Publications by authors named "C I Abildgaard"

Background: Patients with colorectal metastatic disease have a poor prognosis, limited therapeutic options, and frequent development of resistance. Strategies based on tumor-derived organoids are a powerful tool to assess drug sensitivity at an individual level and to suggest new treatment options or re-challenge. Here, we evaluated the method's feasibility and clinical outcome as applied to patients with no satisfactory treatment options.

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  • Serous ovarian carcinoma is the most common type of ovarian cancer and has a significant impact on survival, with cancer-associated fibroblasts (CAFs) playing a key role in its growth and spread.
  • The study used RNA sequencing to analyze malignant fluids from ovarian cancer patients and identified important intercellular interactions between CAFs and cancer cells linked to prognosis and treatment response.
  • Findings highlighted specific signaling pathways and ligand-receptor pairs, such as THBS2/THBS3 and MDK interactions, which are potential therapeutic targets and are associated with poorer overall survival in patients.
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Genetic and epigenetic changes contribute to intratumor heterogeneity and chemotherapy resistance in several tumor types. LncRNAs have been implicated, directly or indirectly, in the epigenetic regulation of gene expression. We investigated lncRNAs that potentially mediate carboplatin-resistance of cell subpopulations, influencing the progression of ovarian cancer (OC).

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Objectives: To identify individual characteristics associated with serological COVID-19 vaccine responsiveness and the durability of vaccine-induced antibodies.

Methods: Adults without history of SARS-CoV-2 infection from the Danish population scheduled for SARS-CoV-2 vaccination were enrolled in this parallel group, phase 4 study. SARS-CoV-2 Spike IgG and Spike-ACE2-receptor-blocking antibodies were measured at days 0, 21, 90, and 180.

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  • Metastatic melanoma often resists current immune and targeted therapies, necessitating new treatment approaches focused on cellular metabolism.
  • Researchers screened 180 metabolic modulators, identifying two candidates—4-methylumbelliferone (4-MU) and ursolic acid (UA)—that showed promise in inhibiting melanoma cell growth, especially when combined with the BRAF inhibitor vemurafenib.
  • Further analysis revealed that 4-MU inhibited glycolysis, enhancing vemurafenib's effectiveness, while UA increased glycolysis and altered mitochondrial respiration, ultimately leading to greater cancer cell death and suggesting oxidative stress plays a role in this process.
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