Ordermade treatment using analysis of EGFR gene abnormality in non-small cell lung cancer
非小细胞肺癌EGFR基因异常分析的有序治疗
基本信息
- 批准号:17390385
- 负责人:
- 金额:$ 9.28万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (B)
- 财政年份:2005
- 资助国家:日本
- 起止时间:2005 至 2006
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
1. Using probes for the 13 different mutations including 11 that have already been reported, we have genotyped the EGFR mutation status in 400 non small cell lung cancer patients operated between 2000-2006 at Nagoya CityUniversity Hospital using the TaqMan PCR assay.We have evaluated the relationships among the EGFR mutation, clinical-pathologic factors, gefitinib sensitivity, and overall survival.We show in our previous paper that the TaqMan PCR assay is sensitive enough to detect the mutation in samples contaminated with 9 fold excess of wild type samples.Therefore, we have analyzed small samples obtained from CT guided biopsy or trans-bronchial biopsy.2. Some studies reported that downstream signaling molecules, EGFR gene amplification, and the expression of the other ErbB receptors were the other predictors of gefitinib sensitivity. Therefore, we have analyzed the other biomarkers, as the EGFR copy number, the ErbB2 copy number and PIK3CA gene mutation and have evaluated the relationship between their biomarkers and clinical-pathologic factors.3. We have reported these studies at the annual meetings and have published them as an article.4. In the future, we hope that EGFR mutation status using TaqMan PCR assay contributes to made-to-order treatment
1. Using probes for the 13 different mutations including 11 that have already been reported, we have genotyped the EGFR mutation status in 400 non small cell lung cancer patients operated between 2000-2006 at Nagoya CityUniversity Hospital using the TaqMan PCR assay.We have evaluated the relationships among the EGFR mutation, clinical-pathologic factors, gefitinib sensitivity, and overall survival.We show in our previous paper that the TaqMan PCR分析足够敏感,可以检测到被9倍过量的野生型样品污染的样品中的突变。因此,我们分析了从CT引导的活检或跨支气管检查的小样本。2。一些研究报告说,下游信号分子,EGFR基因扩增和其他ERBB受体的表达是吉非替尼灵敏度的其他预测指标。因此,我们已经分析了其他生物标志物,即EGFR拷贝数,ERBB2拷贝数和PIK3CA基因突变,并评估了其生物标志物与临床病理因素之间的关系。3。我们已经在年度会议上报告了这些研究,并将其出版为第4条。将来,我们希望使用TAQMAN PCR测定的EGFR突变状态有助于订购的治疗
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
A Correlation Between EGFR Gene Mutation status and Brochioloalveolar Carcinoma Features in Japanese Patients with Adenocarcinoma
日本腺癌患者 EGFR 基因突变状态与细支气管肺泡癌特征的相关性
- DOI:
- 发表时间:2006
- 期刊:
- 影响因子:0
- 作者:峯田寿裕;田渕和雄;Hidefumi Sasaki;Hiroshi Haneda
- 通讯作者:Hiroshi Haneda
EGFR mutation status and prognosis for gefitinib treatment in Japanese lung cancer
- DOI:10.1016/j.lungcan.2005.09.004
- 发表时间:2006-01-01
- 期刊:
- 影响因子:5.3
- 作者:Sasaki, H;Endo, K;Fujii, Y
- 通讯作者:Fujii, Y
L858R EGFR mutation status correlated with clinico-pathological features of Japanese lung cancer
- DOI:10.1016/j.lungcan.2006.06.003
- 发表时间:2006-10-01
- 期刊:
- 影响因子:5.3
- 作者:Sasaki, Hidefumi;Endo, Katsuhiko;Fujii, Yoshitaka
- 通讯作者:Fujii, Yoshitaka
Epidermal growth factor receptor gene mutation defines distinct subsets among small adenocarcinomas of the lung
- DOI:10.1016/j.lungcan.2005.12.005
- 发表时间:2006-04-01
- 期刊:
- 影响因子:5.3
- 作者:Haneda, H;Sasaki, H;Fujii, Y
- 通讯作者:Fujii, Y
EGFRvIII mutation in lung cancer correlates with increased EGFR copy number.
- DOI:10.3892/or.17.2.319
- 发表时间:2007-02
- 期刊:
- 影响因子:4.2
- 作者:H. Sasaki;O. Kawano;K. Endo;H. Yukiue;M. Yano;Y. Fujii
- 通讯作者:H. Sasaki;O. Kawano;K. Endo;H. Yukiue;M. Yano;Y. Fujii
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
FUJII Yoshitaka其他文献
FUJII Yoshitaka的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('FUJII Yoshitaka', 18)}}的其他基金
Investigation for tyrosine kinase mutations using novel methods
使用新方法研究酪氨酸激酶突变
- 批准号:
23659674 - 财政年份:2011
- 资助金额:
$ 9.28万 - 项目类别:
Grant-in-Aid for Challenging Exploratory Research
Tyrosine kinase gene mutation and chemotherapy sensitivity in lung cancers.
肺癌中酪氨酸激酶基因突变和化疗敏感性。
- 批准号:
21390394 - 财政年份:2009
- 资助金额:
$ 9.28万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Molecular Target Therapy associated with EGFR mutation Analysis in Non-Small Cell Lung Cancer
非小细胞肺癌EGFR突变相关的分子靶向治疗分析
- 批准号:
19390367 - 财政年份:2007
- 资助金额:
$ 9.28万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Antitumor effect utilizing antiangiogenic activity by ribozyme
利用核酶的抗血管生成活性的抗肿瘤作用
- 批准号:
14370416 - 财政年份:2002
- 资助金额:
$ 9.28万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Angiostatin and endostatin gene therapy on murine lung metastases model utilizing cationic vector-mediated intravenous gene delivery
利用阳离子载体介导的静脉内基因递送对小鼠肺转移模型进行血管抑制素和内皮抑制素基因治疗
- 批准号:
11470276 - 财政年份:1999
- 资助金额:
$ 9.28万 - 项目类别:
Grant-in-Aid for Scientific Research (B).
相似国自然基金
基因ytnP克隆表达及其对鲍曼不动杆菌的群体淬灭作用及机制研究
- 批准号:82360003
- 批准年份:2023
- 资助金额:32 万元
- 项目类别:地区科学基金项目
抑癌基因FRMD3缺失诱导小鼠自发三阴乳腺癌的作用和机制研究
- 批准号:82372632
- 批准年份:2023
- 资助金额:46 万元
- 项目类别:面上项目
胃肠道微生物宏基因组的氨基酸消旋酶挖掘及分析
- 批准号:32360034
- 批准年份:2023
- 资助金额:32 万元
- 项目类别:地区科学基金项目
基于群体基因组学解析蒙古高原特有属沙芥属物种形成及适应性演化
- 批准号:32360751
- 批准年份:2023
- 资助金额:32 万元
- 项目类别:地区科学基金项目
FLG基因缺陷促进高毒力ST7型金葡菌在AD患者皮肤定植机制研究
- 批准号:82373458
- 批准年份:2023
- 资助金额:48 万元
- 项目类别:面上项目
相似海外基金
I-Corps: Translation Potential of Rapid In-situ Forming Gel for Local Gene Delivery
I-Corps:快速原位形成凝胶用于局部基因传递的转化潜力
- 批准号:
2410778 - 财政年份:2024
- 资助金额:
$ 9.28万 - 项目类别:
Standard Grant
Conference: 2024 Post-Transcriptional Gene Regulation Gordon Research Conference and Seminar: The Versatility of RNA in the Living World
会议:2024年转录后基因调控戈登研究会议及研讨会:RNA在生活世界中的多功能性
- 批准号:
2422760 - 财政年份:2024
- 资助金额:
$ 9.28万 - 项目类别:
Standard Grant
先天性心疾患原因遺伝子変異に基づくGPCR活性化機構と病態発症機序の解明
基于导致先天性心脏病的基因突变阐明GPCR激活机制和疾病发病机制
- 批准号:
24K11186 - 财政年份:2024
- 资助金额:
$ 9.28万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
気道上皮基底幹細胞の制御とその破綻におけるミトコンドリア内膜因子OPA1の役割の解明
阐明线粒体内膜因子OPA1在气道上皮基底干细胞及其分解调节中的作用
- 批准号:
24K10040 - 财政年份:2024
- 资助金额:
$ 9.28万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
IL-3誘発性の好塩基球前駆細胞増殖における転写因子GATA2の分子機能解明
转录因子GATA2在IL-3诱导的嗜碱性粒细胞祖细胞增殖中的分子功能
- 批准号:
24K10063 - 财政年份:2024
- 资助金额:
$ 9.28万 - 项目类别:
Grant-in-Aid for Scientific Research (C)