Hopp til hovedinnholdet

Publications

NIBIOs employees contribute to several hundred scientific articles and research reports every year. You can browse or search in our collection which contains references and links to these publications as well as other research and dissemination activities. The collection is continously updated with new and historical material.

2024

Abstract

• For more than 20 years, methyl jasmonate (MeJA) has been used to study inducible defenses in conifers and to increase tree resistance to pests and pathogens. Despite the numerous studies on the subject, no attempts have been made to summarize or quantify how MeJA affects resistance and growth in conifers. Here we present a quantitative meta-analysis of the effects of MeJA treatment on the conifer genera Pinus and Picea, two of the most economically and ecologically important tree genera in boreal, temperate, and alpine forests. • A literature search yielded 120 relevant papers. We summarized the key experimental methods used in these papers and performed a meta-analysis of how MeJA affects tree growth and resistance to pests and pathogens. • The results show that MeJA negatively affects tree growth, with an overall effect size of −0.63. The overall effect size of MeJA for tree resistance was −0.76, indicating that MeJA treatment significantly reduces tree damage caused by biotic stressors. • Although our meta-analysis shows that MeJA is effective in enhancing conifer defenses, there are still gaps in our understanding of the durability and ecological consequences of MeJA treatment. We provide suggestions for how future research should be conducted to address these gaps.

To document

Abstract

Colon cancer is increasing worldwide and is commonly regarded as hormone independent, yet recent reports have implicated sex hormones in its development. Nevertheless, the role of hormones from the hypothalamus–hypophysis axis in colitis-associated colorectal cancer (CAC) remains uncertain. In this study, we observed a significant reduction in the expression of the oxytocin receptor (OXTR) in colon samples from both patient with colitis and patient with CAC. To investigate further, we generated mice with an intestinal-epithelium-cell-specific knockout of OXTR. These mice exhibited markedly increased susceptibility to dextran-sulfate-sodium-induced colitis and dextran sulfate sodium/azoxymethane-induced CAC compared to wild-type mice. Our findings indicate that OXTR depletion impaired the inner mucus of the colon epithelium. Mechanistically, oxytocin was found to regulate Mucin 2 maturation through β1-3-N-acetylglucosaminyltransferase 7 (B3GNT7)-mediated fucosylation. Interestingly, we observed a positive correlation between B3GNT7 expression and OXTR expression in human colitis and CAC colon samples. Moreover, the simultaneous activations of OXTR and fucosylation by l-fucose significantly alleviated tumor burden. Hence, our study unveils oxytocin’s promising potential as an affordable and effective therapeutic intervention for individuals affected by colitis and CAC.