| 1. |
- Abbafati, Cristiana, et al.
(author)
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- 2020
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Journal article (peer-reviewed)
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| 2. |
- Sgaramella, Nicola, et al.
(author)
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Expression of p16 in squamous cell carcinoma of the mobile tongue is independent of HPV infection despite presence of the HPV-receptor syndecan-1
- 2015
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In: British Journal of Cancer. - : Nature Publishing Group. - 0007-0920 .- 1532-1827. ; 113:2, s. 321-326
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Journal article (peer-reviewed)abstract
- Background: Tongue squamous cell carcinoma (TSCC) is increasing in incidence, especially among young patients and preferably females. Infection with human papilloma virus (HPV) has been suggested as a cause of SCC in the head and neck, and the proportion of oropharyngeal cancers caused by HPV has steadily increased. Methods: Samples from 109 patients with primary TSCC were analysed for the presence of HPV16 by in situ hybridisation and for expression of its surrogate marker p16 and the HPV receptor syndecan-1 by immunhistochemistry. Results: No evidence of HPV16 DNA was observed in the tumours, although one-third showed p16 staining. There was no difference in the expression of the primary HPV receptor, syndecan-1, between TSCC and a group of tonsil SCC. Conclusion: Whereas p16 is expressed in some TSCCs, HPV16 is undetectable, therefore, p16 cannot be used as a surrogate marker for high-risk HPV-infection in this tumour. Despite presence of the HPV-receptor syndecan-1 in TSCC, HPV prefers the tonsillar environment. Lack of p16 associates with worse prognosis primarily in patients aged <= 40 years with tongue SCC. The improved prognosis seen in p16-positive TSCC can be due to induction of a senescent phenotype or an inherent radiosensitivity due to the ability of p16 to inhibit homologous recombination repair.
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| 3. |
- Bergh, Johan, 1983-, et al.
(author)
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Structural and kinetic analysis of protein-aggregate strains in vivo using binary epitope mapping
- 2015
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In: Proceedings of the National Academy of Sciences of the United States of America. - : National Academy of Sciences. - 0027-8424 .- 1091-6490. ; 112:14, s. 4489-4494
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Journal article (peer-reviewed)abstract
- Despite considerable progress in uncovering the molecular details of protein aggregation in vitro, the cause and mechanism of protein-aggregation disease remain poorly understood. One reason is that the amount of pathological aggregates in neural tissue is exceedingly low, precluding examination by conventional approaches. We present here a method for determination of the structure and quantity of aggregates in small tissue samples, circumventing the above problem. The method is based on binary epitope mapping using anti-peptide antibodies. We assessed the usefulness and versatility of the method in mice modeling the neurodegenerative disease amyotrophic lateral sclerosis, which accumulate intracellular aggregates of superoxide dismutase-1. Two strains of aggregates were identified with different structural architectures, molecular properties, and growth kinetics. Both were different from superoxide dismutase-1 aggregates generated in vitro under a variety of conditions. The strains, which seem kinetically under fragmentation control, are associated with different disease progressions, complying with and adding detail to the growing evidence that seeding, infectivity, and strain dependence are unifying principles of neurodegenerative disease.
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| 4. |
- Danielsson, Karin, et al.
(author)
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Effects of the adsorption of NOM model molecules on the aggregation of TiO2 nanoparticles in aqueous suspensions
- 2018
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In: NanoImpact. - : Elsevier BV. - 2452-0748. ; 10, s. 177-187
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Journal article (peer-reviewed)abstract
- © 2018 Interaction of synthetic TiO2(anatase) nanoparticles in aqueous suspension at pH 5 was investigated as a function of time in the presence of various organic molecules in terms of adsorption and aggregation behaviour. ζ-potential and average particle diameter were determined with electrophoretic and dynamic light scattering, respectively, while batch adsorption experiments were used to quantify the amount of organic ligand adsorbed to the TiO2NP. An IR spectroscopic study was carried out at pH 2.8 and 5 to gain information about the interactions of the adsorbed molecules with the TiO2surface on the molecular level. Furthermore, DLVO calculations provided information about the interaction energies between particles and their tendency to aggregate under some experimental conditions. Colloidal stability of TiO2NPs in the presence of organic molecules was studied during a time period of up to 90 days. Results showed that ligands with different functional groups may interact differently with the surface depending on the type and position of available surface sites, the molecular structure of the ligand and suspension pH. Adsorption, hydrodynamic diameter and ζ-potential were affected by the ligand concentration in all tested systems. Increased concentration gave rise to increased adsorption, while ζ-potential decreased and charge inversion was observed for all tested molecules at pH 5. IR spectroscopic study showed the formation of inner sphere and/or outer sphere complexes depending on pH and type of organic ligand. According to DLVO calculations, the critical coagulation concentration (CCC) indicated a trend of increasing colloidal stability with increased concentration of SRFA at pH 5, which was in agreement with the experimental data.
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| 5. |
- Rankin, Linda, 1987-, et al.
(author)
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Relative Deficiency of Anti-Inflammatory N-Acylethanolamines Compared to Prostaglandins in Oral Lichen Planus
- 2020
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In: Biomedicines. - : MDPI. - 2227-9059. ; 8:11
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Journal article (peer-reviewed)abstract
- Oral lichen planus (OLP) is a chronic inflammatory oromucosal disease. The N-acylethanolamines (NAEs), are a family of endogenous biologically active lipid mediators, with palmitoylethanolamide (PEA) being of particular interest here due to its anti-inflammatory and analgesic properties. In this study using oral mucosa biopsies from OLP patients and healthy controls, we investigated whether NAE synthesis was mobilized in response to the inflammation associated with OLP. PTGS2 levels, coding for cyclooxygenase-2 (COX-2), were increased approximately 4-fold in OLP compared to controls and a significant increase in the ratio of PTGS2 to NAPEPLD, the latter coding for a key enzyme in NAE synthesis, was seen. This was matched by an increased ratio of COX-2-derived prostaglandins to PEA in a second patient cohort. We conclude that there is an imbalance between prostaglandins and PEA in OLP, opening up the possibility that PEA might be a useful treatment for this disorder.
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