Takeshi Yanagishita
Aichi Medical University
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Publication
Featured researches published by Takeshi Yanagishita.
Journal of Dermatological Science | 2010
Yuichiro Ohshima; Ichiro Yajima; Mayuko Y. Kumasaka; Takeshi Yanagishita; Daisuke Watanabe; Masahide Takahashi; Yuji Inoue; Hironobu Ihn; Yoshinari Matsumoto; Masashi Kato
Yoshiki Tokura Department of Dermatology, University of Occupational and Environmental Health, 1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu 807-8555, Japan *Corresponding author at: Department of Dermatology, Kyoto University Graduate School of Medicine, 54 Shogoin-Kawara, Sakyo, Kyoto 606-8507, Japan. Tel.: +81 75 7513310/93 6917445; fax: +81 75 7613002/93 6910907 E-mail address: [email protected] (Kenji Kabashima).
British Journal of Dermatology | 2013
Yuichiro Ohshima; Takeshi Yanagishita; Keiko Ito; Yasuhiko Tamada; Naoki Nishimura; Yoko Inukai; Satoshi Iwase; Junichi Sugenoya; Daisuke Watanabe
1 Davies H, Bignell GR, Cox C et al. Mutations of the BRAF gene in human cancer. Nature 2002; 417:949–54. 2 Long GV, Menzies AM, Nagrial A et al. Clinico-pathologic correlates of BRAF mutation status in 207 consecutive patients with metastatic melanoma. J Clin Oncol 2010; 28:15S (suppl.; abstr. 8548) presented at the ASCO Annual Meeting, 4–8 June 2010, Chicago, IL, U.S.A. 3 Jakob JA, Bassett RL, Ng CS et al. Clinical characteristics and outcomes associated with BRAF and NRAS mutations in metastatic melanoma. J Clin Oncol 2011; 29(suppl.; abstr. 8500) presented at the ASCO Annual Meeting, 3–7 June 2011, Chicago, IL, U.S.A. 4 Dienstmann R, Tabernero J. BRAF as a target for cancer therapy. Anticancer Agents Med Chem 2011; 11:285–95. 5 Chapman PB, Hauschild A, Robert C et al. Improved survival with vemurafenib in melanoma with BRAF V600E mutation. N Engl J Med 2011; 364:2507–16. 6 U.S. Food and Drug Administration News Release. Available at: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ ucm268241.htm (last accessed 2 July 2012). 7 Infante JR, Falchook GS, Lawrence DP et al. Phase I ⁄ II study to assess safety, pharmacokinetics, and efficacy of the oral MEK 1 ⁄2 inhibitor GSK 1120212 (GSK212) dosed in combination with the oral BRAF inhibitor GSK 2118436 (GSK 436). J Clin Oncol 2011; 29 (suppl.; abstr. CRA8503) presented at the ASCO Annual Meeting, 3–7 June 2011, Chicago, IL, U.S.A. 8 Benlloch S, Paya A, Alenda C et al. Detection of BRAF V600E mutation in colorectal cancer. Comparison of automatic sequencing and real-time chemistry methodology. J Mol Diagn 2006; 8:540–3. 9 Pichler M, Balic M, Stadelmeyer E et al. Evaluation of high-resolution melting analysis as a diagnostic tool to detect the BRAF V600E mutation in colorectal tumors. J Mol Diagn 2009; 11:140–7. 10 Carbonell P, Turpin MC, Torres-Moreno D et al. Comparison of allelic discrimination by dHPLC, HRM, and TaqMan in the detection of BRAF mutation V600E. J Mol Diagn 2011; 13:467–73. 11 Fusi A, Berdel R, Havemann S et al. Enhanced detection of BRAFmutants by pre-PCR cleavage of wild-type sequences revealed circulating melanoma cells heterogeneity. Eur J Cancer 2011; 47:1971– 6. 12 Houben R, Becker JC, Kappel A et al. Constitutive activation of the Ras-Raf signalling pathway in metastatic melanoma is associated with poor prognosis. J Carcinog 2004; 3:6. 13 Yancovitz M, Litterman A, Yoon J et al. Intraand inter-tumor heterogeneity of BRAF (V600E) mutations in primary and metastatic melanoma. PLoS ONE 2012; 7:e29336.
PLOS ONE | 2011
Nguyen Dinh Thang; Ichiro Yajima; Mayuko Y. Kumasaka; Shoko Ohnuma; Takeshi Yanagishita; Rumiko Hayashi; Hossain Uddin Shekhar; Daisuke Watanabe; Masashi Kato
Explosive increases in skin cancers have been reported in more than 36 million patients with arsenicosis caused by drinking arsenic-polluted well water. This study and previous studies showed high levels of barium as well as arsenic in the well water. However, there have been no reports showing a correlation between barium and cancer. In this study, we examined whether barium (BaCl2) may independently have cancer-related effects on human precancerous keratinocytes (HaCaT). Barium (5–50 µM) biologically promoted anchorage-independent growth and invasion of HaCaT cells in vitro. Barium (5 µM) biochemically enhanced activities of c-SRC, FAK, ERK and MT1-MMP molecules, which regulate anchorage-independent growth and/or invasion. A SRC kinase specific inhibitor, protein phosphatase 2 (PP2), blocked barium-mediated promotion of anchorage-independent growth and invasion with decreased c-SRC kinase activity. Barium (2.5–5 µM) also promoted anchorage-independent growth and invasion of fibroblasts (NIH3T3) and immortalized nontumorigenic melanocytes (melan-a), but not transformed cutaneous squamous cell carcinoma (HSC5 and A431) and malignant melanoma (Mel-ret) cells, with activation of c-SRC kinase. Taken together, our biological and biochemical findings newly suggest that the levels of barium shown in drinking well water independently has the cancer-promoting effects on precancerous keratinocytes, fibroblast and melanocytes in vitro.
Photodermatology, Photoimmunology and Photomedicine | 2009
Aki Nakano; Yasuhiko Tamada; Daisuke Watanabe; Natsuko Ishida; Noriko Yamashita; Tomoe Kuhara; Takeshi Yanagishita; Chiharu Kawamura; Yoichi Akita; Yoshinari Matsumoto
Background/purpose: Topical 5‐aminolevulinic acid (ALA)‐based photodynamic therapy (PDT) is effective for actinic keratosis (AK); few studies have examined Oriental patients. The aim of this study is to assess the efficacy of PDT for the treatment of Japanese AK patients classified by lesion size and histological severity.
Journal of Dermatology | 2008
Noriko Yamashita; Hirokazu Shimizu; Morihiro Kawada; Takeshi Yanagishita; Daisuke Watanabe; Yasuhiko Tamada; Yoshinari Matsumoto
Botulinum toxin A is widely used in Europe and the USA for the treatment of localized hyperhidrosis, and its efficacy has been recognized. In this study, botulinum toxin A (Botox) was locally injected at 30 sites (2 U/injection) on the right palm in 27 patients with palmar hyperhidrosis (14 severe patients, 13 mild patients), and the results confirmed the efficacy of injection. The amount of sweat was then quantified for the left and right hands every month after local injection. The quantity of sweat on the treated hand was approximately one‐fifth that on the untreated hand. In addition, the quantity of sweat on the untreated hand decreased slightly. Over time, the quantity of sweat on the treated hand increased slightly, but the quantity of sweat on the treated hand at 6 months after injection was less than half that before injection, and there were significant differences before and after injection. In the present study, severe sweating was defined as 1 mg/cm2/min or more and mild sweating as less than 1 mg/cm2/min, and the therapeutic effects of botulinum toxin A were analyzed in relation to severity. When compared to the mild cases, the quantity of sweat remained higher in the severe cases after botulinum toxin A therapy. Therefore, to achieve satisfactory effects in severe cases, it would be necessary to increase the number of injection sites, as well as injection dose.
Journal of Dermatological Science | 2009
Ichiro Yajima; Mayuko Y. Kumasaka; Nguyen Dinh Thang; Takeshi Yanagishita; Nobutaka Ohgami; David M. Kallenberg; Yuji Naito; Toshikazu Yoshikawa; Naomi Sakashita; Masashi Kato
Since melanoma is an aggressive cancer with highly metastatic ability, the increase in its incidence is a threat to public health. Therefore, it is important to find new biomarkers and effective therapies. The c-RET proto-oncogene encodes a receptor-tyrosine kinase, and glial cell line-derived neurotrophic factor (GDNF)related ligands, including GDNF, neurturin, artemin and persephin, have been reported to be ligands of RET [1]. RFP-RET is a hybrid oncogene between c-RET and RFP, and its kinase activity is highly up-regulated compared with the activity of c-RET tyrosine kinase [2]. Previously, we established a metallothionein-I/RFP-RETtransgenic mouse of line 304/B6 (RET-mice) [3], in which systemic skin melanosis, benign melanocytic tumor(s) and malignant melanoma stepwise develop [4]. The transgenic mouse line is a powerful tool for analyzing the effects of molecules on melanomagenesis. In fact, we performed DNA microarray analysis for
Journal of Dermatology | 2011
Keiko Ito; Takeshi Yanagishita; Yuichiro Ohshima; Yasuhiko Tamada; Daisuke Watanabe
A dose of 60 units (U) of botulinum toxin type A (BT‐A) has been confirmed to have efficacy for patients with palmoplantar hyperhidrosis. However, the effectiveness of this dose is limited in severe cases defined as sweat production of 2 mg/cm2 per min or more (measured by the ventilated capsule method) and a Hyperhidrosis Disease Severity Scale (HDSS) grade of 3 or 4. An increased dose of 90 U of BT‐A was found to reduce sweating for approximately 7 months. In a comparison of patients with sweat production of more than 2.5 mg/cm2 per min and an HDSS grade of 4 and patients with sweat production of 2.5 mg/cm2 per min or less and an HDSS grade of 3, there was no difference in the reduction of sweat production at 5 months, but the duration of the reduced sweating was shorter for the former group. This suggests that there are limits to the efficacy of BT‐A for severe forms of the disease with sweat production of more than 2.5 mg/cm2 per mL.
Journal of Dermatological Science | 2012
Takeshi Yanagishita; Yasuhiko Tamada; Yuichiro Ohshima; Keiko Ito; Yoichi Akita; Daisuke Watanabe
Primary or secondary hyperhidrosis is excessive sweating beyond that required for returning body temperature to normal. It can be focal or generalized and commonly affects the underarms, Al specific binding fluorescence reagent and we investigated the mechanism of the antiperspirant action of AC. Palmar hyperhidorosis patients (n = 127) were topically treated with 20% AC solution without occlusion once a day for 1 month. Collection of subjects from patients was based on informed consent and declaration of Helsinki principles received approval of the ethical committee in Aichi Medical University School of Medicine (No. 11-014). First, sweat production was measured by palms, soles or face [1]. The disease often significantly affects the patient’s quality of life. Treatment options include topical aluminum chloride (AC), iontophoresis, botulinum toxin A, oral anticholinergics, and endoscopic sympathectomy. Topical AC is a well-established therapy for hyperhidrosis and is the first-line therapy for mild to moderate disease [2]. The mechanism of the action of aluminum (Al) salt in the forearm or axilla has been investigated in a few studies [3,4]. However, there has been no report on the mechanism of the antiperspirant action of AC for treatment of palmoplantar hyperhidrosis. In this study, we investigated the histological localization of Al for palmar hyperhidorosis by using an
British Journal of Dermatology | 2014
Takeshi Yanagishita; Kazumitsu Sugiura; Yoshiyuki Kawamoto; Keiko Ito; Yuki Marubashi; Nobuhiko Taguchi; Masashi Akiyama; Daisuke Watanabe
DEAR EDITOR, Bj€ ornstad syndrome (OMIM 262000) is an autosomal recessive condition characterized by sensorineural deafness and pili torti. Only 39 cases of Bj€ ornstad syndrome have been reported in the English literature and only two cases have been reported in Japan. Thus, the syndrome is an extremely rare inherited disorder. Herein we present a case of Bj€ ornstad syndrome in which novel mutations in the BCS1L gene were identified. A Japanese female aged 2 years and 3 months with no family history of hair and auditory symptoms (Fig. 1a) presented with a 2-year history of sparse hair on the head. Retarded speech development was revealed by medical examination, and a diagnosis of severe sensorineural deafness by auditory brainstem response (ABR) was made by otolaryngology. Physical examination revealed that her scalp hairs were thin and sparse with differing lengths (Fig. 1b, c). Clinical examinations of the skin, mucosae, nails, eyes and teeth revealed no abnormalities. Routine laboratory data
Clinical and Experimental Dermatology | 2009
Natsuko Ishida; Daisuke Watanabe; Yoichi Akita; Aki Nakano; Noriko Yamashita; Tomoe Kuhara; Takeshi Yanagishita; Tomohiro Takeo; Yasuhiko Tamada; Yoshinari Matsumoto
Background. Photodynamic therapy (PDT) with 5‐aminolaevulinic acid (5‐ALA) is a noninvasive and effective treatment for superficial skin cancers. Etretinate, a derivate of vitamin A, with the chemical formula ethyl(2E,4E,6E,8E)‐9‐(4‐methoxy‐2,3,6‐trimethylphenyl)‐3,7‐dimethyl‐2,4,6,8‐nona‐tetraenoate, has been reported to have antitumour effects and to regulate the proliferation and differentiation of skin cancers.