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Nolting, J.

Publications and source records attributed to Nolting, J..

3 recordsLinked to original sources

A mixture of plant polyphenols unexpectedly aggravates liver metastasis of colorectal cancer in mice

Epidemiological studies suggest that vegetarian diets are associated with lower cancer incidence and mortality, an effect attributed in part to phytochemicals such as polyphenols and carotenoids. Although numerous in vitro experiments and investigations using immunodeficient rodent models report tumor-suppressive activities of phytochemicals, their impact on tumor progression in immunocompetent hosts remains insufficiently understood. Here, we examined the influence of a defined plant phytochemical mixture (PPM) on the growth of colon cancer liver metastases, both in vitro and in immunocompetent mice. Consistent with the prevailing literature, treatment of the murine colon cancer cell line MC38 with the PPM significantly reduced cell proliferation and survival in vitro. Strikingly, however, administration of the PPM to mice bearing MC38-derived hepatic metastases markedly accelerated tumor growth. Immunohistochemical analyses revealed a significantly increased accumulation of immune cells--specifically CD45 leukocytes and F4/80 macrophages--at the periphery of the metastatic lesions in PPM-treated animals. To assess the functional relevance of this inflammatory response, the PPM was combined with the anti-inflammatory drug prednisolone. This intervention resulted in significantly reduced metastatic burden, supporting the notion that the PPM exacerbates tumor progression through enhanced peritumoral inflammation. These findings highlight the importance of validating observations from cell culture and immunodeficient models in fully immunocompetent systems. They further emphasize that the immunomodulatory effects of plant phytochemicals warrant careful and comprehensive investigation.

cancer biology↗

Shift in cellular crosstalk reveals the immunosuppressive environment in cholangiocarcinoma patients.

Background and aimsCholangiocarcinoma (CCA) is a deadly disease, and this cancer entity is characterized by an abundant stroma. The tumor microenvironment (TME) plays an important role in aggressive behavior and poor response to therapeutics; however, underlying pathways are unknown. MethodsTo fill this gap, we used multiplexed immunohistochemistry, high-dimensional phenotyping, and transcriptomics to analyze human CCA samples and identify cell cluster crosstalk in patients with a poor prognosis. ResultsOur findings confirmed the presence of Tregs and the lack of effector memory cells in the tumor. New findings are the spatiality of the effector memory cells being more present in the peripheral tissue, for some reason these immune cells fail to reach the tumor niche. We revealed cancer crosstalk with macrophages and stromal cells and identified responsible genes in the poor prognosis group. Amongst the responsible ligand pairs are GAS6-AXL belonging to the TAM family. We then identified VCAN-TLR2 to be present and influencing the ECM in a way to supports immune exhaustion. Last, EGFR-TGF-{beta} is expressed in macrophages and this finding is important in Tregs induction and blocking cytotoxic T cell function. ConclusionsThe multiple mechanisms leading to the exclusion of relevant immune cells needed for an anti-cancer response and mechanisms leading to active immune suppression are part of complex cell-cell crosstalk. This study provides a deeper insight into the immune exhausted phenotype in CCA.

cancer biology↗

Tissue tropisms of avian influenza A viruses affect their spillovers from wild birds to pigs

Wild aquatic birds maintain a large genetically diverse pool of influenza A viruses (IAVs), which can be transmitted to lower mammals and ultimately humans. Through phenotypic analyses, only a small set of avian IAVs replicated well in the epithelial cells of swine upper respiratory tracts, and these viruses were shown to infect and cause virus shedding in pigs. Such a phenotypic trait appears to emerge randomly and are distributed among IAVs across multiple avian species, geographic and temporal orders, and is determined not by receptor binding preference but other markers across genomic segments, such as those in the ribonucleoprotein complex. This study demonstrates that phenotypic variants exist among avian IAVs, only a few of which may result in viral shedding in pigs upon infection, providing opportunities for these viruses to become pig adapted, thus posing a higher potential risk for creating novel variants or detrimental reassortants within pig populations. Author SummaryHaving both avian-like receptors and human-like 2,6-linked sialic acid receptors, swine serve as a "mixing vessel" for generating human influenza pandemic strains. All HA subtypes of IAVs can infect swine; however, only sporadic cases of avian IAVs are reported in domestic swine. The molecular mechanisms affecting avian IAVs ability to infect swine are still not fully understood. Through phenotypic analyses, this study suggested that tissue tropisms (i.e., in swine upper respiratory tracts) of avian IAVs affect their spillovers from wild birds to pigs, and this phenotype was determined not by receptor binding preference but by other markers across genomic segments, such as those in the ribonucleoprotein complex. In addition, our results showed that such a phenotypic trait was sporadically and randomly distributed among IAVs across multiple avian species, geographic and temporal orders. This study suggested an efficient way for risk assessment of avian IAVs, such as in evaluating their potentials to be transmitted from avian to pigs.

microbiology↗