Molecular Species Responsible for Tumor Supressive Effect of MnSOD

负责 MnSOD 肿瘤抑制作用的分子种类

基本信息

批准号：
8014965
负责人：
FREDERICK E DOMANN
金额：
$ 24.21万
依托单位：
UNIVERSITY OF IOWA
依托单位国家：
美国
项目类别：
财政年份：
2007
资助国家：
美国
起止时间：
2007-04-01 至 2013-01-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8014965
关键词：
Abbreviations Affect Amitrole Antioxidants Breast Buthionine Sulfoximine Carmustine Cell Proliferation Cells Chemicals Complementary DNA Copper Data Deoxyglucose Ensure Enzymes Equilibrium Excision Genes Glioma Glucose Glucosephosphate Dehydrogenase Glutamate-Cysteine Ligase Glutathione Glutathione Disulfide Glutathione Reductase Growth Human Hydrogen Peroxide Infection Inhibition of Cancer Cell Growth Knowledge Location MCF7 cell MDA MB 231 Malignant - descriptor Manganese Manganese Superoxide Dismutase Measures Mitochondria Molecular Nitric Oxide Nitric Oxide Synthase Nitrogen Nitrosourea Compounds Non-Malignant Normal Cell Organelles Oxidation-Reduction Oxygen Pathway interactions Peroxidases Phosphogluconate Dehydrogenase Phospholipids Play Proteins Reactive Oxygen Species Reduced Glutathione Research Research Personnel Role Signal Transduction Pathway Small Interfering RNA Specificity Superoxide Dismutase Superoxides Transfection Tumor Suppression Tumor Suppressor Proteins U118 Work Zinc anticancer treatment base cancer cell cancer therapy cancer type catalase cell type clinically relevant copper zinc superoxide dismutase dehydroepiandrosterone experience glioma cell line glucose oxidase glutathione peroxidase glutathione synthase inhibitor/antagonist malignant breast neoplasm malignant phenotype peroxiredoxin peroxisome phospholipid-hydroperoxide glutathione peroxidase programs protein expression research study tumor

项目摘要

The mitochondria! antioxidant enzyme manganese-containing superoxide dismutase (MnSOD) has been shown to be a tumor suppressor in a wide variety of different cancer cell types. In this application, we propose to examine the mechanism of tumor suppression by MnSOD. We will examine which reactive oxygen or nitrogen species is involved. We propose that there are only three logical possibilities: superoxide radical, hydrogen peroxide, or nitric oxide radical. We will transfect the cDNA for proteins that affect these molecules into MnSOD over-expressing human breast cancer and glioma cell lines and determine the effect on the malignant phenotype. The other proteins that will be over-expressed include two forms of glutathione peroxidase, catalase, and nitric oxide synthase. Moreover, the effect of inhibiting the activity of these proteins will be determined. Inhibition of glutathione peroxidase, catalase, and nitric oxide synthase will be accomplished by chemical inhibitors as well as antisense oligodeoxynucleotides and siRNAs. We will also transfect glucose oxidase into cancer cells and examine the effect on the malignant phenotype. Glucose oxidase produces hydrogen peroxide when glucose is present as substrate and thus this experiment will examine further if hydrogen peroxide is the effector molecule. If we can determine the molecular effector of the growth inhibitory effect of MnSOD over-expression, then we can use that knowledge to develop new anticancer treatments based on MnSOD over-expression and inhibition of the effector removal pathway. For example, we already have data showing hydrogen peroxide is involved in the growth suppressive effect of MnSOD over-expression and so we plan to study the antitumor effect of MnSOD over-expression combined with inhibitors of hydrogen peroxide removal. In this way, we hope to be able to develop exciting new cancer therapies.

线粒体！含有锰锰的超氧化物歧化酶（MNSOD）的抗氧化剂酶已经被证明是多种不同癌细胞类型的肿瘤抑制剂。在此应用程序中，我们建议检查MNSOD抑制肿瘤的机制。我们将检查哪个反应性涉及氧或氮。我们建议只有三种逻辑可能性：超氧化物自由基，过氧化氢或一氧化氮自由基。我们将转染影响这些影响这些的蛋白质分子到MNSOD过表达的人类乳腺癌和神经胶质瘤细胞系，并确定效果在恶性表型上。其他将过表达的蛋白质包括两种形式的谷胱甘肽过氧化物酶，过氧化氢酶和一氧化氮合酶。而且，抑制这些活性的效果将确定蛋白质。抑制谷胱甘肽过氧化物酶，过氧化氢酶和一氧化氮合酶将是通过化学抑制剂以及反义寡脱氧核苷酸和siRNA完成。我们也会将葡萄糖氧化酶转染到癌细胞中，并检查对恶性表型的影响。葡萄糖当葡萄糖作为底物存在时，氧化酶会产生过氧化氢，因此该实验将进一步检查过氧化氢是否是效应分子。如果我们可以确定 MNSOD过表达的增长抑制作用，然后我们可以利用这些知识来发展新的基于MNSOD过表达和抑制效应子去除途径的抗癌处理。为了例如，我们已经有数据表明过氧化氢与 MNSOD过表达，因此我们计划研究MNSOD过表达的抗肿瘤效应与过氧化氢去除的抑制剂。这样，我们希望能够发展出令人兴奋的新癌症疗法。

项目成果

期刊论文数量（6）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Mitochondrial calcium uniporter activity is dispensable for MDA-MB-231 breast carcinoma cell survival.

DOI：
10.1371/journal.pone.0096866
发表时间：
2014
期刊：
PloS one
影响因子：
3.7
作者：
Hall DD;Wu Y;Domann FE;Spitz DR;Anderson ME
通讯作者：
Anderson ME

Prolyl-4-hydroxylase 3 (PHD3) expression is downregulated during epithelial-to-mesenchymal transition.

DOI：
10.1371/journal.pone.0083021
发表时间：
2013
期刊：
PloS one
影响因子：
3.7
作者：
Place TL;Nauseef JT;Peterson MK;Henry MD;Mezhir JJ;Domann FE
通讯作者：
Domann FE

Disruption of thioredoxin metabolism enhances the toxicity of transforming growth factor β-activated kinase 1 (TAK1) inhibition in KRAS-mutated colon cancer cells.

DOI：
10.1016/j.redox.2015.06.004
发表时间：
2015-08
期刊：
REDOX BIOLOGY
影响因子：
11.4
作者：
Hrabe, Jennifer E.;O'Leary, Brianne R.;Fath, Melissa A.;Rodman, Samuel N.;Button, Anna M.;Domann, Frederick E.;Spitz, Douglas R.;Mezhir, James J.
通讯作者：
Mezhir, James J.

Integrin α3β1 can function to promote spontaneous metastasis and lung colonization of invasive breast carcinoma.

DOI：
10.1158/1541-7786.mcr-13-0184
发表时间：
2014-01
期刊：
Molecular cancer research : MCR
影响因子：
0
作者：
Zhou B;Gibson-Corley KN;Herndon ME;Sun Y;Gustafson-Wagner E;Teoh-Fitzgerald M;Domann FE;Henry MD;Stipp CS
通讯作者：
Stipp CS