Angiogenesis in female genital tract cancers and its inhibition
Angiogenesis in female genital tract cancers and its inhibition
批准号:
11671606
负责人:
FUJIMOTO Jiro
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:
1999
资助国家:
日本
项目状态:
已结题
起止时间:
1999 至 2001
中文摘要
以血小板衍化内皮细胞生长因子(PD-ECGF)标记的胸苷磷酸化酶(TP)在宫颈癌中的表达与微血管密度和患者预后相关。尤其是从原发肿瘤到转移淋巴结的PD-ECGF水平升高被认为是判断患者预后的更敏感的指标。此外,无论组织学类型如何,血清PD-ECGF均可作为宫颈癌进展的一种新的肿瘤标志物。宫颈癌中血管生成转录因子Ets-1与PD-ECGF和IL-8相关由于PD-EGGF和ETS-1可通过血管生成促进生长和继发扩散,因此由5-氟尿嘧啶、PD-ECGF底物和ETS-1抑制剂组成的掩蔽化合物可能对宫颈癌有效,尤其是在转移的淋巴结上。卵巢癌组织中血管内皮生长因子亚型…的表达More-65和Ets-1与患者预后相关,但与组织学类型和临床分期无关,尤其是在腹膜转移灶中。由于VEGF和ETS-1可通过血管生成促进卵巢癌的生长和继发扩散,因此,VEGF受体酪氨酸激酶抑制剂、抗VEGF抗体和ETS-1抑制剂可能对卵巢癌,特别是腹膜转移性病变有效。碱性成纤维细胞生长因子在子宫内膜癌中的表达与临床分期有关。PD-ECGF和VEGF的表达受性激素的部分调控,可能与子宫内膜癌的早期发展有关。IL-8在子宫肌层侵袭中被诱导并达到峰值,可能作为血管生成开关发挥作用。Ets-1在高分化子宫内膜癌中的表达与血管内皮生长因子的表达呈正相关,在低分化子宫内膜癌中的表达与bFGF的表达呈正相关。因此,必须针对与临床分期和分化程度相关的靶血管生成因子,抑制子宫内膜癌的特异性血管生成,从而达到高效治疗子宫内膜癌的目的。较少
英文摘要
In uterine cervical cancers, the expression of thymidine phosphorylase ( TP ) identified with platelefrderived endothelial cell growth factor ( PD-ECGF ) correlated with microvessel density and patient prognosis. Especially, the increased level of PD-ECGF from the primary tumor to metastatic lymph nodes was recognized as a more sensitive indicator for patient prognosis. Furthermore, serum PD-ECGF can be used a novel tumor marker for advancement of uterine cervical cancers regardless of histopathological types. The transcription factor ets-1 for angiogenesis linked to PD-ECGF and interleukin ( IL )-8 in uterine cervical cancers. As PD-EGGF and ets-1 can be considered to promote growth and secondary spreading via angiogenesis, masked compounds of 5-fluorouracil, substrates of PD-ECGF, and ets-1 inhibitors might be effective on uterine cervical cancers, especially on the metastatic lymph nodes. In ovarian cancers, the expression of vascular endothelial growth factor ( VEGF ) isoform VEGFi … More 65 and ets-1 correlated with patient prognosis, but not with histopathological types and clinical stages, especially in metastatic peritoneal lesions. As VEGF and ets-1 can be considered to promote growth and secondary spreading via angiogenesis, VEGF receptor tyrosine kinase inhibitors, anti-VEGF antibodies and ets-1 inhibitors might be effective on ovarian cancers, especially on metastatic peritoneal lesions. In uterine endometrial cancers, the expression of basic fibroblast growth factor ( bFGF ) correlated with clinical stages. The expression of PD-ECGF and VEGF was partially regulated by sex steroids, and they might grow the early stage of uterine endometrial cancers. IL-8 was induced and reached to the peak level in myometrial invasion, and might work as an angiogenic switch. The expression of ets-1 in well-differentiated uterine endometrial cancers correlated with that of VEGF, and the expression of ets-1 in poorly differentiated uterine endometrial cancers correlated with that of bFGF. Therefore, the target angiogenic factors associated with clinical stages and differentiated grades must be attacked to suppress the specific angiogenesis, which might lead to highly effective treatment with uterine endometrial cancers. Less
期刊论文(46)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
Fujimoto J., et al.: "The value of platelet-derived endothelial cell growth factor (PD-ECGF) as a novel predictor of advancement of uterine cervical cancers"Cancer Res.. 60. 3662-3665 (2000)
Fujimoto J.等人:“血小板源性内皮细胞生长因子(PD-ECGF)作为子宫颈癌进展的新预测因子的价值”Cancer Res.. 60. 3662-3665 (2000)
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Fuiimoto,J., Sakaguchi,H., Hirose,R., Ichigo,S., Tamaya,T.: "Expression of vascular endothelial growth factor ( VEGF ) and its mRNA in uterine cervical cancers"Br J Cancer. 80. 827-833 (1999)
Fuiimoto,J.、Sakaguchi,H.、Hirose,R.、Ichigo,S.、Tamaya,T.:“血管内皮生长因子 ( VEGF ) 及其 mRNA 在子宫颈癌中的表达”Br J Cancer。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Fuiimoto,J., Sakaguchi,H., Hirose,R., Ichigo,S., Tamaya,T.: "Progestin supress estrogen-induced expression of vascular endothelial growth factor ( VEGF ) subtypes in uterine endometrial cancer cells"Cancer Lett. 141. 63-71 (1999)
Fuiimoto,J.、Sakaguchi,H.、Hirose,R.、Ichigo,S.、Tamaya,T.:“孕激素抑制雌激素诱导的子宫内膜癌细胞中血管内皮生长因子 (VEGF) 亚型的表达”Cancer Lett。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Fujimoto J, et al.: "Theexpression of vascular endothelial growth factor and its mRNA in uterine crervical cancers."Br.J.Cancer. 80. 827-833 (1999)
Fujimoto J 等人:“血管内皮生长因子及其 mRNA 在子宫沟癌中的表达。”Br.J.Cancer。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Fujimoto J., et al.: "Clinical implication of exprssion of vascular endothelial growth factor in metastatic lesions of ovarian cancers"Br. J. Cancer. 85. 313-316 (2001)
Fujimoto J. 等人:“血管内皮生长因子表达在卵巢癌转移性病变中的临床意义”Br。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
共 41 条
Proposal and verification the hypothesis "coagulation,IFNγ andPAI-1 control liver fibrosis and carcinogenesis mechanism"
-
批准号:23659660
-
项目类别:Grant-in-Aid for Challenging Exploratory Research
-
资助金额:$2.33万
-
财政年份:2011
-
负责人:FUJIMOTO Jiro
-
依托单位:
Analysis of molecular mechanism and the regulation of adhesion
-
批准号:22390250
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$12.15万
-
财政年份:2010
-
负责人:FUJIMOTO Jiro
-
依托单位:
Establishment of experimental surgical adhesion model and analysis of immunological mechanism underlying organ adhesion
-
批准号:19390342
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$11.9万
-
财政年份:2007
-
负责人:FUJIMOTO Jiro
-
依托单位:
Analysis of the role of angiogenesis and non-parenchymal cells during hepatic regeneration.
-
批准号:17390375
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$9.54万
-
财政年份:2005
-
负责人:FUJIMOTO Jiro
-
依托单位:
Angiogenesis and tumor dormancy therapy in gynecological cancer
-
批准号:14370528
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$7.62万
-
财政年份:2002
-
负责人:FUJIMOTO Jiro
-
依托单位:
Basic research and clinical approach of molecular therapy for liver cirrhosis and HCC
-
批准号:14370395
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$7.62万
-
财政年份:2002
-
负责人:FUJIMOTO Jiro
-
依托单位:
Functional analysis of LATS protein kinases, products of novel tumor-suppressor genes
-
批准号:12670130
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$1.6万
-
财政年份:2000
-
负责人:FUJIMOTO Jiro
-
依托单位:
GENE THERAPY OF LIVER CIRRHOSIS ; BASIC RESEARCH AND A PROSPECT FOR CLINICAL TRIAL
-
批准号:11470266
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$8.9万
-
财政年份:1999
-
负责人:FUJIMOTO Jiro
-
依托单位:
Functional analysis of FAK tyrosine kinase in intracellular signaling pathways
-
批准号:09680668
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$0.9万
-
财政年份:1997
-
负责人:FUJIMOTO Jiro
-
依托单位:
Study of endocrinological contribution for invasion and metastasis in gynecological cancers
-
批准号:08671881
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$1.47万
-
财政年份:1996
-
负责人:FUJIMOTO Jiro
-
依托单位:
In vivo gene transduction in hepatoma using monoclonal antibody or specific promotor.
-
批准号:07457282
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$4.8万
-
财政年份:1995
-
负责人:FUJIMOTO Jiro
-
依托单位:
Study of mechanisms of development and growth in hormone (especially estrogen) dependent uterine tumor and its related diseases.
-
批准号:06671638
-
项目类别:Grant-in-Aid for General Scientific Research (C)
-
资助金额:$1.09万
-
财政年份:1994
-
负责人:FUJIMOTO Jiro
-
依托单位:
Difference of sensitivity to the chemoprevention (cisplatin vs.cv-3611 or SOD) between young and gerontic mice
-
批准号:06671269
-
项目类别:Grant-in-Aid for General Scientific Research (C)
-
资助金额:$0.26万
-
财政年份:1994
-
负责人:FUJIMOTO Jiro
-
依托单位:
Suppression ofdevelopment of spontaneous and cisplatin-induced malignant
-
批准号:04670779
-
项目类别:Grant-in-Aid for Scientific Research (C).
-
资助金额:$0.45万
-
财政年份:1992
-
负责人:FUJIMOTO Jiro
-
依托单位:
Effects of recombinant human superoxide dismutase and 2-0-octadecylascorbic acid on survival of tumor bearing mice and on side effects of bleomycin and adriamycin
-
批准号:63570633
-
项目类别:Grant-in-Aid for General Scientific Research (C)
-
资助金额:$0.45万
-
财政年份:1988
-
负责人:FUJIMOTO Jiro
-
依托单位:
Difference in histologic effects on the liver with regard to the route of administration of fluorinated pyrimidines in gastric cancer patients
-
批准号:60570624
-
项目类别:Grant-in-Aid for General Scientific Research (C)
-
资助金额:$0.77万
-
财政年份:1985
-
负责人:FUJIMOTO Jiro
-
依托单位:
国内基金
海外基金
登录
查看更多内容
TGF-β/lnc-APUE/ZEB1通路促进肝癌转移的机制及生物学意义
-
批准号:32100616
-
项目类别:青年科学基金项目(C类)
-
资助金额:30.0万元
-
批准年份:2021
-
负责人:李颂扬
-
依托单位:
乳腺癌细胞外泌体miRNA诱导组蛋白修饰表观调控巨噬细胞M2极化的机制探索
-
批准号:31960152
-
项目类别:地区科学基金项目
-
资助金额:39.0万元
-
批准年份:2019
-
负责人:罗达亚
-
依托单位:
内质网蛋白Ei24调控胰腺癌细胞迁移、侵袭的分子机制研究
-
批准号:31970704
-
项目类别:面上项目
-
资助金额:50.0万元
-
批准年份:2019
-
负责人:袁琳
-
依托单位:
泛素连接酶TRIM65通过RhoGAP调控Rho活性促进结直肠癌侵袭转移的分子机制
-
批准号:31970703
-
项目类别:面上项目
-
资助金额:50.0万元
-
批准年份:2019
-
负责人:陈代词
-
依托单位:
HDAC11去ε-氨基长链脂肪酰化机制及功能的研究
-
批准号:31970749
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2019
-
负责人:孙蕾
-
依托单位:
FSTL1诱导结直肠癌相关成纤维细胞活化的分子机制研究
-
批准号:31900569
-
项目类别:青年科学基金项目
-
资助金额:24.0万元
-
批准年份:2019
-
负责人:谷川莎
-
依托单位:
E3泛素连接酶RNF8在肺癌转移中的作用及机制研究
-
批准号:31900537
-
项目类别:青年科学基金项目
-
资助金额:24.0万元
-
批准年份:2019
-
负责人:匡静宇
-
依托单位:
靶向纳米颗粒调控HIF-1α通路抑制缺氧三阴性乳腺癌耐药和转移的研究
-
批准号:31900567
-
项目类别:青年科学基金项目
-
资助金额:24.0万元
-
批准年份:2019
-
负责人:田浩
-
依托单位:
癌蛋白TBC1D3与β-肌动蛋白“对话”促进乳腺癌细胞迁移的分子机制
-
批准号:31801171
-
项目类别:青年科学基金项目
-
资助金额:21.0万元
-
批准年份:2018
-
负责人:王北
-
依托单位:
ARHGEF39通过与STRAP相互作用激活TGF-β/Smad信号通路而促进肝癌侵袭转移的机制研究
-
批准号:81802917
-
项目类别:青年科学基金项目
-
资助金额:21.0万元
-
批准年份:2018
-
负责人:王海啸
-
依托单位: