Publications by authors named "F Di Paola"

WNT3A is an intestinal ligand triggering the Wnt/β-catenin (Wnt) pathway, which can be enhanced by R-spondin 1 (RSPO1) through the RSPO1-LGR axis or antagonized by the adenomatous polyposis coli (APC) protein supporting β-catenin-degradation. Wnt interplays with several pathways including PI3K/mTOR (mTOR). In this study, we evaluated the influence of WNT3A-commercial and home-made culture media and RSPO1 protein on the Wnt and mTOR interplay in non-APC and APC-mutated intestinal patient-derived organoids (PDOs).

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Article Synopsis
  • The study investigates the role of Wnt/β-catenin and PI3K/mTOR signaling pathways along with gut microbiota in the development of colorectal cancer (CRC), highlighting their significance in familial adenomatous polyposis (FAP) and sporadic cases.
  • Both pathways showed hyperactivation in FAP lesions compared to classic CRC, with specific microbiota compositions linked to these signaling alterations.
  • Overall, the research identifies new biomarkers and therapeutic targets that could enhance prevention and early detection of CRC and adenomas.
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Introduction: Attention to work addiction risk is growing; however, more studies are needed to explore the possible impact of work addiction risk on various aspects of employees' work and life domains. Although several studies have considered the antecedents or consequences of work addiction risk, this study particularly focuses on sleep quality as a potential explanatory underlying mechanism in the relation between work addition risk and three outcome variables including stress at home, stress at work and well-being.

Method: The data was collected using an online platform and participants consisted of 188 French employees who were selected using simple random sampling method.

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: Anticoagulation for venous thromboembolism (VTE) is required for at least three to six months; however, it is advisable to extend the duration in certain cases, in which case a reduced dose of Direct Oral Anticoagulants (DOACs) may be an option. Our objective was to investigate the efficacy and safety of reduced-dose DOACs in extended anticoagulation treatment compared to full doses. : This retrospective single-centre study included 185 patients treated with DOACs for at least 6 months who were divided into two groups: (1) the Full Dose (FD) group (n = 113) and (2) the Reduced Dose (RD) group (n = 72), which included patients treated with Apixaban at 2.

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