Publications by authors named "C Pecqueur"

The CRCINA inaugural symposium, a meeting on tumor and immune ecosystems, took place in the vibrant and picturesque city of Nantes. The meeting gathered world-renowned experts in cancer biology and immunology. It showcased the most advanced science on mechanisms driving cellular heterogeneity, plasticity, and signaling in normal and cancer cellular ecosystems, which contribute to cancer development, progression, and therapeutic resistance.

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Article Synopsis
  • Glioblastoma (GBM) is a very aggressive brain tumor with treatment challenges due to its complex and varying characteristics; this study focuses on the metabolic features of Glioblastoma stem cells (GSC) that are crucial for tumor growth and resistance to therapies.
  • Researchers performed extensive analyses on brain tumor cultures and found that GSCs have unique glycolytic profiles compared to regular tumor cells, heavily relying on the enzyme pyruvate carboxylase (PC) for their survival and growth.
  • Inhibiting PC leads to GSC death, increases differentiation, and can restore sensitivity to the chemotherapy drug etoposide, indicating that targeting PC could be an effective strategy to combat therapy resistance in GBM.
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The advent of novel 2D and 3D models for human development, including trophoblast stem cells and blastoids, has expanded opportunities for investigating early developmental events, gradually illuminating the enigmatic realm of human development. While these innovations have ushered in new prospects, it has become essential to establish well-defined benchmarks for the cell sources of these models. We aimed to propose a comprehensive characterization of pluripotent and trophoblastic stem cell models by employing a combination of transcriptomic, proteomic, epigenetic, and metabolic approaches.

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Immunotherapy has emerged as a promising approach in the field of cancer treatment, with chimeric antigen receptor (CAR) T-cell therapy demonstrating remarkable success. However, challenges such as tumor antigen heterogeneity, immune evasion, and the limited persistence of CAR-T cells have prompted the exploration of alternative cell types for CAR-based strategies. Gamma delta T cells, a unique subset of lymphocytes with inherent tumor recognition capabilities and versatile immune functions, have garnered increasing attention in recent years.

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