Publications by authors named "Gasche C"

Unlabelled: In the gut, microRNAs (miRNAs) produced by intestinal epithelial cells are secreted into the lumen and can shape the composition and function of the gut microbiome. Crosstalk between gut microbes and the host plays a key role in irritable bowel syndrome (IBS) and inflammatory bowel diseases, yet little is known about how the miRNA-gut microbiome axis contributes to the pathogenesis of these conditions. Here, we investigate the ability of miR-21, a miRNA that we found decreased in fecal samples from IBS patients, to associate with and regulate gut microbiome function.

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SUMMARYThe human intestinal tract harbors a profound variety of microorganisms that live in symbiosis with the host and each other. It is a complex and highly dynamic environment whose homeostasis directly relates to human health. Dysbiosis of the gut microbiota and polymicrobial biofilms have been associated with gastrointestinal diseases, including irritable bowel syndrome, inflammatory bowel diseases, and colorectal cancers.

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Gastrointestinal biofilms are matrix-enclosed, highly heterogenic and spatially organized polymicrobial communities that can cover large areas in the gastrointestinal tract. Gut microbiota dysbiosis, mucus disruption, and epithelial invasion are associated with pathogenic biofilms that have been linked to gastrointestinal disorders such as irritable bowel syndrome, inflammatory bowel diseases, gastric cancer, and colorectal cancer. Intestinal biofilms are highly prevalent in ulcerative colitis and irritable bowel syndrome patients, and most endoscopists will have observed such biofilms during colonoscopy, maybe without appreciating their biological and clinical importance.

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  • * A study analyzed the presence of archaea in stool samples from patients with IBS and ulcerative colitis (UC), finding that the absence of archaea linked to disrupted gut health and reduced microbial diversity.
  • * The presence of archaea may support better GI homeostasis and fatty acid metabolism, suggesting further research is needed to explore their role in mucosal biofilms and small intestinal bacterial overgrowth.
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Lynch syndrome (LS) is the most prevalent heritable form of colorectal cancer. Its early onset and high lifetime risk for colorectal cancer emphasize the necessity for effective chemoprevention. NFE2L2 (NRF2) is often considered a potential druggable target, and many chemopreventive compounds induce NRF2.

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With increasing urbanization and industrialization, the prevalence of inflammatory bowel diseases (IBDs) has steadily been rising over the past two decades. IBD involves flares of gastrointestinal (GI) inflammation accompanied by microbiota perturbations. However, microbial mechanisms that trigger such flares remain elusive.

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The E3 ubiquitin-ligases are important for cellular protein homeostasis and their deregulation is implicated in cancer. The E3 ubiquitin-ligase Hakai is involved in tumour progression and metastasis, through the regulation of the tumour suppressor E-cadherin. Hakai is overexpressed in colon cancer, however, the implication in colitis-associated cancer is unknown.

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Oral iron promotes intestinal tumourigenesis in animal models. In humans, expression of iron transport proteins are altered in colorectal cancer. This study examined whether the route of iron therapy alters iron transport and tumour growth.

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Background & Aims: Irritable bowel syndrome (IBS) and inflammatory bowel diseases result in a substantial reduction in quality of life and a considerable socioeconomic impact. In IBS, diagnosis and treatment options are limited, but evidence for involvement of the gut microbiome in disease pathophysiology is emerging. Here we analyzed the prevalence of endoscopically visible mucosal biofilms in gastrointestinal disease and associated changes in microbiome composition and metabolism.

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Inflammatory bowel disease is a group of conditions with rising incidence caused by genetic and environmental factors including diet. The chelator ethylenediaminetetraacetate (EDTA) is widely used by the food and pharmaceutical industry among numerous other applications, leading to a considerable environmental exposure. Numerous safety studies in healthy animals have revealed no relevant toxicity by EDTA.

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Background:  Iron deficiency and anemia are common findings in IBD. Treatment of anemia improves quality of life. Neurological symptoms like depression or anxiety are also common in IBD; however, their relationship with ID has not been studied in detail.

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Background & Aims: p21-activated kinase-1 (PAK1) belongs to a family of serine-threonine kinases and contributes to cellular pathways such as nuclear factor-κB (NF-κB), mitogen-activated protein kinase (MAPK), phosphatidylinositol 3-kinase/protein kinase B (PI3K/AKT), and Wingless-related integration site(Wnt)/β-catenin, all of which are involved in intestinal homeostasis. Overexpression of PAK1 is linked to inflammatory bowel disease as well as colitis-associated cancer (CAC), and similarly was observed in interleukin (IL)10 knockout (KO) mice, a model of colitis and CAC. Here, we tested the effects of PAK1 deletion on intestinal inflammation and carcinogenesis in IL10 KO mice.

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  • Colorectal cancer develops due to a combination of genetic mutations, environmental factors, gut inflammation, and the gut microbiome, with Lynch syndrome being a key genetic factor affecting tumor types and locations, particularly in the right side of the colon.
  • A study used MSH2 mice crossed with IL-10 knockout mice to investigate the role of inflammation and gut bacteria in colorectal cancer progression, revealing that inflammation significantly increased tumor formation, especially proximal tumors commonly seen in Lynch syndrome cases.
  • The research found that inflammation altered the composition of gut microbiota, leading to an increase in certain bacterial genera linked to tumor presence and a decrease in others, indicating that chronic inflammation exacerbates cancer development in the context of DNA mismatch repair deficiencies.
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  • Iron deficiency (ID) is widespread and linked not only to anemia but also to an increased risk of thrombosis, which could lead to further complications.
  • In a study using animal models, ID was shown to cause higher platelet counts and larger thrombus sizes, demonstrating a clear connection between ID and increased thrombotic tendency.
  • Iron replacement therapy effectively corrected the changes caused by ID, suggesting it could be a useful preventive measure for thrombotic diseases in patients with chronic illnesses predisposed to thrombosis.
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Recent evidence points to a plausible role of diet and the microbiome in the pathogenesis of both Crohn's disease (CD) and Ulcerative Colitis (UC). Dietary therapies based on exclusion of table foods and replacement with nutritional formulas and/or a combination of nutritional formulas and specific table foods may induce remission in CD. In UC, specific dietary components have also been associated with flare of disease.

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  • Inflammatory bowel disease raises the risk of developing colitis-associated cancer, prompting researchers to examine the impact of diet on this condition.
  • A study using female BALB/c mice demonstrated that a Western-style diet worsened colitis symptoms, altered gut microbiota, and increased tumor growth compared to a standard diet, with clear molecular changes observed.
  • Switching from a Western-style diet to a healthier standard AIN93G diet even after the onset of cancer helped improve colitis symptoms and reduced tumorigenesis, highlighting the potential benefits of dietary changes in managing disease.
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Anti-diabetic drugs modulate p-21 activated kinase (PAK) signaling. : Type 2 diabetes mellitus (T2DM) is a chronic inflammatory disease associated with increased cancer risk. PAK signaling is implicated in cellular homeostasis when regulated, and cancer when unrestrained.

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Inflammatory bowel disease (IBD) is a group of chronic relapsing inflammatory disorders affecting the large and small intestine, with a rising worldwide incidence and prevalence. Anaemia is the most common extraintestinal manifestation of IBD, correlating with disease activity, and tending to relapse even after successful therapy. Iron deficiency is the most common cause; however, it often manifests in combination with anaemia of inflammation.

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  • The study investigates how 5-ASA and AZTP, two treatments for inflammatory bowel disease (IBD), help restore the mucosal barrier that is often disrupted in IBD.
  • Both drugs improve epithelial barrier function by affecting cellular structures and proteins, particularly tight junctions, which are crucial for maintaining the intestinal lining.
  • While 5-ASA supports wound healing and alters cell cycle distribution in epithelial cells, AZTP has antiproliferative effects; both contribute to resolving barrier dysfunction but through different biological mechanisms.
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Iron deficiency (ID) workup is a common challenge for gastrointestinal endoscopy. In premenopausal women current guidelines recommend serologic evaluation of coeliac disease only. Here we systematically tested serologic screening for autoimmune gastritis (AIG) in a large cohort of patients with ID.

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Introduction: Intestinal interposition is a term that describes rare anatomic variations where parts of the colon deviate from their normal intraabdominal position, attaching between two organs. Most patients with colonic interpositions are asymptomatic and diagnosed incidentally by computed tomography or ultrasound. Here we present a case of a symptomatic restrogastric colon, interposing kinked between stomach and pancreas.

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Patients with inflammatory bowel disease (IBD) have a higher risk of developing colitis-associated-cancer (CAC); however, the underlying processes of disease progression are not completely understood. Here, the molecular processes of inflammation-driven colon carcinogenesis were investigated using IL10-deficient mice (IL10 KO). IL10 KO mice were euthanized after development of colitis and dysplasia.

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Microsatellite instability (MSI) is present in ulcerative colitis (UC) and colitis-associated colorectal cancers (CAC). Certain factors released by polymorphonuclear cells (PMNs) may drive mucosal frameshift mutations resulting in MSI and cancer. Here, we applied a co-culture system with PMNs and colon epithelial cells to identify such culprit factors.

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  • HuR is an RNA-binding protein linked to immune regulation and certain cancers, particularly colorectal cancer, by stabilizing mRNAs that promote tumor growth and inflammation.
  • The study found increased levels of HuR in colonic epithelial cells from patients with IBD, FAP, and colorectal cancer, while a small-molecule inhibitor of HuR, MS-444, worsened conditions in a model of IBD but reduced tumors in a FAP model.
  • These findings suggest that HuR plays a crucial role at different stages of colorectal cancer development, indicating potential for HuR inhibition as a preventive strategy for FAP, but caution is needed in patients with IBD.
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