Search

Your search keyword '"Stuck, Boris A."' showing total 501 results
Start Over Author "Stuck, Boris A." Publication Year Range Last 10 years

Refine your results

more »

more »

more »

more »
501 results on '"Stuck, Boris A."'

14. Partial update of the German S3 Guideline Sleep-Related Breathing Disorders in Adults: AWMF Registry No. 063-001—German Sleep Society (Deutsche Gesellschaft für Schlafforschung und Schlafmedizin – DGSM)

Author

Stuck, Boris A., Arzt, Michael, Fietze, Ingo, Galetke, Wolfgang, Hein, Holger, Heiser, Clemens, Herkenrath, Simon D., Hofauer, Benedikt, Maurer, Joachim T., Mayer, Geert, Orth, Maritta, Penzel, Thomas, Randerath, Winfried, Sommer, J. Ulrich, Steffen, Armin, and Wiater, Alfred

Published
2022
Full Text
View/download PDF

19. The Role of TGF-β1 and Mutant SMAD4 on Epithelial-Mesenchymal Transition Features in Head and Neck Squamous Cell Carcinoma Cell Lines.

Author

Bette, Michael, Reinhardt, Laura, Gansukh, Uyanga, Xiang-Tischhauser, Li, Meskeh, Haifa, Di Fazio, Pietro, Buchholz, Malte, Stuck, Boris A., and Mandic, Robert

Subjects
SQUAMOUS cell carcinoma, FLOW cytometry, CARRIER proteins, EPITHELIAL-mesenchymal transition, HEAD & neck cancer, POLYMERASE chain reaction, CELL proliferation, CELL motility, CELL lines, KERATINOCYTES, IMMUNOHISTOCHEMISTRY, GENE expression, WESTERN immunoblotting, RECOMBINANT proteins, GENETIC mutation, TRANSFORMING growth factors-beta, SEQUENCE analysis
Abstract

Simple Summary: Head and neck squamous cell carcinomas (HNSCCs) represent more than 90% of all malignancies in the upper aero-digestive tract. Their ability to metastasize is tightly associated with the patient's survival. The process of epithelial–mesenchymal transition (EMT) is thought to be a central mechanism for invasion and metastasis. Here, we investigated the responsiveness of HNSCC cell lines and the HaCaT control cell line to the EMT master regulator TGF-β1 and observed major differences in the level of sensitivity to this cytokine. The more epithelial HNSCC cells and HaCaT control cells responded more extensively to TGF-β1 than the less epithelial HNSCC cells. Mutant SMAD4 was detected in the most mesenchymal HNSCC cell line and appears to contribute to mesenchymal features in HNSCC cells. These observations could help to explain the different histomorphological phenotypes of HNSCC tumors, which could be linked to the risk of metastatic spread. The aim of the present study was to investigate possible differences in the sensitivity of HNSCC cells to known EMT regulators. Three HNSCC cell lines (UM-SCC-1, -3, -22B) and the HaCaT control keratinocyte cell line were exposed to transforming growth factor beta 1 (TGF-β1), a known EMT master regulator, and the cellular response was evaluated by real-time cell analysis (RTCA), Western blot, quantitative PCR, flow cytometry, immunocytochemistry, and the wound closure (scratch) assay. Targeted sequencing on 50 cancer-related genes was performed using the Cancer Hotspot Panel v2. Mutant, and wild type SMAD4 cDNA was used to generate recombinant SMAD4 constructs for expression in mammalian cell lines. The most extensive response to TGF-β1, such as cell growth and migration, β-actin expression, or E-cadherin (CDH1) downregulation, was seen in cells with a more epithelial phenotype. Lower response correlated with higher basal p-TGFβ RII (Tyr424) levels, pointing to a possible autocrine pre-activation of these cell lines. Targeted sequencing revealed a homozygous SMAD4 mutation in the UM-SCC-22B cell line. Furthermore, PCR cloning of SMAD4 cDNA from the same cell line revealed an additional SMAD4 transcript with a 14 bp insertion mutation, which gives rise to a truncated SMAD4 protein. Overexpression of this mutant SMAD4 protein in the highly epithelial control cell line HaCaT resulted in upregulation of TGF-β1 and vimentin. Consistent with previous reports, the invasive and metastatic potential of HNSCC tumor cells appears associated with the level of autocrine secretion of EMT regulators such as TGF-β1, and it could be influenced by exogenous EMT cytokines such as those derived from immune cells of the tumor microenvironment. Furthermore, mutant SMAD4 appears to be a significant contributor to the mesenchymal transformation of HNSCC cells. [ABSTRACT FROM AUTHOR]

Published
2024
Full Text
View/download PDF

29. Evaluation of oxidative and glycolytic energy production in HPV positive and negative HNSCC cell lines after photon-based irradiation

Author

Mandic, Robert, additional, Bette, Michael, additional, San Lucas Zambrano, Jennifer S., additional, Al Rabadi, Hytham, additional, Neff, Andreas, additional, Stuck, Boris Alexander, additional, Theiß, Ulrike, additional, Vogt, Sebastian, additional, Meißner, Wolfgang, additional, and Kasahara, Norio, additional

Published
2024
Full Text
View/download PDF

48. Teil-Aktualisierung S3-Leitlinie Schlafbezogene Atmungsstörungen bei Erwachsenen: AWMF-Registernummer 063-001 – Deutsche Gesellschaft für Schlafforschung und Schlafmedizin (DGSM)

Author

Stuck, Boris A., Arzt, Michael, Fietze, Ingo, Galetke, Wolfgang, Hein, Holger, Heiser, Clemens, Herkenrath, Simon D., Hofauer, Benedikt, Maurer, Joachim T., Mayer, Geert, Orth, Maritta, Penzel, Thomas, Randerath, Winfried, Sommer, J. Ulrich, Steffen, Armin, and Wiater, Alfred

Published
2020
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results