Re-activation of maspin tumor suppressor gene by designed transcription factors

设计的转录因子重新激活maspin抑癌基因

• 批准号: 8026864
• 负责人: Lee M Graves
• 金额: $ 26.91万
• 依托单位: UNIV OF NORTH CAROLINA CHAPEL HILL
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-05-01 至 2013-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8026864
• 关键词: Affect; Affinity; Animal Model; Apoptosis; Apoptotic; Base Pairing; Binding; Bioinformatics; Biological Assay; Bioluminescence; Breast; Breast Cancer Cell; Breast Cancer Model; Cancer Patient; Cancer cell line; Cell Line; Cells; Chromatin; Chromatin Structure; Complementary DNA; Critical Pathways; DNA; DNA Microarray Chip; Deoxycytidine; Dependovirus; Disease Progression; Down-Regulation; Engineering; Epigenetic Process; Epithelial; Extracellular Matrix; Extracellular Matrix Proteins; Fatty acid glycerol esters; Foundations; Gene Silencing; Genes; Genetic Transcription; Histone Acetylation; Histone Deacetylase Inhibitor; Histones; Hormone Receptor; Hydroxamic Acids; Image; Implant; In Vitro; Lead; Limes; Link; Luciferases; MCF7 cell; Malignant Neoplasms; Mammary Neoplasms; Mammary gland; Maps; Measures; Mediating; Metastatic Lesion; Methylation; Methyltransferase; Modeling; Molecular; Monitor; Mutate; Mutation; Neoplasm Metastasis; Nude Mice; Organ; Peptide Hydrolases; Pharmaceutical Preparations; Phase II Clinical Trials; Primary Neoplasm; Procedures; Process; Prostate; Prostatic Neoplasms; Protease Inhibitor; Proteins; Regulation; Relaxation; Reporter; Research Personnel; Retroviral Vector; Role; SERPINB5 gene; Serine Proteinase Inhibitors; Signal Pathway; Signal Transduction; Site; Specificity; Therapeutic; Time; Tissues; Transactivation; Transcription Coactivator; Transcription Factor AP-1; Transcriptional Regulation; Trichostatin A; Tumor Cell Invasion; Tumor Cell Line; Tumor Suppression; Tumor Suppressor Genes; Tumor Suppressor Proteins; Western Blotting; Work; Xenograft Model; Xenograft procedure; Zinc Fingers; activating transcription factor; angiogenesis; annexin A5; base; biological adaptation to stress; cancer cell; cancer therapy; cancer type; cell motility; chromatin immunoprecipitation; chromatin remodeling; design; design and construction; genome wide association study; genome-wide; histone methyltransferase; inhibitor/antagonist; malignant breast neoplasm; maspin; matrigel; methyl group; migration; mouse model; neoplastic; neoplastic cell; novel; novel strategies; novel therapeutics; overexpression; programs; promoter; small molecule; therapeutic target; time use; transcription factor; tumor; tumor growth; tumor progression

DESCRIPTION (provided by applicant): During tumor progression, cancer cells undergo dynamic transformations, including tumor growth, angiogenesis, and metastatic dissemination. There is a crucial need in cancer therapeutics to develop novel approaches that target critical, ideally multiple steps, during tumor progression. In this proposal, we have designed artificial transcription factors (ATFs) made of zinc finger (ZF) domains as novel therapeutic strategy to inhibit multiple processes during tumor progression. We have targeted the mammary serine protease inhibitor (maspin) gene (SERPINB5), Maspin is an important therapeutic target since its overexpression is associated with tumor suppression, decreased angiogenesis, motility and metastasis in breast and prostate tumor models. Metastatic cells have developed several mechanisms to down-regulate maspin. Maspin is rarely mutated in aggressive tumors. Instead, silencing of maspin involves both, transcriptional regulation and aberrant promoter methylation. Our objective is to construct ATFs able to specifically re-activate maspin in metastatic breast cell lines, overcoming epigenetic silencing. Our hypothesis is that ATFs up-regulating maspin, by themselves or in combination with drugs that increase chromatin accessibility (methyltransferase and histone deacetylase inhibitors), will be able to re-activate maspin functions in tumor cells, reduce tumor growth and metastatic spread in nude mice. First, we have engineered highly specific ATFs made of 6ZF domains targeting 18-base pairs (bp) sites in the maspin promoter. The ZFs are linked to a potent transcriptional activator domain and expressed in tumor cells using retroviral vectors. We will investigate if the ATFs are able to specifically reactivate maspin in several breast cancer cells comprising a methylated and silenced maspin promoter. We will study if the ATFs synergize with methyltransferase and histone deacetylase inhibitors, to up-regulate maspin. We will assess if these ATFs are able to down-regulate cell invasion and to induce apoptosis in metastatic cell lines. Finally, the ATFs will be expressed using Adeno- Associated Viruses (AAVs) and we will study their capability to down-regulate tumor growth and metastasis in an orthotopic xenograft model of breast cancer in nude mice. Metastatic lesions will be monitored in real time using Bioluminescence Imaging (BLI). This work should lead to the characterization of novel anti-cancer regulators, able to reprogram the aberrant epigenetic silencing of tumor suppressors

描述（由申请人提供）：在肿瘤进展过程中，癌细胞经历动态转化，包括肿瘤生长、血管生成和转移传播。在癌症治疗中，迫切需要开发针对肿瘤进展过程中关键的、理想的多个步骤的新方法。在本研究中，我们设计了由锌指结构域（ZF）构成的人工转录因子（ATFs）作为抑制肿瘤进展过程中多个过程的新治疗策略。我们针对乳腺丝氨酸蛋白酶抑制剂（maspin）基因（SERPINB5）， maspin是一个重要的治疗靶点，因为它的过表达与乳腺和前列腺肿瘤模型中的肿瘤抑制、血管生成减少、运动和转移有关。转移细胞已经发展出几种下调maspin的机制。Maspin在侵袭性肿瘤中很少发生突变。相反，maspin的沉默涉及转录调控和异常启动子甲基化。我们的目标是构建能够在转移性乳腺细胞系中特异性重新激活maspin的ATFs，克服表观遗传沉默。我们的假设是，ATFs上调maspin，单独或与增加染色质可及性的药物（甲基转移酶和组蛋白去乙酰化酶抑制剂）联合，将能够重新激活肿瘤细胞中的maspin功能，减少裸鼠肿瘤生长和转移性扩散。首先，我们设计了高度特异性的atf，由6ZF结构域组成，靶向maspin启动子中的18个碱基对（bp）位点。zf与一个有效的转录激活子结构域相连，并通过逆转录病毒载体在肿瘤细胞中表达。我们将研究atf是否能够在几种乳腺癌细胞中特异性地重新激活含有甲基化和沉默的maspin启动子的maspin。我们将研究ATFs是否与甲基转移酶和组蛋白去乙酰化酶抑制剂协同作用，以上调maspin。我们将评估这些ATFs是否能够下调细胞侵袭并诱导转移细胞系的细胞凋亡。最后，我们将使用腺相关病毒（aav）表达ATFs，并在裸鼠原位乳腺癌异种移植模型中研究其下调肿瘤生长和转移的能力。转移性病变将使用生物发光成像（BLI）进行实时监测。这项工作将导致表征新的抗癌调节因子，能够重新编程肿瘤抑制因子的异常表观遗传沉默

项目成果

A highly efficient synthetic vector: nonhydrodynamic delivery of DNA to hepatocyte nuclei in vivo.

• DOI: 10.1021/nn4012384
• 发表时间: 2013-06-25
• 期刊: ACS NANO
• 影响因子: 17.1
• 作者: Hu, Yunxia;Haynes, Matthew T.;Wang, Yuhua;Liu, Feng;Huang, Leaf
• 通讯作者: Huang, Leaf

Novel role of Engrailed 1 as a prosurvival transcription factor in basal-like breast cancer and engineering of interference peptides block its oncogenic function.

• DOI: 10.1038/onc.2013.422
• 发表时间: 2014-09-25
• 期刊: Oncogene
• 影响因子: 8
• 作者: Beltran AS;Graves LM;Blancafort P
• 通讯作者: Blancafort P

Suppression of breast tumor growth and metastasis by an engineered transcription factor.

• DOI: 10.1371/journal.pone.0024595
• 发表时间: 2011
• 期刊: PloS one
• 影响因子: 3.7
• 作者: Beltran AS;Russo A;Lara H;Fan C;Lizardi PM;Blancafort P
• 通讯作者: Blancafort P

Expression of the Pluripotency Transcription Factor OCT4 in the Normal and Aberrant Mammary Gland.

• DOI: 10.3389/fonc.2013.00079
• 发表时间: 2013
• 期刊: Frontiers in oncology
• 影响因子: 4.7
• 作者: Hassiotou F;Hepworth AR;Beltran AS;Mathews MM;Stuebe AM;Hartmann PE;Filgueira L;Blancafort P
• 通讯作者: Blancafort P

Breastmilk is a novel source of stem cells with multilineage differentiation potential.

• DOI: 10.1002/stem.1188
• 发表时间: 2012-10
• 期刊: STEM CELLS
• 影响因子: 5.2
• 作者: Hassiotou, Foteini;Beltran, Adriana;Chetwynd, Ellen;Stuebe, Alison M.;Twigger, Alecia-Jane;Metzger, Philipp;Trengove, Naomi;Lai, Ching Tat;Filgueira, Luis;Blancafort, Pilar;Hartmann, Peter E.
• 通讯作者: Hartmann, Peter E.