Induction of cancer cell death by selective DNA misincorporation

通过选择性 DNA 错误掺入诱导癌细胞死亡

• 批准号: 8845341
• 负责人: Derek James Taylor
• 金额: $ 18.63万
• 依托单位: CASE WESTERN RESERVE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-09-15 至 2018-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8845341
• 关键词: Adult; Aging-Related Process; Apoptosis; Binding; Cancer Biology; Cancer cell line; Cell Death; Cell division; Cells; DNA; DNA Damage; DNA Sequence; Enzymes; Event; Human; Human Chromosomes; Malignant Neoplasms; Measures; Nucleotides; Role; Telomerase; Telomere Capping; Telomere Shortening; Telomere-Binding Proteins; Therapeutic; Tissues; Tumor Suppressor Proteins; Xenograft procedure; cancer cell; cell killing; design; innovation; mouse model; normal aging; novel; nucleotide analog; telomere

DESCRIPTION (provided by applicant): Telomeres cap and protect the ends of all human chromosomes. In healthy adult tissue, telomeres shorten with each round of cell division as part of the normal aging process. This mechanism limits human cells to a finite number of cell divisions before induction of programmed cell death and therefore serves as a tumor suppressor. In cancer cells, however, an enzyme called telomerase is upregulated to nullify the limited number of cell divisions. As such, cancer cells are capable of infinite division, which allows proliferation of ~90% of all malignant tumors. Due to this unique and critical role in cancer biology, telomerase provides a novel target for innovative therapeutics. The purpose of the present proposal is to explore a novel mechanism toward using telomerase as an anti-cancer target. In our approach, we will design non-native nucleotide analogs to be preferentially and selectively incorporated by telomerase into telomere DNA. Once incorporated, the non-native nucleotides should abrogate binding of essential telomere-end binding proteins such as the Protection of Telomeres 1 (POT1), which is highly specific for telomere DNA sequence. Abrogation of POT1 binding induces cell death through a cascade of DNA damage events. The cell-killing potential of these non-native nucleotide compounds will be validated by measuring their potency and selectivity against telomerase-positive cancer cell lines as well as xenograft mouse models. We predict that our strategy will provide a selective mechanism to potentially treat a wide range of human cancers.

描述（由申请人提供）：端粒覆盖并保护所有人类染色体的末端。在健康的成人组织中，端粒随着每一轮细胞分裂而缩短，这是正常衰老过程的一部分。这种机制将人类细胞限制在有限数量的细胞分裂，然后诱导程序性细胞死亡，因此可以作为肿瘤抑制因子。然而，在癌细胞中，一种叫做端粒酶的酶被上调，以抵消有限的细胞分裂次数。因此，癌细胞能够无限分裂，这允许所有恶性肿瘤的~90%增殖。由于端粒酶在癌症生物学中的独特和关键作用，端粒酶为创新疗法提供了新的靶点。本研究的目的是探索端粒酶作为抗癌靶点的新机制。在我们的方法中，我们将设计非天然的核苷酸类似物优先和选择性地纳入端粒DNA的端粒酶。一旦掺入，非天然核苷酸应消除必需的端粒末端结合蛋白如端粒保护1（POT 1）的结合，其对端粒DNA序列具有高度特异性。POT 1结合的取消通过一系列DNA损伤事件诱导细胞死亡。这些非天然核苷酸化合物的细胞杀伤潜力将通过测量其对端粒酶阳性癌细胞系以及异种移植小鼠模型的效力和选择性来验证。我们预测，我们的策略将提供一种选择性机制，有可能治疗多种人类癌症。

项目成果

Advances in structure determination by cryo-EM to unravel membrane-spanning pore formation.

冷冻电镜结构测定的进展揭示了跨膜孔的形成。

• DOI: 10.1002/pro.3454
• 发表时间: 2018
• 期刊: Protein science : a publication of the Protein Society
• 作者: Scott,Harry;Huang,Wei;Bann,JamesG;Taylor,DerekJ
• 通讯作者: Taylor,DerekJ

Multiple facets of TPP1 in telomere maintenance.

• DOI: 10.1016/j.bbapap.2014.04.014
• 发表时间: 2014-09
• 期刊: BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS
• 影响因子: 3.2
• 作者: Rajavel, Malligarjunan;Mullins, Michael R.;Taylor, Derek J.
• 通讯作者: Taylor, Derek J.

Dynamic peptides of human TPP1 fulfill diverse functions in telomere maintenance.

• DOI: 10.1093/nar/gkw846
• 发表时间: 2016-12-01
• 期刊: Nucleic acids research
• 影响因子: 14.9
• 作者: Rajavel M;Orban T;Xu M;Hernandez-Sanchez W;de la Fuente M;Palczewski K;Taylor DJ
• 通讯作者: Taylor DJ