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相关概念视频

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The Hedgehog gene (Hh) was first discovered due to its control of the growth of disorganized, hair-like bristles phenotype in Drosophila, much like hedgehog spines. Hh plays a crucial role in the development of organs and the maintenance of homeostasis in both invertebrates and vertebrates. However, while Drosophila has only one Hh protein, mammals have multiple functional Hedgehog proteins - Sonic (Shh), Desert (Dhh), and Indian Hedgehog (Ihh). All of these homologous proteins have adapted to...
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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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Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits.  Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl...
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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.
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Drugs target macromolecules to modify ongoing cellular processes. Primary drug targets include receptors, ion channels, transporters, and enzymes.
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Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as  SH2...
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相关实验视频

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Monitoring Hippo Signaling Pathway Activity Using a Luciferase-based Large Tumor Suppressor LATS Biosensor
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针对TEAD的小分子诱导一个辅因子开关来调节Hippo路径.

Alissa D Guarnaccia1,2, Thijs J Hagenbeek2, Wendy Lee3

  • 1Department of Proteomic and Genomic Technologies, Genentech, South San Francisco, CA 94080.

Proceedings of the National Academy of Sciences of the United States of America
|July 3, 2025
PubMed
概括

新的TEAD抑制剂作为"分子",促进压制性VGLL4-TEAD相互作用. 这种方法通过超越YAP-TEAD复合体来抵消瘤性Hippo通路活性,提供了一种新的癌症治疗策略.

关键词:
河马河马是什么意思 海马河马是什么意思我们的 TEAD TEAD 团队.VGLL4 VGLL4 在线视频癌症治疗疗法 癌症治疗分子粘合剂是分子粘合剂.

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科学领域:

  • 在瘤学瘤学.
  • 分子生物学分子生物学
  • 癌症信号传递 癌症信号传递

背景情况:

  • TEAD蛋白质是Hippo通路信号传导和癌症的关键.
  • 目前的药物向的是TEAD-YAP/TAZ相互作用.
  • 研究了TEAD抑制的一个替代机制.

研究的目的:

  • 调查硫胺化合物对TEAD抑制的一种新机制.
  • 为了确定调节TEAD辅因子相互作用的化合物.
  • 探索VGLL4在TEAD介导的转录调节中的作用.

主要方法:

  • 对 TEAD 向化合物的查.
  • 生物化学分析检测TEAD-辅因子相互作用.
  • 基于细胞的增殖试验.
  • 基因表达分析.
  • 在小鼠模型中的体内研究.

主要成果:

  • 选择的硫胺化合物增强了TEAD与抑制剂VGLL4.4的相互作用.
  • 这种VGLL4-TEAD复合体形成通过取代YAP-TEAD来抑制扩散.
  • VGLL4对于这些化合物的抗增殖作用至关重要.
  • 过度表达VGLL4使细胞对这些化合物敏感,而删除则消除了敏感性.

结论:

  • 一个新的TEAD抑制剂类别作为"分子剂",促进VGLL4-TEAD相互作用.
  • 这种机制提供了一种新的策略来抵消瘤性河马通路信号.
  • 这些发现有助于进一步了解TEAD向的癌症疗法.