Biology subjects

Safi, S.

Publications and source records attributed to Safi, S..

3 recordsLinked to original sources

bioRxiv2026

Discrete Pain Behavior Without Systemic Inflammation in a Rat Osteotomy Model: A Platform for Analgesic Screening

BackgroundThis study aimed to determine if a rat osteotomy model elicits a measurable systemic response and to utilize this profile to evaluate the mechanism of action of preemptive analgesics with translational relevance to veterinary perioperative pain management. MethodsTwenty-five male rats were randomized into five groups: Sham, Surgery Control, Robenacoxib (2 mg/kg S.C.), Amantadine (30 mg/kg P.O.), and Combination. A femoral osteotomy was performed following ARRIVE 2.0 guidelines for refinement of surgical models. Serum levels of IL-6, PGE2, and cortisol were quantified via ELISA at baseline, 1-, 3-, and 6- hours post-surgery. Postoperative pain was assessed using the Rat Grimace Scale (RGS). ResultsThe osteotomy model did not induce a significant systemic inflammatory or stress response. Serum IL-6 and cortisol levels showed no significant changes over time (IL-6: p=0.219; Cortisol: p=0.187) or between groups. While PGE2 showed a temporal increase (F=6.52, p=0.001), it was unaffected by drug treatments. In stark contrast, the model successfully produced significant pain-related behaviors in the Control group (p=0.007), which were effectively reduced by both Robenacoxib (p=0.014) and amantadine (p=0.019) monotherapies. The combination group also showed significant pain reduction compared to Control at T6 (p=0.002), with an additive effect relative to monotherapies. Correlation analysis confirmed a dissociation between systemic biomarker levels and pain scores. ConclusionThe efficacy of Robenacoxib (a COX-2 inhibitor approved for veterinary use) and amantadine in the absence of altered systemic biomarkers suggests their analgesic actions are mediated predominantly through local or neurogenic pathways, with direct implications for optimizing perioperative analgesia protocols in companion animal orthopedic surgery.

neuroscience↗

bioRxiv2026

GALE-dependent glycoproteome remodelling is a determinant of oncogenic RAS transformation

Oncogenic transformation is accompanied by extensive remodelling of the cellular glycosylation landscape, yet the mechanisms linking oncogenic signalling to glycoproteome reprogramming remain poorly defined. We used site-resolved intact glycoproteomics to systematically map oncogenic RAS-dependent changes across the N- and O-linked glycoproteome. Integrating multiomics profiling with functional approaches, we identify UDP-glucose 4-epimerase (GALE) as a transcriptional target of oncogenic RAS that is induced through MAPK signalling and MYC-dependent transcription. GALE depletion selectively disrupted RAS-dependent glycoproteome remodelling, preferentially impairing sialylation of N-linked glycans and O-linked GalNAc-type glycosylation. Functionally, these glycosylation defects were accompanied by suppressed anchorage-independent growth and reduced in vivo tumorigenicity of KRAS-mutant cells, establishing GALE-dependent nucleotide-sugar interconversion as a requirement for malignant growth. Clinically, GALE expression was elevated in pancreatic ductal adenocarcinoma, wherein KRAS mutations are highly prevalent, and across a broad spectrum of human cancers. Collectively, our findings define a regulatory axis that connects oncogenic signalling to nucleotide-sugar precursor availability and diversification of the cellular glycan repertoire, revealing GALE as a metabolic dependency in RAS-driven cancer.

Cancer Biology↗

bioRxiv2025

Quantification of Wnt3a, Wnt5a and Wnt16 Binding to Multiple Frizzleds Under Physiological Conditions using NanoBit/BRET

Upon engagement of one of the 19 secreted Wnt signalling proteins with one of the 10 Frizzled transmembrane Wnt receptors (FZD1-10), a wide variety of cellular Wnt signalling responses can be elicited, the selectivity of which depends on: 1) the specific Wnt-FZD pairing, 2) the participation of Wnt co-receptors, and 3) the cellular context. Co-receptors play a pivotal role in guiding the specificity of Wnt signaling, most notably between {beta}-catenin dependent and independent pathways, where co-receptors such as LRP5/6 and ROR1/2 / PTK7 play major roles, respectively. It remains less understood how specific Wnt/FZD combinations contribute to the selectivity of downstream Wnt signaling and we lack accurate comparative data on their binding properties under physiological conditions. Here, using fluorescently-tagged Wnt3a, Wnt5a and Wnt16 proteins and cell lines expressing HiBiT-tagged Frizzled, we build on our ongoing efforts to provide a complete overview of the biophysical properties of all Wnt/FZD interactions using full-length proteins. Our real-time NanoBRET analysis using living cells expressing low receptor levels provides more accurate quantification of binding and will help us understand how these binary engagements control Wnt signaling outputs. We also provide evidence that LRP6 regulates the binding affinity of Wnt/FZD interactions in the trimeric Wnt-FZD-LRP6 complex.

biochemistry↗