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Effect of PTFGRN Expression on the Proteomic Profile of A431 Cells and Determination of the PTGFRN Interactome.
Marquez, Jorge; Weldemariam, Mehari M; Dong, Jianping; Hayashi, Jun; Kane, Maureen A; Serrero, Ginette.
Afiliação
  • Marquez J; Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, Maryland 21201, United States of America.
  • Weldemariam MM; Target Discovery Division, A&G Pharmaceutical, Inc., Columbia, Maryland 21045, United States of America.
  • Dong J; Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, Maryland 21201, United States of America.
  • Hayashi J; Target Discovery Division, A&G Pharmaceutical, Inc., Columbia, Maryland 21045, United States of America.
  • Kane MA; Precision Antibody Service, 9130 Red Branch Rd., Suite X Columbia, Maryland 21045, United States.
  • Serrero G; Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, Maryland 21201, United States of America.
ACS Omega ; 9(12): 14381-14387, 2024 Mar 26.
Article em En | MEDLINE | ID: mdl-38559916
ABSTRACT
Prostaglandin F2 receptor negative regulator (PTGFRN) is a transmembrane protein whose expression has been previously implicated in cancer metastasis. However, the exact molecular mechanisms by which PTGFRN influences cancer progression are still unknown. As such, our laboratory set out to investigate how PTGFRN knockdown affected the expression of other proteins. We also carried out coimmunoprecipitation experiments using a monoclonal anti-PTGFRN antibody. We employed mass spectrometry-based proteomics for both experiments to identify proteins that were associated with PTGFRN. Our data show that PTGFRN knockdown increased pathways related to innate immune responses and decreased pathways associated with the synthesis of metabolic precursors and protein processing, among others. Additionally, the coimmunoprecipitation experiments indicated that PTGFRN is associated with proteins involved in processing and metabolism, as well as VEGF signaling molecules. These results highlight the role of PTGFRN as a protein processing regulator, which may be influencing cancer progression.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article