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  1. AU="Bastian, Fabienne"
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  1. Article ; Online: Using fecal immmunochemical cartridges for gut microbiome analysis within a colorectal cancer screening program.

    Brezina, Stefanie / Borkovec, Martin / Baierl, Andreas / Bastian, Fabienne / Futschik, Andreas / Gasche, Nikolaus / Gruenberger, Thomas / Hallas, Michael / Jannsen, Christian / Leeb, Gernot / Lutz, Rebecca / Sladek, Barbara / Gsur, Andrea

    Gut microbes

    2023  Volume 15, Issue 1, Page(s) 2176119

    Abstract: The colorectal cancer (CRC) screening program B-PREDICT is an invited two-stage screening project using a fecal immunochemical test (FIT) for initial screening followed by a colonoscopy for those with a positive FIT. Since the gut microbiome likely plays ...

    Abstract The colorectal cancer (CRC) screening program B-PREDICT is an invited two-stage screening project using a fecal immunochemical test (FIT) for initial screening followed by a colonoscopy for those with a positive FIT. Since the gut microbiome likely plays a role in the etiology of CRC, microbiome-based biomarkers in combination with FIT could be a promising tool for optimizing CRC screening. Therefore, we evaluated the usability of FIT cartridges for microbiome analysis and compared it to Stool Collection and Preservation Tubes. Corresponding FIT cartridges as well as Stool Collection and Preservation Tubes were collected from participants of the B-PREDICT screening program to perform 16S rRNA gene sequencing. We calculated intraclass correlation coefficients (ICCs) based on center log ratio transformed abundances and used ALDEx2 to test for significantly differential abundant taxa between the two sample types. Additionally, FIT and Stool Collection and Preservation Tube triplicate samples were obtained from volunteers to estimate variance components of microbial abundances. FIT and Preservation Tube samples produce highly similar microbiome profiles which cluster according to subject. Significant differences between the two sample types can be found for abundances of some bacterial taxa (e.g. 33 genera) but are minor compared to the differences between the subjects. Analysis of triplicate samples revealed slightly worse repeatability of results for FIT than for Preservation Tube samples. Our findings indicate that FIT cartridges are appropriate for gut microbiome analysis nested within CRC screening programs.
    MeSH term(s) Humans ; Gastrointestinal Microbiome/genetics ; RNA, Ribosomal, 16S/genetics ; Early Detection of Cancer/methods ; Microbiota ; Colorectal Neoplasms/diagnosis ; Feces/microbiology
    Chemical Substances RNA, Ribosomal, 16S
    Language English
    Publishing date 2023-02-16
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2575755-6
    ISSN 1949-0984 ; 1949-0984
    ISSN (online) 1949-0984
    ISSN 1949-0984
    DOI 10.1080/19490976.2023.2176119
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Nanocoating with titanium reduces iC3b- and granulocyte-activating immune response against glutaraldehyde-fixed bovine pericardium: a new technique to improve biologic heart valve prosthesis durability?

    Guldner, Norbert W / Bastian, Fabienne / Weigel, Günther / Zimmermann, Hanngörg / Maleika, Markus / Scharfschwerdt, Michael / Rohde, Daniel / Sievers, Hans-Hinrich

    The Journal of thoracic and cardiovascular surgery

    2012  Volume 143, Issue 5, Page(s) 1152–1159

    Abstract: Objectives: An IgG and granulocyte-activating immune response with secondary dystrophic calcification might be the reason glutaraldehyde (GA)-fixed xenograft valves fail, especially in young patients, who are more immunocompetent than the elderly. ... ...

    Abstract Objectives: An IgG and granulocyte-activating immune response with secondary dystrophic calcification might be the reason glutaraldehyde (GA)-fixed xenograft valves fail, especially in young patients, who are more immunocompetent than the elderly. Titanium nanocoating on GA-fixed bovine pericardium was tested for its ability to prevent major immunoreactions.
    Methods: The immune activity of platelets from GA-fixed bovine pericardium with different treatment procedures was evaluated using the blood from 5 human donors: group I (n = 5), GA fixed as the control; group 2 (n = 5), detoxified with 10% citric acid; group 3 (n = 5), 10% citric acid, aldehyde-dehydrogenase, and a physical plasma treatment; and group 4 (n = 5), treated the same as group 3, but with an additional titanium coat 30 nm in thickness. Titanium deposition was visualized using scanning electron microscopy. IgG deposits (iC3b) were shown by immunostaining and documented as colored pixels (red). The pixels were evaluated electronically. Attracted granulocytes (polymorphonuclear leukocytes) were counted in front of the titanium-coated surface.
    Results: IC3b deposits and polymorphonuclear leukocytes within control group 1 were defined as 100%; in group 2, iC3b was 149% ± 34% and polymorphonuclear leukocytes were 89%, in group 3, IC3b was 102% ± 24% and polymorphonuclear leukocytes were 47%; and in group 4, IC3b had decreased to 38.49% ± 21% (P < .05) and polymorphonuclear leukocyte activation had decreased to 6.3% (P ≤ .01).
    Conclusions: Titanium coating significantly reduced the iC3b and granulocyte activating immune response of GA-fixed pericardium. Therefore, it might prevent relevant immunorejection and increase the durability of GA-fixed bioprosthetic heart valves.
    MeSH term(s) Animals ; Bioprosthesis ; Cattle ; Coated Materials, Biocompatible ; Complement C3b/immunology ; Fixatives/toxicity ; Glutaral/toxicity ; Graft Rejection/immunology ; Graft Rejection/prevention & control ; Graft Survival/drug effects ; Granulocytes/drug effects ; Granulocytes/immunology ; Granulocytes/ultrastructure ; Heart Valve Prosthesis ; Heart Valve Prosthesis Implantation/adverse effects ; Heart Valve Prosthesis Implantation/instrumentation ; Humans ; Immunohistochemistry ; Immunosuppressive Agents/pharmacology ; Materials Testing ; Microscopy, Electron, Scanning ; Nanotechnology ; Organometallic Compounds/pharmacology ; Pericardium/immunology ; Pericardium/transplantation ; Prosthesis Failure ; Tissue Fixation
    Chemical Substances Coated Materials, Biocompatible ; Fixatives ; Immunosuppressive Agents ; Organometallic Compounds ; tetrakis(dimethylamido)titanium ; Complement C3b (80295-43-8) ; Glutaral (T3C89M417N)
    Language English
    Publishing date 2012-05
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3104-5
    ISSN 1097-685X ; 0022-5223
    ISSN (online) 1097-685X
    ISSN 0022-5223
    DOI 10.1016/j.jtcvs.2011.10.076
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: IgG deposition and activation of the classical complement pathway involvement in the activation of human granulocytes by decellularized porcine heart valve tissue.

    Bastian, Fabienne / Stelzmüller, Marie-Elisabeth / Kratochwill, Klaus / Kasimir, Marie-Theres / Simon, Paul / Weigel, Guenter

    Biomaterials

    2008  Volume 29, Issue 12, Page(s) 1824–1832

    Abstract: Decellularization treatment of heart valves has been thought to eliminate tissue immunogenicity. Early failure of tissue-engineered xenogeneic heart valves was seen in children and has been a major drawback in this promising field of research. This study ...

    Abstract Decellularization treatment of heart valves has been thought to eliminate tissue immunogenicity. Early failure of tissue-engineered xenogeneic heart valves was seen in children and has been a major drawback in this promising field of research. This study was designed to characterize the effects of acellular porcine heart valve tissue on immune activation in vitro. Incubation of decellularized porcine tissue with human plasma led to adsorption of IgG, activation of the classical complement pathway and adhesion of activated polymorphonuclear leukocytes (PMN). This inflammatory response was strongly inhibited by proteins extracted from native porcine tissue which might indicate that inhibitors of PMN activation present in the extracellular matrix (ECM) are lost during the decellularization process.
    MeSH term(s) Aged ; Animals ; Cell-Free System/immunology ; Cells, Cultured ; Complement Activation/immunology ; Complement Pathway, Classical/immunology ; Female ; Granulocytes/immunology ; Heart Valves/cytology ; Heart Valves/immunology ; Humans ; Immunoglobulin G/immunology ; Male ; Swine
    Chemical Substances Immunoglobulin G
    Language English
    Publishing date 2008-04
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 603079-8
    ISSN 0142-9612
    ISSN 0142-9612
    DOI 10.1016/j.biomaterials.2008.01.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Decellularized, xenogeneic small-diameter arteries: transition from a muscular to an elastic phenotype in vivo.

    Bergmeister, Helga / Plasenzotti, Roberto / Walter, Ingrid / Plass, Christian / Bastian, Fabienne / Rieder, Erwin / Sipos, Wolfgang / Kaider, Alexandra / Losert, Udo / Weigel, Guenter

    Journal of biomedical materials research. Part B, Applied biomaterials

    2008  Volume 87, Issue 1, Page(s) 95–104

    Abstract: Reports regarding the biocompatibility of xenogeneic, decellularized bioprosthetic implants differ between bioinertness and complete graft degradation. We investigated heparin-crosslinked and nonheparinized, xenogeneic vascular substitutes in a rat model. ...

    Abstract Reports regarding the biocompatibility of xenogeneic, decellularized bioprosthetic implants differ between bioinertness and complete graft degradation. We investigated heparin-crosslinked and nonheparinized, xenogeneic vascular substitutes in a rat model. Porcine arteries (15 x 1.5 mm) were decellularized by multistep detergent and enzymatic techniques, which were followed by heparin-crosslinking in 50% of the implants. Prostheses were implanted into the abdominal aorta of 76 rats for 1 day and up to 6 months. Retrieved specimens were evaluated by histology, immunohistochemistry, laser scanning, and scanning electron microscopy. Graft patency did not differ between groups (97.3%). Heparinized grafts showed a statistically significant lower rate of aneurysm formation (p = 0.04 %). Implants revealed infiltration with granulocytes and macrophages up to 3 months. Recellularization with endothelial cells and myofibroblasts was detectable within 1 month. After 6 months elastin biosynthesis and complete graft remodeling toward an elastic vessel was evident. These results indicate that temporary inflammation does not interfere with long-term vascular remodeling.
    MeSH term(s) Aneurysm/etiology ; Animals ; Aorta, Abdominal/surgery ; Arteries/surgery ; Arteries/transplantation ; Blood Vessel Prosthesis/adverse effects ; Cross-Linking Reagents ; Elasticity ; Endothelial Cells/cytology ; Fibroblasts/cytology ; Granulocytes/pathology ; Heparin ; Inflammation/pathology ; Macrophages/pathology ; Materials Testing ; Phenotype ; Rats ; Swine ; Transplantation, Heterologous/adverse effects ; Transplantation, Heterologous/methods ; Vascular Patency
    Chemical Substances Cross-Linking Reagents ; Heparin (9005-49-6)
    Language English
    Publishing date 2008-04-24
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2099992-6
    ISSN 1552-4981 ; 1552-4973 ; 0021-9304
    ISSN (online) 1552-4981
    ISSN 1552-4973 ; 0021-9304
    DOI 10.1002/jbm.b.31074
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Epithelial splicing regulatory protein 1 and 2 paralogues correlate with splice signatures and favorable outcome in human colorectal cancer.

    Deloria, Abigail J / Höflmayer, Doris / Kienzl, Philip / Łopatecka, Justyna / Sampl, Sandra / Klimpfinger, Martin / Braunschmid, Tamara / Bastian, Fabienne / Lu, Lingeng / Marian, Brigitte / Stättner, Stefan / Holzmann, Klaus

    Oncotarget

    2016  Volume 7, Issue 45, Page(s) 73800–73816

    Abstract: ESRPs are master splice regulators implicated in alternative mRNA splicing programs important for epithelial-mesenchymal transition (EMT) and tumor progression. ESRP1 was identified in some tumors as good or worse predictor of outcome, but in colorectal ... ...

    Abstract ESRPs are master splice regulators implicated in alternative mRNA splicing programs important for epithelial-mesenchymal transition (EMT) and tumor progression. ESRP1 was identified in some tumors as good or worse predictor of outcome, but in colorectal cancer (CRC) the prognostic value of ESRPs and relation with mesenchymal splice variants is not clear. Here, we studied 68 CRC cases, compared tissue expression of ESRPs with clinical data and with EMT gene splice patterns of conditional CRC cells with deficient ESRP1 expression.Around 72% of patients showed global decreased transcript expression of both ESRPs in tumor as compared to matched non-neoplastic colorectal epithelium. Reduction of ESRP1 in tumor cells was evaluated by immunohistochemistry, associated with microsatellite stability and switch to mesenchymal splice signatures of FGFRs, CD44, ENAH and CTNND1(p120-catenin). Expression of ESRPs was significantly associated with favorable overall survival (log-rank test, P=0.0186 and 0.0408), better than prognostic stratification by tumor staging; and for ESRP1 confirmed with second TCGA cohort (log-rank test, P=0.0435). Prognostic value is independent of the pathological stage and microsatellite instability (ESRP1: HR=0.36, 95%CI 0.15-0.91, P=0.032; ESRP2: HR=0.23, 95%CI 0.08-0.65, P=0.006).Our study supports the role of ESRP1 as tumor suppressor and strongly suggests that ESRPs are candidate markers for early detection, diagnosis, and prognosis of CRC.
    Language English
    Publishing date 2016-11-08
    Publishing country United States
    Document type Journal Article
    ISSN 1949-2553
    ISSN (online) 1949-2553
    DOI 10.18632/oncotarget.12070
    Database MEDical Literature Analysis and Retrieval System OnLINE

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