Breast Cancer Diagnosis: Blood-Cell Multigene Signatures

乳腺癌诊断：血细胞多基因特征

• 批准号: 6676260
• 负责人: CATHERINE L CLELLAND
• 金额: $ 16.95万
• 依托单位: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-07-01 至 2005-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6676260
• 关键词: breast neoplasms; clinical research; computer data analysis; diagnosis design /evaluation; diagnosis quality /standard; gene expression; genetic screening; genetic transcription; human subject; leukocytes; mathematics; microarray technology; neoplasm /cancer classification /staging; neoplasm /cancer diagnosis; neoplasm /cancer genetics; neoplastic process; patient oriented research; polymerase chain reaction; women's health

DESCRIPTION (provided by applicant): Current techniques for the screening of breast cancer, as a prerequisite to biopsy for diagnostic evaluation of a potential tumor, include physical breast examination and mammography. These techniques possess a number of limitations, including lack of specificity and accuracy in the diagnosis and, also a lack of cancer stage and prognostic information. This ultimately yields high numbers of false positive diagnoses, and consequently unnecessarily large numbers of surgical biopsies. The rationale behind this proposal is based on two sources of data: 1) Current scientific literature, in which there is growing evidence that individuals with breast cancer and other forms of malignant disease such as prostate cancer, exhibit immune responses that can be detected at the level of altered gene expression in leukocytes circulating in peripheral blood. Quantitation of the mRNA transcripts in leukocytes of a number of individual genes has demonstrated associations between gene expression levels and the presence of a tumor in patients with breast and prostate cancer. 2) Preliminary results from a microarray study investigating gene expression changes in men with prostate cancer. Initial results from this study have been striking; supervised cluster analysis of peripheral leukocyte gene expression data, using transcript level measurements of thousands of genes from eleven prostate cancer patients and seven matched control subjects, resulted in a classification of all the subjects into their correct group. These observations form the basis of the hypothesis and experimental design of this proposed study. Under Specific Aim One, we will collect and process blood from 55 breast cancer patients and 25 healthy control subjects. We will then employ microarray technology to measure simultaneously the expression levels of up to 14,000 genes transcribed in leukocytes derived from the blood of breast cancer patients and control subjects, and employ data analysis algorithms to determine patterns of gene expression specific for each subject group. With this technology we propose to investigate our central hypothesis: that individuals suffering from breast cancer exhibit a conserved pattern of gene expression levels in their peripheral blood leukocytes, which is distinct from the pattern of expression in peripheral blood leukocytes from control subjects. Under Specific Aim Two, we will test the further hypothesis that cancer patients with breast tumors at different histological grades will yield distinct expression signatures that reflect the biological stage and aggressiveness of the tumor, and that can thus be employed to differentiate among tumors at different pathological stages. We believe that the diagnostic technique we propose to develop may ultimately form the basis of a clinical assay that will, with a minimum of patient discomfort, have the capacity to identify women with breast cancer, and also provide important stage-specific information.

描述（由申请方提供）：作为活检以诊断评估潜在肿瘤的先决条件，目前用于筛查乳腺癌的技术包括乳房物理检查和乳房X线摄影。这些技术具有许多局限性，包括缺乏诊断的特异性和准确性，以及缺乏癌症分期和预后信息。这最终产生大量的假阳性诊断，并因此产生不必要的大量手术活检。这一提议背后的基本原理基于两个数据来源：1）当前的科学文献，其中有越来越多的证据表明，患有乳腺癌和其他形式的恶性疾病（如前列腺癌）的个体表现出免疫应答，可以在外周血中循环的白细胞中改变的基因表达水平上检测到。白细胞中许多单个基因的mRNA转录物的定量已经证明了乳腺癌和前列腺癌患者中基因表达水平与肿瘤存在之间的关联。2)来自微阵列研究的初步结果，研究前列腺癌男性的基因表达变化。这项研究的初步结果是惊人的;外周血白细胞基因表达数据的监督聚类分析，使用来自11名前列腺癌患者和7名匹配的对照受试者的数千个基因的转录水平测量，导致所有受试者被分类到正确的组中。这些观察结果构成了这项拟议研究的假设和实验设计的基础。根据具体目标一，我们将收集和处理55名乳腺癌患者和25名健康对照受试者的血液。然后，我们将采用微阵列技术同时测量来自乳腺癌患者和对照受试者血液的白细胞中转录的多达14，000个基因的表达水平，并采用数据分析算法来确定每个受试者组的基因表达模式。通过这项技术，我们建议调查我们的中心假设：患有乳腺癌的个体在其外周血白细胞中表现出保守的基因表达水平模式，这与对照受试者外周血白细胞中的表达模式不同。在具体目标二下，我们将检验进一步的假设，即具有不同组织学分级的乳腺肿瘤的癌症患者将产生不同的表达特征，其反映肿瘤的生物学阶段和侵袭性，并且因此可以用于区分不同病理阶段的肿瘤。我们相信，我们建议开发的诊断技术可能最终形成临床检测的基础，该检测将以最小的患者不适为基础，有能力识别患有乳腺癌的女性，并提供重要的阶段特异性信息。