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Regeneration of rat corpora cavernosa tissue by transplantation of CD133+ cells derived from human bone marrow and placement of biodegradable gel sponge sheet
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作者 Shogo Inoue Katsutoshi Miyamoto +5 位作者 Shunsuke Shinmei Koichi Shoji jun teishima Kazuhiro Sentani Wataru Yasui Akio Matsubara 《Asian Journal of Andrology》 SCIE CAS CSCD 2017年第2期203-207,共5页
The objective is to develop an easier technique for regenerating corpora cavernosa tissue through transplantation of human bone marrow-derived CD133+ cells into a rat corpora cavernosa defect model. We excised 2 mm&#... The objective is to develop an easier technique for regenerating corpora cavernosa tissue through transplantation of human bone marrow-derived CD133+ cells into a rat corpora cavernosa defect model. We excised 2 mm× 2 mm squares of the right corpora cavernosa of twenty-three 8-week-old male nude rats. AIginate gel sponge sheets supplemented with 1 × 10^4 CD133+ cells were then placed over the excised area of nine rats. Functional and histological evaluations were carried out 8 weeks later. The mean intracavernous pressure/mean arterial pressure ratio for the nine rats (0.34258 ± 0.0831) was significantly higher than that for eight rats with only the excision (0.0580±0.0831, P = 0.0238) and similar to that for five rats for which the penis was exposed, and there was no excision (0.37228±0.1051, P = 0.8266). Immunohistochemical analysis revealed that the nine fully treated rats had venous sinus-like structures and quantitative reverse transcription polymerase chain reaction analysis of extracts from their alginate gel sponge sheets revealed that the amounts of mRNA encoding the nerve growth factor (NGF), and vascular endothelial growth factor (VEGF) were significantly higher than those for rats treated with alginate gel sheets without cell supplementation (NGF: P= 0.0309; VEGF: P〈 0.0001). These findings show that transplantation of CD133+ cells accelerates functional and histological recovery in the corpora cavernosa defect model. 展开更多
关键词 alginate gel sponge sheet CD133+ cell corpora cavernosa
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Role of circulating tumor cell clusters in patients with metastatic hormone-sensitive prostate cancer receiving a gonadotropin-releasing hormone antagonist: A pilot study
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作者 Yuki Kohada Hiroki Kusumoto +10 位作者 Takashi Kukimoto Jotaro Mikami jun Ito Katsutoshi Asano Toru Yaegashi Kanichi Nakagawara jun teishima Yasuhiro Kaiho Nobuyuki Hinata Yasuhiro Nakamura Makoto Sato 《Asian Journal of Urology》 CSCD 2023年第2期210-212,共3页
Dear Editor,Prostate cancer is the most common cancer among men[1].Androgen deprivation therapy(ADT)has remained the primary treatment of metastatic-hormone-sensitive prostate cancer(mHSPC),providing a temporary disea... Dear Editor,Prostate cancer is the most common cancer among men[1].Androgen deprivation therapy(ADT)has remained the primary treatment of metastatic-hormone-sensitive prostate cancer(mHSPC),providing a temporary disease control in the majority of patients.Despite initial ADT response,castration-resistance prostate cancer(CRPC)still develops.Previous study have attempted to determine possible biomarkers for poor prognosis in patients with CRPC[2]. 展开更多
关键词 PATIENTS METASTATIC cancer
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Molecular mechanisms of docetaxel resistance in prostate cancer 被引量:1
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作者 Yohei Sekino jun teishima 《Cancer Drug Resistance》 2020年第4期676-685,共10页
Docetaxel(DTX)chemotherapy offers excellent initial response and confers significant survival benefit in patients with castration-resistant prostate cancer(CRPC).However,the clinical utility of DTX is compromised when... Docetaxel(DTX)chemotherapy offers excellent initial response and confers significant survival benefit in patients with castration-resistant prostate cancer(CRPC).However,the clinical utility of DTX is compromised when primary and acquired resistance are encountered.Therefore,a more thorough understanding of DTX resistance mechanisms may potentially improve survival in patients with CRPC.This review focuses on DTX and discusses its mechanisms of resistance.We outline the involvement of tubulin alterations,androgen receptor(AR)signaling/AR variants,ERG rearrangements,drug efflux/influx,cancer stem cells,centrosome clustering,and phosphoinositide 3-kinase/AKT signaling in mediating DTX resistance.Furthermore,potential biomarkers for DTX treatment and therapeutic strategies to circumvent DTX resistance are reviewed. 展开更多
关键词 Prostate cancer DOCETAXEL drug resistant cancer BIOMARKER
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Significance of timing of therapeutic line on effectiveness of nivolumab for metastatic renal cell carcinoma
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作者 jun teishima Daiki Murata +12 位作者 Kazuma Yukihiro Yohei Sekino Shogo Inoue Tetsutaro Hayashi Koji Mita Yasuhisa Hasegawa Masao Kato Mitsuru Kajiwara Masanobu Shigeta Satoshi Maruyama Hiroyuki Moriyama Seiji Fujiwara Akio Matsubara 《Current Urology》 2023年第1期52-57,共6页
Objectives:This study aimed to clarify the significance of therapeutic timing on the effectiveness of nivolumab for treating metastatic renal cell carcinoma.Marterials and methods:Fifty-eight patients with metastatic ... Objectives:This study aimed to clarify the significance of therapeutic timing on the effectiveness of nivolumab for treating metastatic renal cell carcinoma.Marterials and methods:Fifty-eight patients with metastatic renal cell carcinoma treated with nivolumab monotherapy were retrospectively studied.Patients who were treated with nivolumab as second-line therapy were included in the second-line group,while the others were included in the later-line group.The clinicopathological characteristics,effects of nivolumab,and prognoses of these groups were compared.Results:Twenty and thirty-eight patients were included in the second-line and later-line groups,respectively.There were no significant differences in the distribution of International Metastatic Renal Cell Carcinoma Database Consotium risk and other clinicopathological characteristics between the 2 groups.The proportion of patients whose objective best response was progressive disease in the second-line group was significantly lower than that in the later-line group(15%vs.50%,p=0.0090).The 50%progression-free survival with nivolumab in the second-line group was significantly better than that in the later-line group(not reached and 5 months,p=0.0018).Multivariate analysis showed that the second-line setting was an independent predictive factor for better progression-free survival(p=0.0028,hazard ratio=0.108).The 50%overall survival after starting nivolumab in the second-line and later-line groups was not reached and 27.8 months,respectively(p=0.2652).Conclusions:The therapeutic efficacy of nivolumab as second-line therapy is expected to be better than that of later therapy. 展开更多
关键词 Immune checkpoint inhibitor Metastatic renal cell carcinoma Nivolumab Prognostic factor Second-line treatment
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