Yohei Shida
Nagasaki University
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Publication
Featured researches published by Yohei Shida.
International Journal of Urology | 2018
Tomoaki Hakariya; Yohei Shida; Toshifumi Tsurusaki; Junichi Watanabe; Masataka Furukawa; Fukuzo Matsuya; Yasuyoshi Miyata; Hideki Sakai
To elucidate the effect of prior use of ethinylestradiol on enzalutamide treatment for men with castration‐resistant prostate cancer.
The Prostate | 2017
Akihiro Asai; Yasuyoshi Miyata; Tomohiro Matsuo; Yohei Shida; Tomoaki Hakariya; Kojiro Ohba; Hideki Sakai
The anti‐cancer mechanism of neo‐adjuvant hormonal therapy (NHT) is not well understood. Lymphangiogenesis plays an important role in cancer progression and is regulated by a complex mechanism that includes vascular endothelial growth factor (VEGF) signaling. However, there is little information regarding relationship between lymphangiogenesis and androgen deprivation. The aim of this study was to clarify changes in lymphangiogenesis and VEGF expression induced by androgen deprivation in prostate cancer in vivo and in vitro.
Clinical Case Reports | 2017
Yohei Shida; Tomoaki Hakariya; Yasuyoshi Miyata; Hideki Sakai
We report three cases of nonmetastatic prostate cancer treated effectively with long‐term primary intermittent androgen deprivation (IAD). IAD is not a standard therapy for patients with nonmetastatic prostate cancer. However, based on our experience, we suggest that IAD is one of useful therapeutic tools under certain patients’ condition.
Archive | 2016
Yasuyoshi Miyata; Yohei Shida; Tomohiro Matsuo; TomoakiHakariya; Hideki Sakai
Hormonal therapy is a major and effective tool in the treatment of prostate cancer patients. This is especially true for patients in the advanced stages of disease. Unfortunately, almost all prostate cancer cells will develop into castration‐resistant prostate cancer (CRPC) despite continued therapy and suppression of testosterone levels. Up until 5–6 years ago, there was little effective therapy for the treatment of CRPC patients. However, recently, a variety of methodologies and drugs such as cabazitaxel and sipuleucel‐T have been approved globally for the treatment of CRPC. Two novel drugs, abiraterone acetate and enzartamide, have also become available as potential treatment options. However, the anticancer effects of these two drugs are not always satisfactory in terms of prolonging survival. These drugs are also associated with adverse events and are expensive when compared with the costs of previously used anticancer drugs. In this section, we pay particular attention to hormonal therapies that do not include the use of abiraterone acetate or enzartamide. We believe that a detailed understanding of the range of currently available hormonal therapies, including their associated benefits and limitations, is important for supporting the prolongation of survival in patients with advanced prostate cancer. Therefore, this section offers a valuable discussion on the treatment strategies for prostate cancer including CRPC.
Biochemical and Biophysical Research Communications | 2007
Yohei Shida; Tsukasa Igawa; Tomoaki Hakariya; Hideki Sakai; Hiroshi Kanetake
Biochemical and Biophysical Research Communications | 2006
Tomoaki Hakariya; Yohei Shida; Hideki Sakai; Hiroshi Kanetake; Tsukasa Igawa
International Journal of Clinical and Experimental Pathology | 2014
Kojiro Ohba; Yasuyoshi Miyata; Tomohiro Matsuo; Akihiro Asai; Kensuke Mitsunari; Yohei Shida; Shigeru Kanda; Hideki Sakai
Translational Research | 2016
Kensuke Mitsunari; Yasuyoshi Miyata; Akihiro Asai; Tomohiro Matsuo; Yohei Shida; Tomoaki Hakariya; Hideki Sakai
BMC Research Notes | 2015
Yohei Shida; Tsukasa Igawa; Kuniko Abe; Tomoaki Hakariya; Kousuke Takehara; Toru Onita; Hideki Sakai
Anticancer Research | 2016
Yohei Shida; Tomoaki Hakariya; Kosuke Takehara; Toru Onita; Yasuyoshi Miyata; Hideki Sakai