Maiko Tanaka
Hiroshima University
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Publication
Featured researches published by Maiko Tanaka.
Biosensors and Bioelectronics | 2008
Maiko Tanaka; Tomoko Tsutsui; Yuhki Yanase; Hidenori Suzuki; Michihiro Hide
Surface plasmon resonance (SPR) biosensors detect large changes of angle of resonance (AR) when RBL-2H3 mast cells are cultured on a sensor chip and stimulated with antigen. However, the detail of molecular events that are responsible for such large changes of AR remained unknown. In this study, we investigated the relationship between intracellular signaling events induced by antigen and the change of AR, by genetic manipulation of intracellular signaling molecules; spleen tyrosine kinase (Syk), src-like adaptor protein (SLAP), linker for activation of T cells (LAT), growth-factor-receptor-bound protein 2 (Grb2), Grb2-related adaptor protein (Gads), and isotypes of protein kinase C (PKC). RBL-2H3 mast cells overexpressing dominant-negative Syk or SLAP, which both interfere with active Syk, exhibited only minimal increase of AR in response to antigen stimulation. Likewise, the interference of the activation of LAT and Gads, by expressing dominant-negative LAT and Gads, respectively, resulted in nearly complete suppression of the antigen-induced increase of AR. The cells overexpressing PKCs, apart from PKCbeta, showed a reduced extent of increase of AR in response to antigen stimulation. Moreover, the introduction of the small interfering RNA targeted against PKCbeta suppressed the antigen-induced increase of AR. These results indicate that the activation of Syk, LAT, Gads, and subsequent PKCbeta is indispensable for the antigen-induced increase of AR of mast cells detected by SPR biosensors.
Surgery Today | 2013
Seiichi Shimizu; Akihiko Oshita; Hirotaka Tashiro; Hironobu Amano; Tsuyoshi Kobayashi; Maiko Tanaka; Koji Arihiro; Hideki Ohdan
A 76-year-old male was referred for the treatment of liver tumors detected by abdominal computed tomography (CT). Dynamic CT revealed a low-density tumor with an irregularly enhanced rim in the left lateral sector, and a highly enhanced, well-circumscribed tumor in the caudate lobe, accompanied by dilation of the intrahepatic biliary ducts in the left lobe. Preoperative imaging studies led to the diagnosis of double cancers consisting of intrahepatic cholangiocarcinoma and hepatocellular carcinoma (HCC). Left hemihepatectomy with caudate lobectomy was performed. The postoperative course was uneventful. Microscopic evaluation revealed that the tumor in the left lateral sector was adenosquamous carcinoma (ASC), whereas that in the caudate lobe was HCC. This report presents the first case describing the resection of synchronous double cancers of primary hepatic ASC and HCC.
Journal of Cutaneous Pathology | 2016
Boštjan Luzar; Maiko Tanaka; Johann W. Schneider; Eduardo Calonje
Microcystic/ reticular schwannoma is exceptionally rare yet distinctive morphological variant of schwannoma with predilection for visceral sites lacking association with neurofibromatosis.
Case Reports in Oncology | 2016
Yui Hattori; Kazuhiro Sentani; Takuya Hattori; Yoshimi Matsuo; Mikio Kawai; Hajime Shindo; Maiko Tanaka; Michihiro Hide; Wataru Yasui
Balloon cell malignant melanoma (BCMM) is a very rare malignant melanoma subtype. The clinical appearance of BCMM varies; it may be nodular, ulcerated, polypoid, papillomatous and often non-pigmented. The tumor cells histologically appear large, polygonal or round and contain abundant granular or vacuolated cytoplasm. We herein report the case of a 32-year-old female who presented with a focal eccentric pigmented mass in the left lumbar region of 15 mm in diameter that had been present for several years. She underwent tumor excision. The histopathological analysis showed epithelioid melanocytes with clear cytoplasm. An immunohistochemical analysis revealed that the cells were positive for HMB-45 and S-100 protein and negative for cytokeratin. The balloon cell component stained negative for Fontana-Masson. A month later, the patient underwent excision of the bilateral inguinal lymph nodes and metastatic BCMM was revealed. The lymph node metastases showed the complete replacement of lymph nodes by balloon cells. A diagnosis of BCMM (Breslow depth 10 mm, Clark level V) without ulcer was rendered. Staining with Ki-67 was positive in almost 44% of the balloon cells.
Biochemistry and biophysics reports | 2016
Yuuka Shibata; Tomoharu Yokooji; Ryo Itamura; Yumeka Sagara; Takanori Taogoshi; Katsunari Ogawa; Maiko Tanaka; Michihiro Hide; Kenji Kihira; Hiroaki Matsuo
Inadvertent leakage of medications with vesicant properties can cause severe necrosis in tissue, which can have devastating long-term consequences. The aim of this study was to evaluate the extent of extravasation injury induced by thiopental and propofol, and the effects of cooling or warming of local tissue on extravasation injury at macroscopic and histopathologic levels. Rats were administered intradermally thiopental (2.5 mg/100 µL) or propofol (1.0 mg/100 µL). Rats were assigned randomly to three groups: control (no treatment), cooling and warming. Local cooling (18–20 °C) or warming (40–42 °C) was applied for 3 h immediately after agent injection. Lesion sizes (erythema, induration, ulceration, necrosis) were monitored after agent injection. Histopathology was evaluated in skin biopsies taken 24 h after agent injection. Thiopental injection induced severe skin injury with necrosis. Peak lesions developed within 24 h and healed gradually 18–27 days after extravasation. Propofol induced inflammation but no ulceration, and lesions healed within 1–2 days. Local cooling reduced thiopental- and propofol-induced extravasation injuries but warming strongly exacerbated the skin lesions (e.g., degeneration, necrosis) induced by extravasation of thiopental and propofol. Thiopental can be classified as a “vesicant” that causes tissue necrosis and propofol can be classified as an “irritant”. Local cooling protects (at least in part) against skin disorders induced by thiopental and propofol, whereas warming is harmful.
Journal of The American Academy of Dermatology | 2012
Joya Pawade; Maiko Tanaka; Stephen Morris; Tracey Mitchell; Fiona Child; Mary Wain; Sean Whittaker; Alistair Robson
Internal Medicine | 2014
Hiroshi Oiwa; Keichiro Mihara; Takanobu Kan; Maiko Tanaka; Hajime Shindo; Kazuhiko Kumagai; Eiji Sugiyama
Experimental and Therapeutic Medicine | 2010
Koji Arihiro; Miyo Oda; Katsunari Ogawa; Kenshi Tominaga; Yoshie Kaneko; Tomomi Shimizu; Shiho Ohnishi; Megumi Oda; Yuki Kurita; Yuko Taira; Masayoshi Fujii; Maiko Tanaka
Journal of Cutaneous Immunology and Allergy | 2018
Masaya Moriwaki; Akio Tanaka; Maiko Tanaka; Shunsuke Takahagi; Michihiro Hide
Biological & Pharmaceutical Bulletin | 2018
Yuuka Shibata; Yumeka Sagara; Tomoharu Yokooji; Takanori Taogoshi; Maiko Tanaka; Michihiro Hide; Hiroaki Matsuo