A recent study investigated using #CLDN1_specific #monoclonal_antibody (mAb) in treating #hepatocellular_carcinoma (HCC). This study targeting non-junctional CLDN1 suppressed tumor growth and invasion in cell line-based models of #HCC and patient-derived 3D ex vivo models. This article suggested that CLDN1 regulates tumor stemness, metabolism, and oncogenic signalling and perturbs the tumor immune microenvironment. Therefore, targeting CLDN1 in HCC and clinical development of CLDN1-specific mAbs can be a breakthrough in the treatment process of advanced HCC. Ref: https://lnkd.in/e_Favmib #HCC #Immunotherapy
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Malignant #melanoma represents the most fatal #skin #cancer due to its aggressive biological behavior and high metastatic potential. In this #review, the authors summarized novel #tumor metabolic pathways and tumor-host metabolic crosstalk mechanisms leading to melanoma progression and drug resistance, with an overview on their translational potential as novel therapeutic targets. 📝 Metabolic Interplay between the Immune System and Melanoma Cells: Therapeutic Implications — Indini et al. Full text is available ➡️ https://lnkd.in/dyh4zNUg #biomarkers #medicalsciences #health #cancertreatment #medicine #metabolism
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#CancerCell: #Tumor microbiota can produce active metabolites that affect cancer and #immune cell signaling, #metabolism, and #proliferation. The study demonstrated that #lactic acid bacteria in the tumor #microenvironment can alter tumor metabolism and lactate signaling pathways, causing therapeutic resistance. In other words, Lactic acid bacteria could be promising therapeutic targets across cancer types. https://lnkd.in/gtDZtywP For more push, please follow #Twitter: https://lnkd.in/gntQ9qE7 Related Product Recommendation: #Gemcitabine (https://lnkd.in/gGbhxJ7S); #Phytohemagglutinin (https://lnkd.in/gJhds-96); #Hyaluronidase (https://lnkd.in/gjxkkv82); #A83-01 (https://lnkd.in/gQtHZhZf); #Forskolin (https://lnkd.in/gE_WVqZC).
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Lactate dehydrogenase A (LDHA) promotes glioblastoma progression by facilitating interaction between tumor cells and macrophages. Inhibiting LDHA disrupts this interaction, suppressing tumor growth and reducing macrophage infiltration. LDHA and its downstream signals are suggested as potential biomarkers and therapeutic targets for glioblastoma treatment. 💯 ✨ 🎉 🎊 #naturejournals #naturecommunications #glioblastoma #cancerresearch #2024goals 🤲 https://lnkd.in/dDywzfCm
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The mechanisms underlying #enhanced #immunotherapy efficacy through #exercise. (A) The #antitumor effects of exercise depend on IL-15 signaling pathway, thus enhancing the sensitivity of pancreatic tumor cells to immunotherapy. (B) Exercise increases the infiltration of CD8+ T cells through the CXCL9 or CXCL11/CXCR3 signaling pathway. (C) Exercise influences multiple transcriptional pathways, including promotion of vascular branching and normal vasoconstriction, which improves hypoxia in TME and enhances the efficiency of drug transport.
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In pancreatic ductal adenocarcinoma (PDAC), glutamine (Gln) is vital for cell proliferation and redox balance. Yet initial efforts to inhibit its metabolism did not succeed--they encountered issues of metabolic reprogramming and therapy resistance. Joel Encarnación-Rosado et al. identified 6-diazo-5-oxo-L-norleucine (DON) and its pro-drug version, sirpiglenastat (DRP-104), as effective Gln antagonists. Their research shows that DON induced a metabolic crisis in vitro, and DRP-104 significantly reduced tumor growth in vivo. These research suggests a potential change in treatment approaches and point to a prospective therapeutic path for PDAC. Explore further by clicking here:https://lnkd.in/eDAKyQU6
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Remove the guesswork from circulating tumor cell ernumeration: https://lnkd.in/gcrNcy7i Our new validated antibodies for use with the Genesis System and Celselect Slides™ Enumeration Direct and Indirect Stain Kits provide sensitive and specific immunostaining of CTC surface biomarkers. #CTCEnumeration #CancerResearch #BioRadGenesis
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New Small Molecule! AM580, a benzoic derivative of retinoic acid and a selective RAR-α agonist, has been shown to significantly reduce the production of Th1 cytokines but promote Th2 cytokines in human PBMCs7 and to inhibit microglial activation, thus acting beneficially in Alzheimer's disease treatment. It also is known to inhibit tumor cell proliferation and induces apoptosis.. #smallmolecules More details: https://bit.ly/3jlS3o6
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🔬 Exciting new research! HPN-AS1, mediated by GABPA, shows potential as a tumor suppressor in hepatocellular carcinoma (HCC). 🌟 It inhibits cell proliferation and promotes apoptosis by facilitating eIF4A3 degradation. Could HPN-AS1 be a future biomarker or therapeutic target for HCC? 🧬 👉 https://lnkd.in/dsyu9YaJ #TurkishJournalofGastroenterology #TJG #GastroenterologyResearch #MedicalJournals #GastrointestinalResearch #July #NewIssue #HepatocellularCarcinoma #CancerResearch #BiomedicalScience
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#CancerCell: The study found that #Aspergillus sydowii, the enriched tumor-resident fungus, promotes lung adenocarcinoma progression by inducing #MDSCs expansion and activation through #IL-1β secretion via β-glucan mediated #Dectin1/CARD9 pathway. These findings identify the intratumor mycobiome, despite their low abundance, promotes tumor progression by inducing an immunosuppressive #TME. https://lnkd.in/grP7db-H For more push, please follow #Twitter: https://lnkd.in/gntQ9qE7
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NOW ONLINE This study identified EN1 and TGFβ-EN1 signaling as important features of #AdenoidCysticCarcinoma highlighting the diagnostic promise of EN1 🔓 OPEN ACCESS ➡ https://lnkd.in/eke6S7Av Accurate diagnosis of adenoid cystic carcinoma (ACC) often requires distinction from basal cell adenoma (BCA). Diagnostic markers capable of differentiating ACC from BCA, however, are lacking. Here, the authors investigated the diagnostic potential of homeobox transcription factor EN1. Immunohistochemistry revealed elevated EN1 expression specifically in ACC, enabling differentiation from BCA. Experiments using a translational patient-derived organoid model indicate that EN1 is regulated through TGFβ signaling, wherein TGFβ-induced EN1 promotes tumor budding, and that ACC develops invasive growth characteristics via tumor budding. The findings identify EN1 and TGFβ-EN1 signaling as important features of ACC and highlight the diagnostic promise of EN1.
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