Publications by authors named "Camblor D"

Background: Circulating tumor DNA (ctDNA) analysis has emerged as a minimally invasive tool for detecting minimal residual disease (MRD) in colorectal cancer (CRC) patients. This enables dynamic risk stratification, earlier recurrence detection, and optimized post-surgical treatment. Two primary methodologies have been developed for ctDNA-based MRD detection: tumor-informed strategies, which identify tumor-specific mutations through initial tissue sequencing to guide ctDNA monitoring, and tumor-agnostic approaches, which utilize predefined panels to detect common cancer-associated genomic or epigenomic alterations directly from plasma without prior tissue analysis.

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Article Synopsis
  • Understanding how pancreatic ductal adenocarcinoma (PDAC) progresses and developing targeted therapies is crucial, and this study involved 80 metastatic PDAC patients divided into discovery and validation groups to examine genetic variants.
  • Whole exome sequencing (WES) of tumor and plasma samples highlighted that actionable mutations were more prevalent in plasma, and associations with cellular organization pathways were found in patients with shorter survival.
  • Notably, KRAS mutations in plasma were linked to worse progression free survival, while significant reductions in KRAS variant allele frequency correlated with improved outcomes similar to KRAS-negative patients, emphasizing the relevance of immune response pathways in liver metastasis.
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The NF-κB signaling pathway is a key regulator of inflammation in the response to SARS-CoV-2 infection. This pathway has been implicated in the hyperinflammatory state that characterizes the severe forms of COVID-19. The genetic variation of the NF-κB components might thus explain the predisposition to critical outcomes of this viral disease.

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