22 research outputs found
Full-Length L1CAM and Not Its Δ2Δ27 Splice Variant Promotes Metastasis through Induction of Gelatinase Expression
Tumour-specific splicing is known to contribute to cancer progression. In the case of the L1 cell adhesion molecule (L1CAM), which is expressed in many human tumours and often linked to bad prognosis, alternative splicing results in a full-length form (FL-L1CAM) and a splice variant lacking exons 2 and 27 (SV-L1CAM). It has not been elucidated so far whether SV-L1CAM, classically considered as tumour-associated, or whether FL-L1CAM is the metastasis-promoting isoform. Here, we show that both variants were expressed in human ovarian carcinoma and that exposure of tumour cells to pro-metastatic factors led to an exclusive increase of FL-L1CAM expression. Selective overexpression of one isoform in different tumour cells revealed that only FL-L1CAM promoted experimental lung and/or liver metastasis in mice. In addition, metastasis formation upon up-regulation of FL-L1CAM correlated with increased invasive potential and elevated Matrix metalloproteinase (MMP)-2 and -9 expression and activity in vitro as well as enhanced gelatinolytic activity in vivo. In conclusion, we identified FL-L1CAM as the metastasis-promoting isoform, thereby exemplifying that high expression of a so-called tumour-associated variant, here SV-L1CAM, is not per se equivalent to a decisive role of this isoform in tumour progression
Moderne EDV-Anwendungen zur Verkehrsbeeinflussung: Referate der SVI/IVT-Tagung vom 3. März 1989
Beherrschung kritischer Reaktionen in Mehrphasensystemen durch technische Massnahmen. T. 2: Zur sicherheitstechnischen Beurteilung von Semibatch-Prozessen mit Gas/Fluessigkeits-Systemen Abschlussbericht
In this project physical and process technological basics for the removal of scale layers on austenitic steels with CO_2-laser radiation have been worked out. Scales from hot rolling (15 #mu#m thickness) and TIG welding seams (1 #mu#m thickness) have been investigated. The most important results can be summarized as follows: A complete descaling is possible both with pulsed and continuous wave CO_2-laser radiation in case of an appropriate process management, the feed rate is approximately 9.5 cm"2/s for a laser power of 1600 W, the pitting potential as a measure for the corrosion resistance for the laser treated samples can be compared with that of pickled samples, the improved corrosion resistance results from the complete removal of the scale layers, the dissolution of the chromium carbides at the grain boundaries and from the formation of chromium oxides at the surface. The new technology is a promising alternative regarding processing quality and economic efficiency in dependence on the application. (orig.)Available from TIB Hannover: F96B1924+a / FIZ - Fachinformationszzentrum Karlsruhe / TIB - Technische InformationsbibliothekSIGLEBundesministerium fuer Bildung, Wissenschaft, Forschung und Technologie, Bonn (Germany)DEGerman
Wärmeübergang und Druckverlust wässeriger Tensidlösungen an einer querangeströmten berippten Rohrwendel
DOCK8 Deletions and Mutations Are Associated With The Autosomal Recessive Hyper-IgE Phenotype
Genetic evidence for <em>PLASMINOGEN</em> as a shared genetic risk factor of coronary artery disease and periodontitis
Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome
BACKGROUND: The genetic etiologies of the hyper-IgE syndromes are diverse. Approximately 60% to 70% of patients with hyper-IgE syndrome have dominant mutations in STAT3, and a single patient was reported to have a homozygous TYK2 mutation. In the remaining patients with hyper-IgE syndrome, the genetic etiology has not yet been identified. OBJECTIVES: We aimed to identify a gene that is mutated or deleted in autosomal recessive hyper-IgE syndrome. METHODS: We performed genome-wide single nucleotide polymorphism analysis for 9 patients with autosomal-recessive hyper-IgE syndrome to locate copy number variations and homozygous haplotypes. Homozygosity mapping was performed with 12 patients from 7 additional families. The candidate gene was analyzed by genomic and cDNA sequencing to identify causative alleles in a total of 27 patients with autosomal-recessive hyper-IgE syndrome. RESULTS: Subtelomeric biallelic microdeletions were identified in 5 patients at the terminus of chromosome 9p. In all 5 patients, the deleted interval involved dedicator of cytokinesis 8 (DOCK8), encoding a protein implicated in the regulation of the actin cytoskeleton. Sequencing of patients without large deletions revealed 16 patients from 9 unrelated families with distinct homozygous mutations in DOCK8 causing premature termination, frameshift, splice site disruption, and single exon deletions and microdeletions. DOCK8 deficiency was associated with impaired activation of CD4+ and CD8+T cells. CONCLUSION: Autosomal-recessive mutations in DOCK8 are responsible for many, although not all, cases of autosomal-recessive hyper-IgE syndrome. DOCK8 disruption is associated with a phenotype of severe cellular immunodeficiency characterized by susceptibility to viral infections, atopic eczema, defective T-cell activation and T(h)17 cell differentiation, and impaired eosinophil homeostasis and dysregulation of IgE