A novel protein quality control system and its role in tumorigenesis

一种新型蛋白质质量控制系统及其在肿瘤发生中的作用

基本信息

批准号：
10558619
负责人：
Xiaolu Yang
金额：
$ 44.47万
依托单位：
UNIVERSITY OF PENNSYLVANIA
依托单位国家：
美国
项目类别：
财政年份：
2020
资助国家：
美国
起止时间：
2020-02-01 至 2025-07-31
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10558619
关键词：
Address Amino Acid Motifs Animal Model Animals Antioxidants Binding Caenorhabditis elegans Cell Death Cell model Cells Characteristics Clinical Crowding Development Environment Evolution Excision Goals Growth Human Impairment Knowledge Life Maintenance Malignant Neoplasms Mammalian Cell Mediating Molecular Molecular Conformation Mus Normal Cell Oncogenic Oxidative Stress PML gene Process Production Proliferating Proteasome Inhibition Proteasome Inhibitor Proteins Proteolysis Quality Control Role Signal Transduction Stress Sumoylation Pathway System TRIM Motif TRIM11 gene Testing Ubiquitination Up-Regulation cancer cell cancer initiation cancer therapy carcinogenesis effective therapy macromolecule malignant phenotype member misfolded protein multicatalytic endopeptidase complex neoplastic cell novel protein degradation protein folding protein misfolding proteostasis trait tumor tumor progression tumorigenesis ubiquitin ligase virtual

项目摘要

PROJECT DESCRIPTION The overall goal of this application is to characterize a novel protein quality control (PQC) system in mammalian cells and to elucidate its role in tumorigenesis. Oncogenic transformation is a progressive process during which normal cells acquire a set of traits to overcome various constraints that govern their proliferation. Here we will test the notion that a heightened ability to remove misfolded proteins may be a new characteristic of tumor cells. Protein folding is a challenging process in normal unstressed cells, and even more so in incipient and established neoplastic cells, which frequently encounter high oxidative stresses that damage proteins. However, PQC systems that remove misfolded proteins in mammalian cells and the role of these systems in tumorigenesis are not well understood. Our lab recently found that many mammalian tripartite motif (TRIM) proteins can specifically recognize misfolded proteins and mark them for proteasomal degradation, and that certain TRIM can also directly activate the proteasome. Moreover, we observed that the capacity to remove misfolded proteins is markedly increased in cancer cells due to the up-regulation of TRIMs. This higher degradation power mitigates oxidative stress associated with oncogenic growth and permits oncogenic growth. These findings indicate TRIMs as versatile regulators of protein quality, connect the clearance of misfolded proteins to antioxidant defense, and suggest a previously unrecognized characteristic of tumor cells. Our central hypothesis is that TRIM proteins constitute a major PQC system in mammalian cells that are critical for antioxidant defense and oncogenic transformation. We propose three specific aims. First, TRIM proteins exist in a large number including over 70 in humans. To gain a comprehensive view of the TRIM system, we will systematically investigate the role of all human TRIMs in proteasomal degradation of misfolded proteins and define the molecular basis for their different potency. Second, we will investigate how the accumulation of misfolded proteins causes high oxidative stress, and how TRIMs ameliorate this stress through the clearance of misfolded proteins. Third, we will determine the role of the TRIM system in cancer progression using cell and animal models. Moreover, our results suggest that the removal of misfolded protein is highly sensitive to proteasome inhibition, which may provide an explanation for proteasome-inhibitor-based therapies for cancer. We will test the notion that increasing production of misfolded proteins, combined with proteasome blockage, may be highly effective in killing cancer cells. Collectively, these aims will address critical issues pertaining to protein homeostasis and oncogenic transformation, and will likely provide valuable information for the development of effective therapies.

项目描述该应用的总体目标是表征哺乳动物中的新型蛋白质质量控制 (PQC) 系统细胞并阐明其在肿瘤发生中的作用。致癌转化是一个渐进的过程，在此过程中正常细胞获得一系列特征来克服控制其增殖的各种限制。在这里我们将检验这样一种观点：去除错误折叠蛋白质的能力增强可能是肿瘤细胞的一个新特征。在正常未受应激的细胞中，蛋白质折叠是一个具有挑战性的过程，在初期和已建立的细胞中更是如此。肿瘤细胞经常遇到高氧化应激，从而损害蛋白质。然而，PQC 消除哺乳动物细胞中错误折叠蛋白质的系统以及这些系统在肿瘤发生中的作用不太理解。我们的实验室最近发现许多哺乳动物三联基序（TRIM）蛋白可以特异性地识别错误折叠的蛋白质并将其标记为蛋白酶体降解，并且某些 TRIM 还可以直接激活蛋白酶体。此外，我们观察到去除错误折叠蛋白质的能力显着增强。由于 TRIM 的上调，癌细胞数量增加。这种更高的降解能力可以减轻氧化与致癌生长相关的应激并允许致癌生长。这些发现表明 TRIM 作为蛋白质质量的多功能调节剂，将错误折叠蛋白质的清除与抗氧化防御联系起来，以及表明肿瘤细胞具有以前未被识别的特征。我们的中心假设是 TRIM 蛋白构成哺乳动物细胞中的主要 PQC 系统，对于抗氧化防御和致癌至关重要转变。我们提出三个具体目标。首先，TRIM蛋白大量存在，包括70多种在人类中。为了全面了解 TRIM 系统，我们将系统地研究所有人类 TRIM 在错误折叠蛋白的蛋白酶体降解中的作用，并定义了其不同的分子基础效力。其次，我们将研究错误折叠蛋白质的积累如何导致高氧化应激，以及 TRIM 如何通过清除错误折叠的蛋白质来缓解这种压力。第三，我们将确定使用细胞和动物模型研究 TRIM 系统在癌症进展中的作用。此外，我们的结果表明错误折叠蛋白的去除对蛋白酶体抑制高度敏感，这可能提供了一个解释用于基于蛋白酶体抑制剂的癌症疗法。我们将检验增加产量的观点错误折叠的蛋白质与蛋白酶体阻断相结合，可能非常有效地杀死癌细胞。总的来说，这些目标将解决与蛋白质稳态和致癌相关的关键问题转化，并可能为开发有效疗法提供有价值的信息。

项目成果

期刊论文数量（2）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Autophagy and pluripotency: self-eating your way to eternal youth.

自噬和多能性：自我吞噬通往永恒青春的道路。

DOI：
10.1016/j.tcb.2022.04.001
发表时间：
2022-10
期刊：
Trends in cell biology
影响因子：
19
作者：
Xu, Yi;Yang, Xiaolu
通讯作者：
Yang, Xiaolu

TRIM11 Prevents and Reverses Protein Aggregation and Rescues a Mouse Model of Parkinson's Disease.

TRIM11 预防和逆转蛋白质聚集并拯救帕金森病小鼠模型。

DOI：
10.1016/j.celrep.2020.108418
发表时间：
2020-12-01
期刊：
Cell reports
影响因子：
8.8
作者：
Zhu G;Harischandra DS;Ghaisas S;Zhang P;Prall W;Huang L;Maghames C;Guo L;Luna E;Mack KL;Torrente MP;Luk KC;Shorter J;Yang X
通讯作者：
Yang X