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QP6126, an Orally Bioavailable QPCTL Inhibitor, with Anti-Tumor Activity in Melanoma Tumor Model
[International Immunopharmacology] Scientists reported the discovery of QP6126, a small-molecule glutaminyl-peptide cyclotransferase-like protein (QPCTL) inhibitor. QP6126 ablates the pGlu-CD47 modification, thereby abolishing CD47-SIRPα interaction, and sensitizing melanoma cells to macrophage-mediated phagocytosis.
Powering Skin Repair: Piezoelectric Biomaterials-Driven Wound Healing
[Advanced Materials] The authors provide an overview of piezoelectric biomaterials for skin wound healing and examine the physiological and biochemical roles of the naturally occurring electric fields in healthy skin and injured skin.
The Skin-Specific Long Non-Coding RNA TEDAR Orchestrates Late Epidermal Differentiation via an ERK-KLF4 Cytoplasmic Regulatory Axis
[Cell Death & Disease] Using transcriptome analysis of more than 15,000 RNA-seq samples across 54 human tissues, scientists identified terminal epidermal differentiation-associated RNA (TEDAR), a highly skin-enriched lncRNA.
ALKBH5 Acts As a Regulator of Hair Follicle Telogen-to-Anagen Transition in Mice
[Communications Biology] Investigators showed that Alkbh5 expression is downregulated during late telogen, and its deletion promotes hair follicle stem cell activation and proliferation, accelerating the telogen–anagen transition in mice.
Type 3 Inflammation-Specific Keratinocyte Glutaminolysis Promotes Skin Inflammation
[JCI Insight] Researchers identified GLS1-mediated glutaminolysis as a metabolic program preferentially induced in keratinocytes under type 3 inflammatory conditions. Integrated transcriptomic, metabolomic, genetic, and functional analyses showed that IL-17A induced GLS1 expression and glutaminolysis in keratinocytes.
α-Ketoglutarate Accelerates Cutaneous Wound Healing through Modulating the Epithelial-Fibroblast Niche
[JCI Insight] Investigators employed multiomics profiling of clinical samples to investigate metabolic alterations during wound healing. They developed a transdermal microneedle platform based on gelatin methacryloyl for localized αKG delivery, further accelerating tissue repair.
Lavender Essential Oil Coordinates Epidermal GABA Shunt and Nucleotide Turnover to Rescue Cortisol-Induced Stress Damage
[Scientific Reports] Researchers established an epidermal stress model was established using cortisol-stimulated human keratinocytes to systematically evaluate the cytoprotective effects of Taikong Blue lavender essential oil .
Immunocore Announces Achievement of Target Enrollment in Registrational TEBE-AM Trial with KIMMTRAK® (Tebentafusp) in Previously Treated Advanced Melanoma
[Immunocore ] Immunocore announced the achievement of target patient enrollment in the TEBE-AM clinical trial, a randomized, registrational Phase III clinical trial evaluating KIMMTRAK as monotherapy and in combination with pembrolizumab for the treatment of HLA-A*02:01-positive patients with advanced melanoma.
Cancer-Driver-Agnostic Targeting of Amplified Surface Proteins Identifies MPZL1 for Selective CAR-T Cell Therapy
[Nature Communications] Researchers developed a monoclonal antibody targeting myelin protein zero–like 1 (MPZL1)’s extracellular domain and engineered CAR-T cells that selectively eliminate MPZL1-positive cancer cells in vitro.
From Cellular Therapy to Biologics: Non-Viral Delivery Strategies for In Vivo CAR-T Engineering
[Critical Reviews in Oncology/Hematology] The authors provide an overview of the key physiological barriers encountered in in vivo CAR-T cell engineering, alongside the corresponding principles of engineered design.
Safety and Efficacy of Allogeneic CD19-Directed CAR-T Therapy CTX110 in Relapsed/Refractory B-Cell Non-Hodgkin Lymphoma
[Blood Advances] This multicenter, single-arm, Phase I/II study evaluated the safety and efficacy of CD19-directed allogeneic CAR immunotherapy CTX110 in adult patients with relapsed/refractory B cell non-Hodgkin lymphoma.
Autologous Glypican-3-Targeted, Armored CAR T Cells in Patients with Advanced Solid Tumors: A Phase 1 Dose-Escalation Study of TAK-102
[Cancer Immunology Research] In this first-in-human, open-label, Phase I, dose-escalation study, researchers evaluated a single TAK-102 infusion in 11 patients with glypican-3-positive advanced solid tumors refractory or intolerant to standard therapies.

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