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Pre-clinical evaluation of small molecule LOXL2 inhibitors in breast cancer.
Chang, Joan; Lucas, Morghan C; Leonte, Lidia E; Garcia-Montolio, Marc; Singh, Lukram Babloo; Findlay, Alison D; Deodhar, Mandar; Foot, Jonathan S; Jarolimek, Wolfgang; Timpson, Paul; Erler, Janine T; Cox, Thomas R.
Afiliação
  • Chang J; Biotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Copenhagen, Denmark.
  • Lucas MC; The Garvan Institute of Medical Research and The Kinghorn Cancer Centre, Cancer Division, St Vincent's Clinical School, Faculty of Medicine, University of New South Wales, Sydney, Australia.
  • Leonte LE; Biotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Copenhagen, Denmark.
  • Garcia-Montolio M; Biotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Copenhagen, Denmark.
  • Singh LB; Biotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Copenhagen, Denmark.
  • Findlay AD; Pharmaxis Pharmaceutical Ltd., Frenchs Forest, Australia.
  • Deodhar M; Pharmaxis Pharmaceutical Ltd., Frenchs Forest, Australia.
  • Foot JS; Pharmaxis Pharmaceutical Ltd., Frenchs Forest, Australia.
  • Jarolimek W; Pharmaxis Pharmaceutical Ltd., Frenchs Forest, Australia.
  • Timpson P; The Garvan Institute of Medical Research and The Kinghorn Cancer Centre, Cancer Division, St Vincent's Clinical School, Faculty of Medicine, University of New South Wales, Sydney, Australia.
  • Erler JT; Biotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Copenhagen, Denmark.
  • Cox TR; Biotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Copenhagen, Denmark.
Oncotarget ; 8(16): 26066-26078, 2017 Apr 18.
Article em En | MEDLINE | ID: mdl-28199967
ABSTRACT
Lysyl Oxidase-like 2 (LOXL2), a member of the lysyl oxidase family of amine oxidases is known to be important in normal tissue development and homeostasis, as well as the onset and progression of solid tumors. Here we tested the anti-tumor properties of two generations of novel small molecule LOXL2 inhibitor in the MDA-MB-231 human model of breast cancer. We confirmed a functional role for LOXL2 activity in the progression of primary breast cancer. Inhibition of LOXL2 activity inhibited the growth of primary tumors and reduced primary tumor angiogenesis. Dual inhibition of LOXL2 and LOX showed a greater effect and also led to a lower overall metastatic burden in the lung and liver. Our data provides the first evidence to support a role for LOXL2 specific small molecule inhibitors as a potential therapy in breast cancer.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Inibidores Enzimáticos / Aminoácido Oxirredutases / Antineoplásicos Limite: Animals / Female / Humans Idioma: En Revista: Oncotarget Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Dinamarca

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Inibidores Enzimáticos / Aminoácido Oxirredutases / Antineoplásicos Limite: Animals / Female / Humans Idioma: En Revista: Oncotarget Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Dinamarca