / Angiogenesis Inhibitors / Cell Proliferation / Melanoma / Antineoplastic Agents, Phytogenic Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals / Humans Language: En Journal: Eur J Pharm Biopharm Journal subject: FARMACIA / FARMACOLOGIA Year: 2017 Document type: Article Affiliation country: Italy Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Catechin / Angiogenesis Inhibitors / Cell Proliferation / Melanoma / Antineoplastic Agents, Phytogenic Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals / Humans Language: En Journal: Eur J Pharm Biopharm Journal subject: FARMACIA / FARMACOLOGIA Year: 2017 Document type: Article Affiliation country: Italy Country of publication: Netherlands