Functions of BNIP3 in Mammary Tumorigenesis

BNIP3 在乳腺肿瘤发生中的功能

基本信息

批准号：
7663515
负责人：
KAY F MACLEOD
金额：
$ 31.52万
依托单位：
UNIVERSITY OF CHICAGO
依托单位国家：
美国
项目类别：
财政年份：
2009
资助国家：
美国
起止时间：
2009-02-01 至 2013-12-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7663515
关键词：
Affect Animals Apoptotic Arts Autophagocytosis Autophagosome Biological Assay Biological Markers Brain Carcinoma Cell Death Cells Cultured Cells Data Family Goals Human Hypoxia Imaging Techniques In Vitro Incidence Infiltration Inflammation Inflammatory Response Intervention Life Liver Lung Malignant Neoplasms Mammary Neoplasms Mammary Tumorigenesis Metastatic Lesion Metastatic Neoplasm to the Lung Mitochondria Molecular Monitor Mus Necrosis Neoplasm Metastasis Nuclear Nuclear Export Play Point Mutation Primary Neoplasm Reactive Oxygen Species Reporting Research Proposals Role Signal Transduction Site-Directed Mutagenesis Small Interfering RNA Staging Structure Testing Time Tumor Cell Line Tumor Volume Woman Work Xenograft procedure base bone bone xenograft cancer diagnosis clinically significant experience imaging modality in vivo insight knockout gene macrophage malignant breast neoplasm member mitochondrial autophagy molecular marker mouse model neoplastic cell novel outcome forecast prevent public health relevance response tumor tumor progression uptake

项目摘要

DESCRIPTION (provided by applicant): Breast cancer metastasis to the lungs, bones, liver and brain is the fatal stage in the most common form of cancer diagnosed annually in women in the US. Tumor hypoxia and necrosis are tightly correlated with metastasis and poor prognosis in breast cancer, although the molecular basis of this correlation is not well defined. BNIP3 is a hypoxia- inducible regulator of cell death and loss of BNIP3 activity increased the metastatic potential of breast tumor cell lines in mouse xenografts. Mechanistic studies from our lab have indicated a critical role for BNIP3 in promoting autophagy and limiting necrosis in mammary tumor cells in culture. The current work will extend our molecular insight into the functions of BNIP3 by examining the molecular mechanism underlying the role of BNIP3 in targeting mitochondria for autophagy and how this contributes to the adaptive response of breast tumor cells to hypoxia (Aim 1). Making use of primary tumor arrays, we will examine the statistical significance of BNIP3 levels and altered sub-cellular localization for predicting progression of human breast cancer (Aim 2). Using structure-function analyses, we examine molecular mechanisms that may explain BNIP3 inactivation during breast cancer progression (Aim 2). The proposed work will also use state-of-the-art imaging techniques to monitor BNip3 expression during mammary tumor progression and metastasis in mouse models of breast cancer and to monitor the effect of BNip3 gene knockout on the incidence and latency of breast tumor metastasis to the lungs in cancer-prone mice (Aim 3). This work has clinical significance by identifying BNIP3 as a putative marker of breast cancer progression and defining a novel role for BNIP3 as a metastasis suppressor. PUBLIC HEALTH RELEVANCE: Metastasis is the last and most deadly step in the progression of human cancers and in the case of breast cancer the spread of tumor cells to the lungs, bones, liver and brain is a poor prognosis for survival. The significance of the current work lies in defining inactivation of BNIP3 as a marker of tumor progression, characterizing its molecular function and mechanism of inactivation in primary human breast cancer, and in determining whether it functions as a metastasis suppressor. Using data from primary human breast cancers and from mouse models to determine whether BNIP3 plays a role in preventing breast cancer metastasis, our work aims to determine whether BNIP3 might be useful as a molecular marker of breast cancer progression and if intervention to prevent BNIP3 inactivation is likely to reduce the incidence of breast cancer metastasis.

描述（由申请人提供）：乳腺癌转移至肺部、骨骼、肝脏和大脑是美国女性每年诊断出的最常见癌症的致命阶段。肿瘤缺氧和坏死与乳腺癌的转移和不良预后密切相关，尽管这种相关性的分子基础尚不清楚。 BNIP3 是一种缺氧诱导的细胞死亡调节剂，BNIP3 活性的丧失增加了小鼠异种移植物中乳腺肿瘤细胞系的转移潜力。我们实验室的机制研究表明 BNIP3 在促进培养的乳腺肿瘤细胞自噬和限制坏死方面发挥着关键作用。目前的工作将通过检查 BNIP3 在靶向线粒体自噬中的作用的分子机制，以及这如何促进乳腺肿瘤细胞对缺氧的适应性反应，扩展我们对 BNIP3 功能的分子洞察（目标 1）。利用原发性肿瘤芯片，我们将检查 BNIP3 水平和改变的亚细胞定位的统计显着性，以预测人类乳腺癌的进展（目标 2）。通过结构功能分析，我们研究了可能解释乳腺癌进展过程中 BNIP3 失活的分子机制（目标 2）。拟议的工作还将使用最先进的成像技术来监测乳腺癌小鼠模型中乳腺肿瘤进展和转移过程中 BNip3 的表达，并监测 BNip3 基因敲除对乳腺肿瘤转移的发生率和潜伏期的影响。易患癌症小鼠的肺部（目标 3）。这项工作具有临床意义，将 BNIP3 确定为乳腺癌进展的推定标志物，并确定了 BNIP3 作为转移抑制因子的新作用。公共健康相关性：转移是人类癌症进展的最后一步也是最致命的一步，对于乳腺癌而言，肿瘤细胞扩散到肺、骨骼、肝脏和大脑是生存预后不良的情况。目前工作的意义在于将 BNIP3 失活定义为肿瘤进展的标志物，表征其在原发性人类乳腺癌中的分子功能和失活机制，并确定其是否具有转移抑制因子的功能。使用来自原发性人类乳腺癌和小鼠模型的数据来确定 BNIP3 是否在预防乳腺癌转移中发挥作用，我们的工作旨在确定 BNIP3 是否可用作乳腺癌进展的分子标记，以及预防 BNIP3 失活的干预措施是否有效可能会降低乳腺癌转移的发生率。