Publications by authors named "S Rosello"

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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Melon landraces are highly appreciated by consumers who pay price premiums to compensate for lower yields, enabling on-farm conservation. However, they are highly susceptible to soilborne diseases. This study analyses the impact of Cucurbita and Cucumis rootstocks on the accumulation of flavor-related metabolites in Spanish landraces of the Ibericus melon group, as a strategy to promote their sustainable cultivation.

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Background: In the setting of localized colon cancer (CC), circulating tumor DNA (ctDNA) monitoring in plasma has shown potential for detecting minimal residual disease (MRD) and predicting a higher risk of recurrence. With the tumor-only sequencing approach, however, germline variants may be misidentified as somatic variations, precluding the possibility of tracking in up to 11% of patients due to a lack of known somatic mutations. In this study, we assess the potential value of adding white blood cells (WBCs) to tumor tissue sequencing to enhance the accuracy of sequencing results.

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