Publications by authors named "M F Magliano"

Pancreatic ductal adenocarcinoma has a unique tumor microbiome and the systemic depletion of bacteria or fungi using antibiotic/antifungal cocktails leads to a decrease in pancreatic tumor burden in mice. However, functional studies remain rare due to the limited availability of clinically relevant microbiota. Here, we describe in detail the isolation of bacteria and fungi from the small intestine and tumor of pancreatic cancer patients at the Rogel Cancer Center.

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  • This work presents a new framework to assess the economic value of illegal clearings in the Amazon rainforest using Habitat Equivalency Analysis while focusing on restoring ecosystem services.
  • The framework calculates the economic value by considering both past losses and potential future gains, resulting in a valuation of approximately Int.$ 341,611 for 10 hectares cleared, which is significantly higher than traditional timber-focused valuations.
  • The approach emphasizes low costs and efficiency, making it useful for preliminary environmental assessments and enhancing understanding of the financial impacts of deforestation in the Amazon.
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Objective: This study focused on the development of a new-to-world ingredient harnessing the natural potential of fresh Jasminum grandiflorum flowers to self-ferment by its phytobiome revealing flower content. Analytical investigations were conducted to highlight specific phytocompounds generated during the natural fermentation of flowers in comparison to a conventional extraction. The synergy with another extraction technology maximized the generation of biocompounds for an interesting efficacy.

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Aberrant activation of GLI transcription factors has been implicated in the pathogenesis of different tumor types including pancreatic ductal adenocarcinoma. However, the mechanistic link with established drivers of this disease remains in part elusive. In this study, using a new genetically engineered mouse model overexpressing constitutively active mouse form of GLI2 and a combination of genome-wide assays, we provide evidence of a novel mechanism underlying the interplay between KRAS, a major driver of pancreatic ductal adenocarcinoma development, and GLI2 to control oncogenic gene expression.

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  • Tumor progression leads to fibrosis, which involves excessive buildup of extracellular matrix and reduces immune cell infiltration, particularly affecting CD8 T cells.
  • Tumor-associated macrophages (TAMs) adapt to the stiff fibrotic environment by promoting collagen production through signaling from transforming growth factor-β.
  • This collagen production by TAMs creates a challenging metabolic environment that limits the effectiveness of CD8 T cells, hindering their ability to mount strong antitumor responses in breast cancer patients.
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