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mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

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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...
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PI3K/mTOR/AKT Signaling Pathway01:22

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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...
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Interactions Between Signaling Pathways01:19

Interactions Between Signaling Pathways

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Signaling cascades usually lack linearity. Multiple pathways interact and regulate one another, allowing cells to integrate and respond to diverse environmental stimuli.
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Regulation of Food Intake01:30

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Short-term regulation of food intake primarily involves neural signals from the gastrointestinal (GI) tract, blood nutrient levels, and GI tract hormones. Communication between the gut and brain via vagal nerve fibers plays a significant role in evaluating the contents of the gut. Clinical studies have shown that protein ingestion produces a more prolonged response in these nerve fibers compared to an equivalent amount of glucose. Additionally, the activation of stretch receptors caused by GI...
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Regulation of the Unfolded Protein Response01:31

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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...
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NF-κB-dependent Signaling Pathway02:26

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The transcription factor NF-κB was discovered in 1986 in the lab of Nobel laureate Professor David Baltimore, for its interaction with the immunoglobulin light chain enhancer in B-cells. After more than three decades of study, it is now evident that NF-κB regulates the expression of over 100 genes. Most of these genes play an essential role in the innate and adaptive immune responses as well as the inflammatory responses of animals.
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Updated: May 30, 2025

Author Spotlight: Exploring Salidroside's Molecular Mechanisms in Breast Cancer Treatment
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硫甲急性激活了多个饥饿反应途径.

Kendra S Plafker1, Constantin Georgescu2, Nathan Pezant3

  • 1Aging and Metabolism Research Program, Oklahoma City, OK, United States.

Frontiers in nutrition
|January 27, 2025
PubMed
概括

硫黄 (SFN) 是一种来自十字花蔬菜的化合物,通过激活细胞饥饿反应来模仿禁食. 这种禁食模仿效应可以解释SFN的治疗益处和潜在的毒性.

关键词:
塞斯特林 2 塞斯特林这是一个Txnipp.自自是自的过程.在mTOROR中使用mTOR.饥饿 饥饿 饥饿 饥饿 饥饿硫甲是一种硫甲.

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科学领域:

  • 生物化学 生物化学
  • 细胞生物学 细胞生物学
  • 营养科学 营养科学

背景情况:

  • 硫酸盐 (SFN) 是一种来自十字花植物的异酸盐,具有已知的抗癌,抗微生物和抗氧化特性.
  • 在动物疾病模型中,SFN已经显示出效果,类似于饮食限制,促使对其禁食模仿潜力的调查.

研究的目的:

  • 调查硫 (SFN) 是否引起与禁食或卡路里限制相一致的细胞反应.
  • 探索SFN对人类视网膜色素上皮细胞中营养感知通路的影响.

主要方法:

  • 用SFN治疗人类视网膜色素上皮细胞的不朽化.
  • 分析线粒体质量,抗氧化压力,mTORC1/2活性,胰岛素信号,自,溶酶体生物发生,葡萄糖吸收和乳酸分泌.
  • 测量硫素相互作用蛋白 (TXNIP) 和酸盐脱酶酸化.
  • 分析糖溶性和三碳酸 (TCA) 循环中间体.
  • RNA测序 (RNA-seq) 用于识别转录的变化.

主要成果:

  • SFN增加了线粒体质量和氧化应激抵抗力.
  • 通过抑制胰岛素信号传递和上调自和溶酶体生物发生,SFN抑制了mTORC1/2的活动.
  • SFN急性降低了葡萄糖摄取和乳酸分泌,与抑制的TXNIP相关的反弹.
  • SFN改变了代谢中间体,并促进了pyruvate进入TCA循环,这表明了饥饿反应.
  • RNA-seq证实了对饥饿反应的转录程序的激活.

结论:

  • 通过影响关键营养感应通路,SFN表现出禁食模仿性质.
  • 这些禁食模仿效应可能有助于硫福拉的治疗疗效和潜在毒性.
  • SFN对代谢途径的影响表明,SFN在细胞适应营养缺乏的过程中发挥了作用.