Molecular mechanism of chemoprevention against prostate cancer by phytosterol
Molecular mechanism of chemoprevention against prostate cancer by phytosterol
批准号:
14571510
负责人:
UEMURA Hiroji
金额:
$2.24万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2002
资助国家:
日本
项目状态:
已结题
起止时间:
2002 至 2003
中文摘要
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英文摘要
We investigated how phytosterol such as gensitein play a role in inhibiting the cell growth of prostate cancer. Since 2002 we used androgen dependent cell line, LNCaP, in our experiments. In particular, our experiments focused on telomerase activity associated with cancer cell proliferation. The results indicated that genistein could suppress the transcription of hTERT gene which is one of catalytic subunits of telomerase. Similar results were obtained in experiments using androgen independent PC3 prostate cancer cell. These data revealed that genistein inhibited telomerase activity regardless of androgen dependency.Next, we investigated the expression of nonsteroidal anti-inflammatory drug activated gene 1 (NAG-1) that is activated by nonsteroidal anti-inflammatory drug (NSAID). RT-PCR analysis showed that NAG-1 gene expressed in prostate cancer tissue higher than in normal prostate tissue, and its expression level was associated with the pathological differentiation. When LNCaP cells were stimulated with genistein, it suppressed the expression of NAG-1 in time-and dose-dependent manner.In conclusion, gensitein affected not only telomerase activity but also some genes such as NAG-1 related with prostate cancer. Further investigation of molecular mechanism of which gensitein plays an important role in prostate cancer may lead to the development of new strategy for treatment or chemoprevention of prostate cancer.
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H.Uemura, H Ishiguro, et al.: "Angiotensin II Receptor Blocker Shows Antiproliferative Activity in Prostate Cancer Cells : A Possibility of Tyrosine Kinase Inhibitor of Growth Factor"Molecular Cancer Therapeutics. 2:11. 1139-1147 (2003)
H.Uemura、H Ishiguro 等人:“血管紧张素 II 受体阻滞剂在前列腺癌细胞中显示出抗增殖活性:生长因子酪氨酸激酶抑制剂的可能性”分子癌症治疗。
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Y.Miyoshi, H.Ishiguro, H.Uemura: "Expression of AR associated proteins (ARA55) and androgen receptor in prostate cancer"The Prostate. 56:4. 280-286 (2003)
Y.Miyoshi、H.Ishiguro、H.Uemura:“前列腺癌中 AR 相关蛋白 (ARA55) 和雄激素受体的表达”前列腺。
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K.Mikata, H.Uemura, H.Ohuchi, S.Ohta, Y.Nagashima, Y.Kubota: "Inhibition of growth of human prostate cancer xenograft by transfection of p53 gene : Study of gene transfer by electroporation."Mol Cancer Thera. I. 247-252 (2002)
K.Mikata、H.Uemura、H.Ohuchi、S.Ohta、Y.Nagashima、Y.Kubota:“通过转染 p53 基因抑制人类前列腺癌异种移植物的生长:通过电穿孔进行基因转移的研究。”Mol Cancer Thera
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上村博司: "2003年卒後・生涯教育テキスト(第8巻2号)"化学療法と緩和治療について、第4章「泌尿器科腫瘍」再燃(chemical relapseを含む)前立腺癌の治療:日本泌尿器科学会. 158 (2003)
Hiroshi Uemura:《2003年研究生和继续教育教科书(第8卷第2期)》化疗和姑息治疗,第4章“泌尿肿瘤”前列腺癌的治疗(包括化学复发):日本泌尿外科会议158(2003)。
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H.Ishiguro, H.Uemura, et al.: "55 kDa nuclear matrix (nmt55) mRNA is expressed in human prostate cancer and is associated with androgen receptor."Int.J.Cancer.. 105. 26-32 (2003)
H.Ishiguro、H.Uemura 等人:“55 kDa 核基质 (nmt55) mRNA 在人前列腺癌中表达,并与雄激素受体相关。”Int.J.Cancer.. 105. 26-32 (2003)
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共 25 条
Analysis of the regulation of androgen receptor by renin-angiotensin system in prostate cancer
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项目类别:Grant-in-Aid for Scientific Research (C)
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Analysis of the effect by angiotensin II-induced oxidative stress in the development of prostate cancer
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Analysis of bioactive function of angiotensin II in prostate cancer
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财政年份:2005
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负责人:UEMURA Hiroji
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依托单位:
Functional Analysis of Steroid hormone orphan receptor in hormone refractory prostate cancer
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批准号:11671568
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.37万
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财政年份:1999
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负责人:UEMURA Hiroji
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依托单位:
ANALYSIS OF TR3 RECEPTOR IN APOPTOSIS OF PROSTATE CANCER AND APPLICATION FOR DIAGNOSIS OF PROSTATE CANCER RECCURENCE
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项目类别:Grant-in-Aid for Scientific Research (C)
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负责人:UEMURA Hiroji
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依托单位:
海外基金