World Society of Emergency Surgery (WSES) guidelines for management of skin and soft tissue infections

Peer reviewe

Biomass-dependent Effects of Age-0 Common Carp on Aquatic Ecosystems

Fishes play a functional role in structuring aquatic ecosystems through top-down and bottom-up processes. Adult common carp (Cyprinus carpio) are well recognized for their middle-out effects on aquatic ecosystems that can shift shallow lakes from the clear- to turbid-water stable state through benthic foraging activities. However, less is known about ecosystem effects of age-0 common carp. Age-0 common carp are planktivorous and can be highly abundant, suggesting that large year classes may also produce undesirable ecosystem effects. We evaluated the effects of four age-0 common carp densities (0, 175, 475, and 812 kg/ha) on water quality (ammonium, total phosphorus, total Kjeldahl nitrogen, and turbidity) and primary (macrophytes and phytoplankton) and secondary (zooplankton and benthic invertebrates) production. Common carp increased nutrient availability and phytoplankton production and decreased water transparency with effects increasing with carp biomass. Common carp also reduced macrophyte coverage and cladocera density (through effects on chydorus and ceriodaphnia) and body size, but effects were not density dependent. In contrast, common carp did not appear to affect copepod, rotifer, chironomid, or gastropod densities. These results suggest that even relatively low age-0 common carp densities (\u3e175 kg/ha) may have many comparable ecosystem effects as adult carp, although effects may be accrued through different pathways

Src kinases in chondrosarcoma chemoresistance and migration: dasatinib sensitises to doxorubicin in TP53 mutant cells

BACKGROUND: Chondrosarcomas are malignant cartilage-forming tumours of bone. Because of their resistance to conventional chemotherapy and radiotherapy, currently no treatment strategies exist for unresectable and metastatic chondrosarcoma. Previously, PI3K/AKT/GSK3β and Src kinase pathways were shown to be activated in chondrosarcoma cell lines. Our aim was to investigate the role of these kinases in chemoresistance and migration in chondrosarcoma in relation to TP53 mutation status. METHODS: We used five conventional and three dedifferentiated chondrosarcoma cell lines and investigated the effect of PI3K/AKT/GSK3β pathway inhibition (enzastaurin) and Src pathway inhibition (dasatinib) in chemoresistance using WST assay and live cell imaging with AnnexinV staining. Immunohistochemistry on tissue microarrays (TMAs) containing 157 cartilaginous tumours was performed for Src family members. Migration assays were performed with the RTCA xCelligence System. RESULTS: Src inhibition was found to overcome chemoresistance, to induce apoptosis and to inhibit migration. Cell lines with TP53 mutations responded better to combination therapy than wild-type cell lines (P=0.002). Tissue microarray immunohistochemistry confirmed active Src (pSrc) signalling, with Fyn being most abundantly expressed (76.1%). CONCLUSION: These results strongly indicate Src family kinases, in particular Fyn, as a potential target for the treatment of inoperable and metastatic chondrosarcomas, and to sensitise for doxorubicin especially in the presence of TP53 mutations