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Immunohistochemical Expression of FXR1 in Canine Normal Tissues and Melanomas.

Laura NordioAndreia T MarquesCristina LecchiAlberto M LucianoDamiano StefanelloChiara Giudice
Published in: The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society (2018)
Fragile X mental retardation-related protein 1 (FXR1) is a cytoplasmic RNA-binding protein highly conserved among vertebrates. It has been studied for its role in muscle development, inflammation, and tumorigenesis, being related, for example, to metastasizing behavior in human and canine uveal melanoma. Anti-FXR1 antibodies have never been validated in the canine species. To investigate FXR1 expression in canine melanocytic tumors, the present study tested two commercially available polyclonal anti-human FXR1 antibodies, raised in goat and rabbit, respectively. The cross-reactivity of the anti-FXR1 antibodies was assessed by Western blot analysis, and the protein was localized by IHC in a set of normal canine tissues and in canine melanocytic tumors (10 uveal and 10 oral). Western blot results demonstrated that the antibody raised in rabbit specifically recognized the canine FXR1, while the antibody raised in goat did not cross-react with this canine protein. FXR1 protein was immunodetected using rabbit anti-FXR1 antibody, in canine normal tissues with different levels of intensity and distribution. It was also detected in 10/10 uveal and 9/10 oral melanocytic tumors. The present study validated for the first time the use of anti-FXR1 antibody in dogs and highlighted different FXR1 protein expression in canine melanocytic tumors, the significance of which is undergoing further investigations.
Keyphrases
  • binding protein
  • endothelial cells
  • poor prognosis
  • gene expression
  • oxidative stress
  • mental health
  • south africa
  • skeletal muscle
  • long non coding rna
  • protein protein
  • genetic diversity
  • drug induced
  • skin cancer