EXPRESSION BASED MARKERS FOR BREAST CANCER DETECTION
用于乳腺癌检测的基于表达的标记物
基本信息
- 批准号:6377758
- 负责人:
- 金额:$ 41.24万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1999
- 资助国家:美国
- 起止时间:1999-09-30 至 2004-08-31
- 项目状态:已结题
- 来源:
- 关键词:antibody formation biomarker breast neoplasm /cancer diagnosis cancer information system cell line circulating neoplastic cell clinical research cooperative study diagnosis design /evaluation female flow cytometry gene expression genetic library human subject immunomagnetic separation in situ hybridization mammary epithelium molecular oncology northern blottings polymerase chain reaction telomerase tissue resource /registry women's health
项目摘要
This proposal will attempt to identify expression-based markers for breast cancer and develop assays using these markers to detect circulating breast cancer cells. Our application has been developed as a collaborative effort between the Duke Breast Cancer Program and Abbott Diagnostic Breast Cancer Venture Group and will utilize the considerable strengths of each institution. The basic approach for marker identification takes advantage of ongoing (and separately funded) efforts using powerful new genomics tools. At Duke, SAGE (serial analysis of gene expression) libraries of breast cancer and normal breast epithelium are being constructed as part of CGAP. Also at Duke, a series of 20 primary breast cancers will be analyzed using high-density Affymetrix expression chips (30,000 genes/ESTs will be sampled). Finally, at Abbott Diagnostics, markers have already been identified by using the Incyte Corporation expression libraries. These three sources of expression data will be compared electronically and the most promising markers that are expressed at high levels in a tissue or cancer specific manner will be identified. After the in silico analysis, the lead markers will be put through a validation algorithm that will include northern blotting, multiple tissue RNA dot blots, RT-PCR, and in situ cytohybridization. A panel of breast cell lines and a series of 50 primary breast cancers will be used to determine how commonly expressed these markers are in the target tissue. After these initial validation steps, a series of reconstitution experiments will be performed by spiking normal whole blood with known numbers of breast cancer cells, derived from cell lines and malignant effusions. Epithelial cells will be purified using magnetic bead/antibody technology and the resulting purified samples will be analyzed by flow cytometry, histology, and quantitative RT-PCR. Towards increasing sensitivity, a separate and parallel screen will focus on markers that are highly overexpressed in a subset of breast cancers. PCR multiplexing approaches will be explored in this context and will also include using telomerase gene (TERT) expression as a cancer specific marker in conjunction with other lead markers. Antibodies to the most promising candidates will be developed, particularly for gene products that may be secreted or presented on the cell surface. Finally, a collection of whole blood and serum samples will be obtained from women newly diagnosed with breast cancer at Duke. This bank will constitute a primary validation set for markers and approaches that have proven to be the most robust.
该提案将尝试识别基于表达的乳腺癌标记物,并开发使用这些标记物检测循环乳腺癌细胞的检测方法。 我们的应用程序是杜克乳腺癌计划和雅培诊断乳腺癌风险投资集团合作开发的,并将利用每个机构的巨大优势。标记物识别的基本方法利用了使用强大的新基因组学工具正在进行的(并且单独资助的)努力。 杜克大学正在构建乳腺癌和正常乳腺上皮的 SAGE(基因表达系列分析)文库,作为 CGAP 的一部分。 同样在杜克大学,将使用高密度 Affymetrix 表达芯片对一系列 20 个原发性乳腺癌进行分析(将采样 30,000 个基因/EST)。 最后,在 Abbott Diagnostics,标记已经通过使用 Incyte Corporation 表达库进行了鉴定。 这三种表达数据来源将以电子方式进行比较,并且将鉴定出以组织或癌症特异性方式高水平表达的最有希望的标记物。 计算机分析后,先导标记将通过验证算法,其中包括 Northern 印迹、多组织 RNA 点印迹、RT-PCR 和原位细胞杂交。 一组乳腺细胞系和一系列 50 种原发性乳腺癌将用于确定这些标记物在目标组织中表达的普遍程度。在这些初步验证步骤之后,将通过在正常全血中掺入已知数量的来自细胞系和恶性渗出物的乳腺癌细胞来进行一系列重建实验。 将使用磁珠/抗体技术纯化上皮细胞,并通过流式细胞术、组织学和定量 RT-PCR 分析所得纯化样品。 为了提高敏感性,一个单独的并行筛选将重点关注在乳腺癌子集中高度过度表达的标记物。 PCR 多重方法将在此背景下进行探索,还将包括使用端粒酶基因 (TERT) 表达作为癌症特异性标记物与其他先导标记物结合使用。 将开发针对最有希望的候选者的抗体,特别是针对可能分泌或呈现在细胞表面上的基因产物。 最后,将从杜克大学新诊断出患有乳腺癌的女性中采集全血和血清样本。 该库将为已被证明最可靠的标记和方法构成主要验证集。
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)
数据更新时间:{{ journalArticles.updateTime }}
{{
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 }}
Jeffrey R. Marks其他文献
Loss of expression of the p16 tumor suppressor gene is more frequent in advanced ovarian cancers lacking p53 mutations.
在缺乏 p53 突变的晚期卵巢癌中,p16 肿瘤抑制基因的表达缺失更为常见。
- DOI:
- 发表时间:
2001 - 期刊:
- 影响因子:4.7
- 作者:
L. Havrilesky;A. A. Alvarez;R. Whitaker;Jeffrey R. Marks;A. Berchuck - 通讯作者:
A. Berchuck
A clinicogenomic model to predict lymph node metastasis in breast cancer
- DOI:
10.1016/j.jamcollsurg.2008.06.092 - 发表时间:
2008-09-01 - 期刊:
- 影响因子:
- 作者:
Melissa E. Danko;Brian R. Untch;Christopher L. Tebbit;Jun Zhai;Holly K. Dressman;Rex C. Bentley;Jay Baker;Jeffrey R. Marks;Joseph R. Nevins;John A. Olson - 通讯作者:
John A. Olson
Relative promoter activity in human mammary epithelial cells assayed by transient expression
通过瞬时表达测定人乳腺上皮细胞中的相对启动子活性
- DOI:
10.1007/bf02631061 - 发表时间:
1992 - 期刊:
- 影响因子:0
- 作者:
G. Huper;Jeffrey R. Marks;Jon R. Wiener;J. Iglehart - 通讯作者:
J. Iglehart
Spatial localization of collagen hydroxylated proline site variation as an ancestral trait in the breast cancer microenvironment
胶原蛋白羟基脯氨酸位点变异的空间定位作为乳腺癌微环境中的一个祖先特征
- DOI:
10.1016/j.matbio.2025.01.006 - 发表时间:
2025-04-01 - 期刊:
- 影响因子:4.800
- 作者:
Harrison Taylor;Laura Spruill;Heather Jensen-Smith;Denys Rujchanarong;Taylor Hulahan;Ashlyn Ivey;Alex Siougiannis;Jennifer R. Bethard;Lauren E. Ball;George E. Sandusky;M.A. Hollingsworth;Jeremy L. Barth;Anand S. Mehta;Richard R. Drake;Jeffrey R. Marks;Harikrishna Nakshatri;Marvella Ford;Peggi M. Angel - 通讯作者:
Peggi M. Angel
Can BI-RADS features on mammography be used as a surrogate for expensive genomic testing in breast cancer patients?
乳腺 X 线摄影的 BI-RADS 特征能否替代乳腺癌患者进行昂贵的基因组检测?
- DOI:
10.1117/12.2255866 - 发表时间:
2017 - 期刊:
- 影响因子:0
- 作者:
Michael R. Harowicz;Jeffrey R. Marks;P. Marcom;M. Mazurowski - 通讯作者:
M. Mazurowski
Jeffrey R. Marks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('Jeffrey R. Marks', 18)}}的其他基金
EXPRESSION BASED MARKERS FOR BREAST CANCER DETECTION
用于乳腺癌检测的基于表达的标记物
- 批准号:
6074223 - 财政年份:1999
- 资助金额:
$ 41.24万 - 项目类别:
EXPRESSION BASED MARKERS FOR BREAST CANCER DETECTION
用于乳腺癌检测的基于表达的标记物
- 批准号:
6175287 - 财政年份:1999
- 资助金额:
$ 41.24万 - 项目类别:
Atlantic Breast and Gynecologic Clinical Validation Center
大西洋乳腺和妇科临床验证中心
- 批准号:
8505386 - 财政年份:1999
- 资助金额:
$ 41.24万 - 项目类别:
EXPRESSION BASED MARKERS FOR BREAST CANCER DETECTION
用于乳腺癌检测的基于表达的标记物
- 批准号:
6522548 - 财政年份:1999
- 资助金额:
$ 41.24万 - 项目类别:
Expression Based Markers for Breast Cancer Detection
用于乳腺癌检测的基于表达的标记
- 批准号:
6952363 - 财政年份:1999
- 资助金额:
$ 41.24万 - 项目类别:
Expression Based Markers for Breast Cancer Detection
用于乳腺癌检测的基于表达的标记
- 批准号:
7281761 - 财政年份:1999
- 资助金额:
$ 41.24万 - 项目类别:
Atlantic Breast and Gynecologic Clinical Validation Center
大西洋乳腺和妇科临床验证中心
- 批准号:
8706680 - 财政年份:1999
- 资助金额:
$ 41.24万 - 项目类别:
相似国自然基金
基于DNA甲基化交互网络的癌症hallmark挖掘及其在癌症转移biomarker筛选中的应用
- 批准号:61602201
- 批准年份:2016
- 资助金额:20.0 万元
- 项目类别:青年科学基金项目
血清miRNAs成为一种新的biomarker在PD诊断中的价值和LRRK2基因调控的机制研究
- 批准号:81170309
- 批准年份:2011
- 资助金额:50.0 万元
- 项目类别:面上项目
非小细胞肺癌Biomarker的Imaging MS研究新方法
- 批准号:30672394
- 批准年份:2006
- 资助金额:30.0 万元
- 项目类别:面上项目
相似海外基金
酸化ストレス応答アポトーシス誘導蛋白のUCに対する新規Biomarker探索と治療への展開
寻找治疗 UC 的氧化应激反应性凋亡诱导蛋白的新生物标志物并开发治疗方法
- 批准号:
24K11919 - 财政年份:2024
- 资助金额:
$ 41.24万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
肝内胆管癌新規Biomarkerの同定及び癌周囲間質を標的とした新規治療開発
鉴定肝内胆管癌的新型生物标志物并开发针对癌周基质的新疗法
- 批准号:
24K19350 - 财政年份:2024
- 资助金额:
$ 41.24万 - 项目类别:
Grant-in-Aid for Early-Career Scientists
収縮能が保たれた心不全の機械学習分類とmicroRNAなどのbiomarkerの探索
机器学习对具有保留收缩性的心力衰竭进行分类并搜索 microRNA 等生物标志物
- 批准号:
24K19007 - 财政年份:2024
- 资助金额:
$ 41.24万 - 项目类别:
Grant-in-Aid for Early-Career Scientists
Development of a predictive biomarker for Parkinson's disease
帕金森病预测生物标志物的开发
- 批准号:
MR/Y019415/1 - 财政年份:2024
- 资助金额:
$ 41.24万 - 项目类别:
Research Grant
Sleep and circadian dysfunction in ageing and neurodegeneration: a life course and biomarker study of the British 1946 birth cohort.
衰老和神经退行性疾病中的睡眠和昼夜节律功能障碍:对英国 1946 年出生队列的生命历程和生物标志物研究。
- 批准号:
MR/Y009452/1 - 财政年份:2024
- 资助金额:
$ 41.24万 - 项目类别:
Fellowship
Biomarker-Based Platform for Early Diagnosis of Chronic Liver Disease to Enable Personalized Therapy (LIVERAIM)
基于生物标志物的慢性肝病早期诊断平台,以实现个性化治疗(LIVERAIM)
- 批准号:
10087822 - 财政年份:2024
- 资助金额:
$ 41.24万 - 项目类别:
EU-Funded
Enhanced stratification of COPD patients via integration of a digitally enabled biomarker Point-of-Care test within a Remote Patient Monitoring tool
通过在远程患者监测工具中集成数字化生物标志物即时检测,增强 COPD 患者的分层
- 批准号:
10098600 - 财政年份:2024
- 资助金额:
$ 41.24万 - 项目类别:
Collaborative R&D
QuBIE: Quantitative Biomarker Identification for Non-Endoscopic Prediction and Monitoring of Treatment Response in Eosinophilic Oesophagitis
QuBIE:用于非内镜预测和监测嗜酸性食管炎治疗反应的定量生物标志物鉴定
- 批准号:
10083253 - 财政年份:2024
- 资助金额:
$ 41.24万 - 项目类别:
Collaborative R&D
膵癌腫瘍内線維化に着目した術前化学療法効果予測に関する画像biomarkerの確立
建立预测胰腺癌瘤内纤维化术前化疗效果的影像生物标志物
- 批准号:
24K18824 - 财政年份:2024
- 资助金额:
$ 41.24万 - 项目类别:
Grant-in-Aid for Early-Career Scientists
I-Corps: Developing A Blood-Based Biomarker for the Detection and Monitoring of Amyotrophic Lateral Sclerosis
I-Corps:开发一种基于血液的生物标志物,用于检测和监测肌萎缩侧索硬化症
- 批准号:
2317745 - 财政年份:2023
- 资助金额:
$ 41.24万 - 项目类别:
Standard Grant














{{item.name}}会员




