Correlation of clinical data and polymorphism for αィイD21aィエD2-adrenoceptor subtypes gene in Japanese patients with benign prostatic hypertrophy
Correlation of clinical data and polymorphism for αィイD21aィエD2-adrenoceptor subtypes gene in Japanese patients with benign prostatic hypertrophy
批准号:
09671608
负责人:
MORIYAMA Nobuo
金额:
$2.3万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1997
资助国家:
日本
项目状态:
已结题
起止时间:
1997 至 1998
中文摘要
One ofαI D 21 a I D 2-adrenoceptor subtypes,αI D 21 a I D 2-adrenoceptor is implicated in the pathophysiology of benign prostatic hypertrophy(BPH)。We examined polymorphism of the human ala-AR gene(Arg492to Cys)in 222BPH patients。There was no significant association ofαI D21a文件D2-adrenoceptor polymorphism with clinical(onset and degree of symptoms,size of BPH and response toα锡D21a文件D2-adrenoceptor blocker)and laboratory data(cholesterol and other lipid data,prostatic specific antigen,testosterone level)of the patient with BPH;however,the allele frequency in Japan was markedly different from US populs.The results did support the idea that BPH is associated with alterations inαI D21a THE D2-adrenoceptor gene.
英文摘要
One of αィイD21aィエD2-adrenoceptor subtypes ,αィイD21aィエD2-adrenoceptor is implicated in the pathophysiology of benign prostatic hypertrophy (BPH). We examined polymorphism of the human ala-AR gene (Arg492 to Cys) in 222 BPH patients. There was no significant association of αィイD21aィエD2-adrenoceptor polymorphism with clinical (onset and degree of symptoms, size of BPH and response to αィイD21aィエD2-adrenoceptor blocker) and laboratory data (cholesterol and other lipid data, prostatic specific antigen, testosterone level) of the patient with BPH ; however, the allele frequency in Japan was markedly different from US populations. The results did support the idea that BPH is associated with alterations in αィイD21aィエD2-adrenoceptor gene.
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Moriyama,N.,et al.: "Semiquantitative evaluation of α_<1a>-adrenoceptor subtype mRNA in human hypertrophied and non-hypertrophied prostates:regional comparison"LIFE SCIENCES. 64. 201-210 (1998)
Moriyama,N.等人:“人肥大和非肥大前列腺中α_1a-肾上腺素受体亚型mRNA的半定量评估:区域比较”LIFE SCIENCES 64. 201-210(1998)。
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Taniguchi,N., Ukai,Y., Kimura,K., Tanaka,T., Yano,J., Moriyama,N., et al.: "Identification of α_1-adrenoceptor subtypes in the human prostatic urethra." Naunyn Schmiedeberg's Arch.Pharmacol.355. 412-416 (1997)
Taniguchi, N.、Ukai, Y.、Kimura, K.、Tanaka, T.、Yano, J.、Moriyama, N. 等人:“人类前列腺尿道中 α_1-肾上腺素受体亚型的鉴定”。 Arch.Pharmacol.355。412-416 (1997)
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Moriyama,N., et al.: "Immunohistochemical expression of glucose transporter 1 in human penile proliferative lesions." Histochemical J.29. 273-278 (1997)
Moriyama,N. 等人:“人类阴茎增殖性病变中葡萄糖转运蛋白 1 的免疫组织化学表达。”
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Homma,Y., Akaza,H., Okada,K., Yokoyama,M., Moriyama,N., et al.: "Preoperative endocrine therapy for clinical stage A2,B,and C prostate cancer : An interim report on short-term effect." Int.J.Urol.4. 144-151 (1997)
Homma,Y.、Akaza,H.、Okada,K.、Yokoyama,M.、Moriyama,N. 等人:“临床 A2、B 和 C 期前列腺癌的术前内分泌治疗:关于短期的中期报告
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Moriyama,N., et al.: "KMD-3213,a novel α_<1a>-adrenoceptor antagonist,potently inhibits the functional α_1-adrenoceptor in human prostate." Eur.J.Pharmacol.331. 39-42 (1997)
Moriyama,N.等人:“KMD-3213,一种新型α_1a-肾上腺素受体拮抗剂,有效抑制人前列腺中的功能性α_1-肾上腺素受体。”Eur.J.Pharmacol.331(1997)。
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海外基金