Newsletters
TOLLIP Inhibits Psoriasis Progression via Suppressing PKM2-Mediated Glycolysis in Keratinocytes
[Advanced Science] Investigators identify Toll-interacting protein (TOLLIP) as a critical regulator of psoriasis pathogenesis through its modulation of glycolytic metabolism.
Failed Metabolic Adaptation to Stress Contributes to Epidermal Cell Adhesion Defects in Darier Disease
[Science Advances] Researchers explored how extra-genetic factors, particularly metabolic and oxidative stress, influence Darier disease, showing that impaired antioxidant defenses can compromise SERCA2 function and weaken epidermal cell adhesion.
Fibroblasts Resist Staphylococcus aureus on the Skin Surface by Responding to Interleukin-1 and Recruiting Neutrophils
[Science Advances] Using unbiased transcriptomic, biochemical, and phosphoproteomic analyses, followed by targeted validation in human and mouse models, investigators found that fibroblast recognition of interleukin-1 is essential for immune response.
Screening Cross-Injury Responses in Skin Organoids Identifies a THBS2-Enriched Pro-Repair Fibroblast State during Regeneration
[Journal of Advanced Research] Scientists established a high-fidelity mouse skin organoid platform to simulate clinically relevant stressors and identify the core regulatory components of the regenerative program.
MICAL2 As a Key Effector of β-catenin Signaling Driving Melanoma Progression and Therapeutic Resistance
[Cell Death & Differentiation] The authors demonstrate that activation of β-catenin is associated with a poor prognosis in melanoma. This conclusion was based on immunohistochemical analysis of a cohort of 157 patients and the identification of a genetic signature for melanoma upon β-catenin activation.
Metabolism Alterations Accompany the Invasive Phenotype of Melanoma Cells Resistant to BRAF/MEK Inhibitors
[Biochimica Et Biophysica Acta-Molecular Cell Research] Researchers showed that melanoma cells resistant to BRAF (B-raf serine-threonine-protein kinase)/MEK (mitogen-activated protein kinase kinase)inhibitors undergo metabolic rewiring that supports a more invasive phenotype, linking therapy resistance with altered glycolysis, mitochondrial function, and lipid metabolism.
Ferroptosis in Vitiligo and Melanoma: Opposing Susceptibilities, Shared Mechanisms, and Therapeutic Targets
[Experimental Cell Research] Scientists highlight the contrasting roles of ferroptosis in vitiligo and melanoma, revealing shared mechanisms that could be exploited for melanocyte-specific therapeutic strategies.
UBC Medicine Researchers Awarded More Than $39 Million in CIHR Funding
[The University of British Columbia] UBC Faculty of Medicine researchers have been awarded more than $39 million in federal funding through the Canadian Institutes of Health Research (CIHR) Project Grant: Spring 2026 competition.
Lupus Foundation of America Awards Grants to Early Career Scientists Advancing Understanding of Lupus and Targeted Treatment Pathways
[Lupus Foundation of America] The Lupus Foundation of America announced the recipients of the 2026 Gary S. Gilkeson Career Development Award. The two-year grant supports early career scientists at a pivotal time in their professions, providing funding for critical research studies and mentorship to foster the growth of the lupus research field.
UV Irradiation Drives Lineage-Specific MITF-Mediated Transcription of PD-L1 to Confer Immune Tolerance to UV-Mutated Melanocytes
[Immunity] Researchers investigated whether melanocyte-intrinsic transcriptional program(s) underlie immune tolerance to mutations resulting from UV radiation exposure.
Metabolic-Epigenetic Crosstalk in Innate Immune Cell Plasticity Within the Tumor Microenvironment
[Experimental & Molecular Medicine] Emerging evidence highlights the intricate interplay between metabolic reprogramming and epigenetic modifications in macrophages, neutrophils, and other innate immune populations within the tumor microenvironment.
A Regulatory T Cell-Biased IL-2 Mutein Inhibits the Development of Allergen-Specific Th2 Cells and Allergic Asthma
[Journal of Allergy and Clinical Immunology] Investigators explored the effects of the IL-2 mutein Fc.mut24 on allergen-induced type 2 airway inflammation. Fc.mut24 therapy prevented allergic airway inflammation when delivered before type 2 effector T cell priming but was insufficient to overcome established allergen-specific type 2 responses.

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