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Application of small molecule FPR1 antagonists in the treatment of cancers.
Ahmet, Djevdet S; Basheer, Haneen A; Salem, Anwar; Lu, Di; Aghamohammadi, Amin; Weyerhäuser, Patrick; Bordiga, Andrea; Almeniawi, Juman; Rashid, Sabah; Cooper, Patricia A; Shnyder, Steven D; Vinader, Victoria; Afarinkia, Kamyar.
Afiliação
  • Ahmet DS; Institute of Cancer Therapeutics, University of Bradford, Richmond Road, Bradford, BD7 1DP, UK.
  • Basheer HA; Faculty of Pharmacy, Zarqa University, PO Box 132222, Zarqa, 13132, Jordan.
  • Salem A; Institute of Cancer Therapeutics, University of Bradford, Richmond Road, Bradford, BD7 1DP, UK.
  • Lu D; Institute of Cancer Therapeutics, University of Bradford, Richmond Road, Bradford, BD7 1DP, UK.
  • Aghamohammadi A; Institute of Cancer Therapeutics, University of Bradford, Richmond Road, Bradford, BD7 1DP, UK.
  • Weyerhäuser P; Institut für Toxikologie, Universitätsmedizin Mainz, Gebäude 905/4. OG, Obere Zahlbacher Str. 67, 55131, Mainz, Germany.
  • Bordiga A; Dipartimento di Scienza e Tecnologia del Farmaco, Universitá Degli Studi di Torino, Via P. Giuria 9, 10125, Torino, Italy.
  • Almeniawi J; Institute of Cancer Therapeutics, University of Bradford, Richmond Road, Bradford, BD7 1DP, UK.
  • Rashid S; Institute of Cancer Therapeutics, University of Bradford, Richmond Road, Bradford, BD7 1DP, UK.
  • Cooper PA; Institute of Cancer Therapeutics, University of Bradford, Richmond Road, Bradford, BD7 1DP, UK.
  • Shnyder SD; Institute of Cancer Therapeutics, University of Bradford, Richmond Road, Bradford, BD7 1DP, UK.
  • Vinader V; Institute of Cancer Therapeutics, University of Bradford, Richmond Road, Bradford, BD7 1DP, UK.
  • Afarinkia K; Institute of Cancer Therapeutics, University of Bradford, Richmond Road, Bradford, BD7 1DP, UK. k.afarinkia@bradford.ac.uk.
Sci Rep ; 10(1): 17249, 2020 10 14.
Article em En | MEDLINE | ID: mdl-33057069
ABSTRACT
The formylpeptide receptor-1 (FPR1) is a member of the chemotactic GPCR-7TM formyl peptide receptor family, whose principle function is in trafficking of various leukocytes into sites of bacterial infection and inflammation. More recently, FPR1 has been shown to be expressed in different types of cancer and in this context, plays a significant role in their expansion, resistance and recurrence. ICT12035 is a selective and potent (30 nM in calcium mobilisation assay) small molecule FPR1 antagonist. Here, we demonstrate the efficacy of ICT12035, in a number of 2D and 3D proliferation and invasion in vitro assays and an in vivo model. Our results demonstrate that targeting FPR1 by a selective small molecule antagonist, such as ICT12035, can provide a new avenue for the treatment of cancers.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores de Formil Peptídeo / Bibliotecas de Moléculas Pequenas / Neoplasias Limite: Animals / Humans Idioma: En Revista: Sci Rep Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores de Formil Peptídeo / Bibliotecas de Moléculas Pequenas / Neoplasias Limite: Animals / Humans Idioma: En Revista: Sci Rep Ano de publicação: 2020 Tipo de documento: Article