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This paper addresses a "wide horizontal rim vessel" belonging to the collection of Fundação Sousa d'Oliveira (Azores). Although its provenance and the circumstances of its discovery are currently unknown, the authors contend that this vessel should be attributed to the Iberian Northwest and, more specifically, to the Portuguese territory, in line with the highly homogenous distribution of this type of pottery. A morphological and stylistic study has been carried out establishing its singularity with regards to the decorative composition of the rim, which is without parallel amongst dozens of vessels of the same "family". During the study of this piece, it has been possible to observe traces of soot and organic residues deposited both on its interior and exterior surfaces, which is recurrent in these vessels. The nature of these substances has never been determined in previous studies. In this article, we present and discuss the results obtained from the chromatographic analyses of the organic residue traces found on the vessel. [ABSTRACT FROM AUTHOR]

The role of extracellular vesicles (EVs) as mediators of cell-to-cell communication in cancer progression is widely recognized. In vitro studies are routinely performed on 2D culture models, but recent studies suggest that 3D cultures could represent a more valid model. Human ovarian cancer cells CABA I were cultured by the hanging drop method to form tumor spheroids, that were moved to low adhesion supports to observe their morphology by Scanning Electron Microscopy (SEM) and to isolate the EVs. EVs release was verified by SEM and their identity confirmed by morphology (Transmission Electron Microscopy, TEM), size distribution (Nanoparticles Tracking Analysis), and markers (CD63, CD9, TSG-101, Calnexin). CABA I form spheroids with a clinically relevant size, above 400 μm; they release EVs on their external surface and also trap "inner" EVs. They also produce vasculogenic mimicry-like tubules, that bulge from the spheroid and are composed of a hollow lumen delimited by tumor cells. CABA I can be grown as multicellular spheroids to easily isolate EVs. The presence of features typical of in vivo tumors (inner entrapped EVs and vasculogenic mimicry) suggests their use as faithful experimental models to screen therapeutic drugs targeting these pro-tumorigenic processes. [ABSTRACT FROM AUTHOR]