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BACKGROUND: As for many other Azorean Islands, the macroalgal flora of Terceira (belonging to the central group of the archipelago) is poorly known, the published information reflecting occasional collections of sporadic visitors to the island. In order to overcome this and contribute to improve the knowledge of Azorean macroalgal flora at both local and regional scales, a thorough investigation was conducted. Both collections and presence data recordings were undertaken at the littoral and sublittoral levels down to approximately 40 m around the island, covering a total area of approximately 49 km2. This paper lists the taxonomic records and provides information on each species' ecology and occurrence on the Island's littoral. NEW INFORMATION: A total of 418 specimens (including taxa identified only to genus level) belonging to 147 taxa of macroalgae, comprising 95 Rhodophyta, 33 Chlorophyta and 19 Ochrophyta (Phaeophyceae) are registered. Of these, 113 were identified to species level (73 Rhodophyta, 24 Chlorophyta and 16 Ochrophyta), encompassing 35 new records for the Island (27 Rhodophyta, 6 Chlorophyta and 2 Ochrophyta). Most species are native, including the Macaronesian endemisms Codium elisabethiae O.C.Schmidt, Millerella tinerfensis (Seoane-Camba) S.M.Boo & J.M.Rico and Phyllophora gelidioides P.Crouan & H.Crouan ex Karsakoff. Eight species are introduced and 15 have uncertain origin. ; This research was supported by the project "CAMAG/TER - Caracterização das massas de água costeira da Ilha Terceira", funded by the Azores Regional Government and lately by the project "ACORES-01-0145-FEDER-000072" funded the Operational Programme Azores 2020 (85% ERDF and 15% regional funds). Afonso Prestes was supported by a PhD grant (M3.1.a/F/083/2015) awarded by Fundo Regional da Ciência e Tecnologia (FRCT). ; info:eu-repo/semantics/publishedVersion

BACKGROUND: The seaweed flora of Pico Island (central group of the Azores archipelago) has attracted interest of researchers on past occasions. Despite this, the macroalgal flora of the island cannot be considered well-known as published information reflects only occasional collections. To overcome this, a thorough investigation encompassing collections and presence data recording was undertaken. Research under the Campaigns "AÇORES/89", "PICO/91", "PICOBEL/2007" and "LAUMACAT/2011" covered a relatively large area (approximately 39 km2) around the island, encompassing the littoral and sublittoral levels down to about 40 m around the Island.This paper improves the knowledge of the Azorean macroalgal flora at local and regional scales by listing taxonomic records and providing information on the ecology and occurrence of each species present on the Island's littoral. NEW INFORMATION: A total of 4043 specimens (including taxa identified only to genus level) belonging to 303 taxa of macroalgae are registered, comprising 197 Rhodophyta, 53 Chlorophyta and 53 Ochrophyta (Phaeophyceae). From these, 225 were identified to species level (142 Rhodophyta, 41 Chlorophyta and 42 Ochrophyta), encompassing 110 new records for the island (69 Rhodophyta, 20 Chlorophyta and 21 Ochrophyta), three Macaronesian endemisms (Botryocladia macaronesica Afonso-Carillo, Sobrino, Tittley & Neto; Laurencia viridis Gil-Rodríguez & Haroun; Codium elisabethiae O. C. Schmidt), 14 introduced and 25 species with an uncertain status. ; This research was supported by the project "PICOBEL: Coastal benthic communities of Pico Island: characterization and monitoring", funded by the Azores Regional Government and lately by the project "ACORES-01-0145-FEDER-000072" funded the Operational Programme Azores 2020 (85% ERDF and 15% regional funds). Afonso Prestes was supported by a PhD grant (M3.1.a/F/083/2015) awarded by Fundo Regional da Ciência e Tecnologia (FRCT). ; info:eu-repo/semantics/publishedVersion

Background Terminal a2-3 and a2-6 sialylation of glycans precludes further chain elongation, leading to the biosynthesis of cancer relevant epitopes such as sialyl-Lewis X (SLe X ). SLe X overexpression is associated with tumor aggressive phenotype and patients' poor prognosis. Methods MKN45 gastric carcinoma cells transfected with the sialyltransferase ST3GAL4 were established as a model overexpressing sialylated terminal glycans. We have evaluated at the structural level the glycome and the sialoproteome of this gastric cancer cell line applying liquid chromatography and mass spectrometry. We further validated an identified target expression by proximity ligation assay in gastric tumors. Results Our results showed that ST3GAL4 overexpression leads to several glycosylation alterations, including reduced O-glycan extension and decreased bisected and increased branched N-glycans. A shift from a2-6 towards a2-3 linked sialylated N-glycans was also observed. Sialoproteomic analysis further identified 47 proteins with significantly increased sialylated N-glycans. These included integrins, insulin receptor, carcinoembryonic antigens and RON receptor tyrosine kinase, which are proteins known to be key players in malignancy. Further analysis of RON confirmed its modification with SLe X and the concomitant activation. SLe X and RON co-expression was validated in gastric tumors. Conclusion The overexpression of ST3GAL4 interferes with the overall glycophenotype of cancer cells affecting a multitude of key proteins involved in malignancy. Aberrant glycosylation of the RON receptor was shown as an alternative mechanism of oncogenic activation. General significance This study provides novel targets and points to an integrative tumor glycomic/proteomic-profiling for gastric cancer patients' stratification. This article is part of a Special Issue entitled "Glycans in personalised medicine" Guest Editor: Professor Gordan Lauc. ; We acknowledge the support from the European Union, Seventh Framework Programme, Gastric Glyco Explorer initial training network: grant number 316929. IPATIMUP integrates the i3S Research Unit, which is partially supported by FCT, the Portuguese Foundation for Science and Technology. This work is funded by FEDER funds through the Operational Programme for Competitiveness Factors-COMPETE (FCOMP-01-0124-FEDER028188) and National Funds through the FCT-Foundation for Science and Technology, under the projects: PEst-C/SAU/LA0003/2013, PTDC/BBB-EBI/0786/2012, and PTDC/BBB-EBI/0567/2014 (to CAR). This work was also supported by"Glycoproteomics" project grant number PCIG09-GA-2011-293847(to DK) and the Danish Natural Science Research Council and a generous grant from the VILLUM Foundation to the VILLUM Center for Bioanalytical Sciences at the University of Southern Denmark (to MRL). Grants were received from FCT, POPH (Programa Operacional Potencial Humano) and FSE (Fundo Social Europeu): SFRH/BPD/75871/2011 to AM; SFRH/BPD/111048/2015 to JAF; SFRH/BPD/96510/2013 to CG. The UPLC instrument was obtained with a grant from the Ingabritt and Arne Lundbergs Research Foundation (to NK). C.J. was supported by the Knut and Alice Wallenberg Foundation. The mass spectrometer (LTQ) was obtained by a grant from the Swedish Research Council (342-2004-4434) (to NK).