相关实验视频
Updated: Jul 5, 2025

09:33
Methods to Classify Cytoplasmic Foci as Mammalian Stress Granules
Published on: May 12, 2017
14.6K
压力颗粒通过调节线粒体未折叠蛋白质反应来影响双PI3K/mTOR抑制剂反应
Nan Lin1,2, Liankun Sun2, Jiannan Chai3
1First Hospital of Jilin University, Changchun, China.
Cancer cell international
|January 18, 2024
概括
压力颗粒 (SGs) 通过拦截ATF5和调节线粒体反应,促进卵巢癌的耐药性. 准SG可能为抗药性卵巢癌提供新的策略.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 细胞应激反应的应激反应
背景情况:
- 药物耐药性是治疗卵巢癌的一个主要障碍.
- 适应性应激反应,特别是应激颗粒 (SGs),越来越被认为是抗癌药物耐药性的关键机制.
研究的目的:
- 研究压力颗粒 (SGs) 在卵巢癌细胞中介于耐药性的作用.
- 探索SG,信号因子和药物治疗下的器官反应之间的相互作用.
主要方法:
- 使用了A2780和SKOV3卵巢癌细胞系.
- 用双PI3K/mTOR抑制剂PKI-402治疗的细胞.
- 分析了压力颗粒的形成及其与ATF5的相互作用以及线粒体展开蛋白质反应 (UPR).
主要成果:
- 在A2780卵巢癌细胞中,PKI-402诱导了压力颗粒的形成.
- 压力颗粒被发现可以拦截信号因子ATF5.5.
- 压力颗粒的形成与线粒体展开蛋白质反应 (UPR) 的调节有关.
结论:
- 压力颗粒在适应性应激反应中起着重要作用,有助于卵巢癌的耐药性.
- 压力颗粒和信号通路 (如ATF5) 和器官细胞反应 (如UPR) 之间的相互作用对于理解耐药性至关重要.
- 研究SG和膜结合器官的网络为抗瘤药物机制提供了新的见解.
相关概念视频
PI3K/mTOR/AKT Signaling Pathway
3.6K
The mammalian target of rapamycin (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast, mTORC2 consists of a...
3.6K
mTOR Signaling and Cancer Progression
3.8K
The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
The mTOR pathway or the...
3.8K
Regulation of the Unfolded Protein Response
2.4K
Inositol-requiring kinase one or IRE1 is the most conserved eukaryotic unfolded protein response (UPR) receptor. It is a type I transmembrane protein kinase receptor with a distinctive site-specific RNase activity. As the binding mechanics of the misfolded proteins with the N-terminal domain of IRE-1 are unclear, three binding models — direct, indirect, and allosteric -- are proposed for receptor activation. Nevertheless, it is known that once a misfolded protein associates with IRE1, it...
2.4K
The Unfolded Protein Response
4.6K
The ER is the hub of protein synthesis in a cell. It has robust systems to quality control protein folding and also for degradation of terminally misfolded proteins. Under normal conditions, a small proportion of misfolded proteins that cannot be salvaged need to be transported to the cytoplasm by the ER-associated degradation or ERAD pathways. However, if the ERAD cannot handle the misfolded proteins, the cell activates the unfolded protein response or UPR to adjust the protein folding...
4.6K
Interactions Between Signaling Pathways
6.3K
Signaling cascades usually lack linearity. Multiple pathways interact and regulate one another, allowing cells to integrate and respond to diverse environmental stimuli.
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
6.3K
MAPK Signaling Cascades
5.5K
Mitogen-activated protein kinase, or MAPK pathway, activates three sequential kinases to regulate cellular responses such as proliferation, differentiation, survival, and apoptosis. The canonical MAPK pathway starts with a mitogen or growth factor binding to an RTK. The activated RTKs stimulate Ras, which recruits Raf or MAP3 Kinase (MAPKKK), the first kinase of the MAPK signaling cascade. Raf further phosphorylates and activates MEK or MAP2 Kinases (MAPKK), which in turn phosphorylates MAP...
5.5K

