Publications by authors named "Motoi Tanabe"

Article Synopsis
  • - The study explores a new treatment for antibody-mediated rejection (AMR) in transplants using a lipid nanoparticle formulation of small-interfering RNA (siRNA) designed to target complement C5, which plays a crucial role in graft injury.
  • - In experiments with sensitized Lewis rats undergoing kidney transplants, the C5 siRNA-LNP effectively suppressed complement activity and significantly improved graft survival when combined with immunosuppressants cyclosporin (CsA) and deoxyspergualin (DSG).
  • - Results showed that using C5 siRNA-LNP led to a notable reduction in complement C5 expression and graft damage, suggesting this approach could be a promising strategy for preventing AMR in
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Next-generation sequencing (NGS) of tumor tissue (ie, clinical sequencing) can guide clinical management by providing information about actionable gene aberrations that have diagnostic and therapeutic significance. Here, we undertook a hospital-based prospective study (TOP-GEAR project, 2nd stage) to investigate the feasibility and utility of NGS-based analysis of 114 cancer-associated genes (the NCC Oncopanel test). We examined 230 cases (comprising more than 30 tumor types) of advanced solid tumors, all of which were matched with nontumor samples.

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Recently, a new entity "myoepithelioma-like tumor of the vulvar region (MELTVR)" was proposed as a rare mesenchymal neoplasm arising in vulvar regions of adult women. While MELTVRs morphologically resemble soft tissue myoepitheliomas and extraskeletal myxoid chondrosarcomas, they have a unique immunohistochemical profile (positive for epithelial membrane antigen and estrogen receptor, negative for S100 protein and glial fibrillary acidic protein, and loss of INI1/SMARCB1 expression), and lack EWSR1 and NR4A3 gene rearrangement, as seen by fluorescence in situ hybridization. MELTVRs are usually well-demarcated tumors, with no reports of extensive infiltrative growth.

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