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Träfflista för sökning "WFRF:(Jonasson Pernilla) "

Sökning: WFRF:(Jonasson Pernilla)

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1.
  • Berger, Karoline, 1991, et al. (författare)
  • Interleukin-6 Induces Stem Cell Propagation through Liaison with the Sortilin-Progranulin Axis in Breast Cancer.
  • 2023
  • Ingår i: Cancers. - 2072-6694. ; 15:24
  • Tidskriftsartikel (refereegranskat)abstract
    • Unraveling the complex network between cancer cells and their tumor microenvironment is of clinical importance, as it might allow for the identification of new targets for cancer treatment. Cytokines and growth factors secreted by various cell types present in the tumor microenvironment have the potential to affect the challenging subpopulation of cancer stem cells showing treatment-resistant properties as well as aggressive features. By using various model systems, we investigated how the breast cancer stem cell-initiating growth factor progranulin influenced the secretion of cancer-associated proteins. In monolayer cultures, progranulin induced secretion of several inflammatory-related cytokines, such as interleukin (IL)-6 and -8, in a sortilin-dependent manner. Further, IL-6 increased the cancer stem fraction similarly to progranulin in the breast cancer cell lines MCF7 and MDA-MB-231 monitored by the surrogate mammosphere-forming assay. In a cohort of 63 patient-derived scaffold cultures cultured with breast cancer cells, we observed significant correlations between IL-6 and progranulin secretion, clearly validating the association between IL-6 and progranulin also in human-based microenvironments. In conclusion, the interplay between progranulin and IL-6 highlights a dual breast cancer stem cell-promoting function via sortilin, further supporting sortilin as a highly relevant therapeutic target for aggressive breast cancer.
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2.
  • Berner, Karin, et al. (författare)
  • Dose optimisation of double-contrast barium enema examinations.
  • 2010
  • Ingår i: Radiation protection dosimetry. - : Oxford University Press (OUP). - 1742-3406 .- 0144-8420. ; 139:1-3, s. 388-392
  • Tidskriftsartikel (refereegranskat)abstract
    • The purpose of the present work was to optimise the filtration and dose setting for double-contrast barium enema examinations using a Philips MultiDiagnost Eleva FD system. A phantom study was performed prior to a patient study. A CDRAD phantom was used in a study where copper and aluminium filtration, different detector doses and tube potentials were examined. The image quality was evaluated using the software CDRAD Analyser and the phantom dose was determined using the Monte Carlo-based software PCXMC. The original setting [100 % detector dose (660 nGy air kerma) and a total filtration of 3.5 mm Al, at 81 kVp] and two other settings identified by the phantom study (100 % detector dose and additional filtration of 1 mm Al and 0.2 mm Cu as well as 80 % detector dose and added filtration of 1 mm Al and 0.2 mm Cu) were included in the patient study. The patient study included 60 patients and up to 8 images from each patient. Six radiologists performed a visual grading characteristics study to evaluate the image quality. A four-step scale was used to judge the fulfillment of three image quality criteria. No overall statistical significant difference in image quality was found between the three settings (P > 0.05). The decrease in the effective dose for the settings in the patient study was 15 % when filtration was added and 34 % when both filtrations was added and detector dose was reduced. The study indicates that additional filtration of 1 mm Al and 0.2 mm Cu and a decrease in detector dose by 20 % from the original setting can be used in colon examinations with Philips MultiDiagnost Eleva FD to reduce the patient dose by 30 % without significantly affecting the image quality. For 20 exposures, this corresponds to a decrease in the effective dose from 1.6 to 1.1 mSv.
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  • Flodén, Lotta, et al. (författare)
  • A discussion of a homogenization procedure for a degenerate linear hyperbolic-parabolic problem
  • 2017
  • Ingår i: ICNPAA 2016 World Congress. - Melville, USA : American Institute of Physics (AIP). - 9780735414648
  • Konferensbidrag (refereegranskat)abstract
    • We study the homogenization of a hyperbolic-parabolic PDE with oscillations in one fast spatial scale. Moreover, the first order time derivative has a degenerate coefficient passing to infinity when ε → 0.We obtain a local problem which is of elliptic type, while the homogenized problem is also in some sense an elliptic problem but with the limit for ε−1∂tuε as an undetermined extra source term in the right-hand side. The results are somewhat surprising and work remains to obtain a fully rigorous treatment. Hence the last section is devoted to a discussion of the reasonability of our conjecture including numerical experiments.
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6.
  • Flodén, Liselott, et al. (författare)
  • Homogenization of a Hyperbolic-Parabolic Problem with Three Spatial Scales
  • 2017
  • Ingår i: Progress in Industrial Mathematics at ECMI 2016. - Cham : Springer. - 9783319630816 ; , s. 617-623
  • Konferensbidrag (refereegranskat)abstract
    • We study the homogenization of a certain linear hyperbolic-parabolic problem exhibiting two rapid spatial scales {ε; ε2}. The homogenization is performed by means of evolution multiscale convergence, a generalization of the concept of two-scale convergence to include any number of scales in both space and time. In particular we apply a compactness result for gradients. The outcome of the homogenization procedure is that we obtain a homogenized problem of hyperbolic-parabolic type together with two elliptic local problems, one for each rapid scale, for the correctors.
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  • Hansson, Jonny, et al. (författare)
  • A practical approach to prioritise among optimisation tasks in X-ray imaging: introducing the 4-bit concept
  • 2010
  • Ingår i: Radiation protection dosimetry. - : Oxford University Press (OUP). - 1742-3406 .- 0144-8420. ; 139:1-3, s. 393-399
  • Tidskriftsartikel (refereegranskat)abstract
    • According to European and national legislation, as well as international recommendations, X-ray examinations shall be optimised. However, with limited resources and hundreds of different types of X-ray examinations, it may be difficult to prioritise among the optimisation tasks at a radiology department. This work is focused on describing a method that can be used to determine the order of which the examinations should be optimised. In the Medical Exposure Directive from 1997, the European Commission prescribes the content of an optimisation process in relation to medical exposure. A reasonable interpretation of the directive is that the assurance of medical purpose for a justified examination is superior to the need of decreased radiation dose. This was used as a basis for developing a method for prioritisation among optimisation tasks. For each examination type, the following four yes/no questions are raised: (i) Is the present image quality unacceptable? (ii) Is the examination of particular importance? (iii) Is the radiation dose suspiciously high? (iv) Are there special dose level concerns, e.g. diagnostic reference levels? Arguing that a positive response to any of the four questions results in the examination being higher prioritised than otherwise and that the questions are labelled in order of decreasing relevance, it can be shown that the resulting flow chart, determining the order of which the examinations should be optimised, can be described by a 4-bit binary scale. In this way, each examination type is given a number from 0 to 15, a higher number corresponding to the examination being prioritised higher in the optimisation work. The method was applied to a general radiology department and resulted in a well-discriminated distribution of examinations prioritised for optimisation tasks. In conclusion, taking into account both medical outcome and potential risk, the proposed method can be used to determine the order in which examinations at a radiology department should be optimised.
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  • Landberg, Göran, 1963, et al. (författare)
  • Characterization of cell-free breast cancer patient-derived scaffolds using liquid chromatography-mass spectrometry/mass spectrometry data and RNA sequencing data
  • 2020
  • Ingår i: Data in Brief. - : Elsevier BV. - 2352-3409. ; 31
  • Tidskriftsartikel (refereegranskat)abstract
    • Patient-derived scaffolds (PDSs) generated from primary breast cancer tumors can be used to model the tumor microenvironment in vitro . Patient-derived scaffolds are generated by repeated detergent washing, removing all cells. Here, we analyzed the protein composition of 15 decellularized PDSs using liquid chromatography-mass spectrometry/mass spectrometry. One hundred forty-three proteins were detected and their relative abundance was calculated using a reference sample generated from all PDSs. We performed heatmap analysis of all the detected proteins to display their expression patterns across different PDSs together with pathway enrichment analysis to reveal which processes that were connected to PDS protein composition. This protein dataset together with clinical information is useful to investigators studying the microenvironment of breast cancers. Further, after repopulating PDSs with either MCF7 or MDA-MB-231 cells, we quantified their gene expression profiles using RNA sequencing. These data were also compared to cells cultured in conventional 2D conditions, as well as to cells cultured as xenografts in immune-deficient mice. We investigated the overlap of genes regulated between these different culture conditions and performed pathway enrichment analysis of genes regulated by both PDS and xenograft cultures compared to 2D in both cell lines to describe common processes associated with both culture conditions. Apart from our described analyses of these systems, these data are useful when comparing different experimental model systems. Downstream data analyses and interpretations can be found in the research article "Patient-derived scaffolds uncover breast cancer promoting properties of the microenvironment" [1] . (C) 2020 The Authors. Published by Elsevier Inc.
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