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相关概念视频

Mitogens and the Cell Cycle02:38

Mitogens and the Cell Cycle

Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...
The Ras Gene02:38

The Ras Gene

The Ras-gene-encoded proteins are regulators of signaling pathways controlling cell proliferation, differentiation, or cell survival. The Ras-gene family in humans constitutes three primary members—the HRas, NRas, and KRas. These genes code for four functionally distinct yet closely related proteins—the HRas, NRas, KRas4A, and KRas4B. The involvement of mutant Ras genes in human cancer was first discovered in 1982 and is among the most common causes of human tumorigenesis.
Ras is a superfamily...
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

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...
IP3/DAG Signaling Pathway01:11

IP3/DAG Signaling Pathway

Membrane lipids such as phosphatidylinositol (PI) are precursors for several membrane-bound and soluble second messengers. Specific kinases phosphorylate PI and produce phosphorylated inositol phospholipids. One such inositol phospholipids are the  phosphatidylinositol-4,5 bisphosphate [PI(4,5)P2], present in the inner half of the lipid bilayer. Upon ligand binding, GPCR stimulates Gq proteins to turn on phospholipase Cꞵ. Activated phospholipase Cꞵ cleaves PI(4,5)P2 and produces two-second...
Intracellular Signaling Affects Focal Adhesions01:17

Intracellular Signaling Affects Focal Adhesions

Integrins act both as extracellular input receivers and as intracellular processing activators. As their name suggests, integrins are entirely integrated into the membrane structure. Their hydrophobic membrane-spanning regions interact with the phospholipid bilayer's hydrophobic region. These membrane receptors provide extracellular attachment sites for effectors like hormones and growth factors. They activate intracellular response cascades when their effectors are bound and active.
Some...
Chronic Pancreatitis I: Introduction01:25

Chronic Pancreatitis I: Introduction

Chronic pancreatitis is a long-standing, relapsing inflammation of the pancreas, characterized by irreversible damage to the gland. It results in progressive destruction of the pancreatic parenchyma, fibrosis, and eventual loss of both exocrine and endocrine function. The disease may evolve gradually after multiple episodes of acute pancreatitis or develop independently.EtiologyChronic pancreatitis can arise from a variety of causes:Alcohol use is the leading cause, accounting for 70–80% of...

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Enhancement of Apoptotic and Autophagic Induction by a Novel Synthetic C-1 Analogue of 7-deoxypancratistatin in Human Breast Adenocarcinoma and Neuroblastoma Cells with Tamoxifen
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PAR1是一种矩阵金属蛋白酶-1受体,促进乳腺癌细胞的入侵和瘤发生.

Adrienne Boire1, Lidija Covic, Anika Agarwal

  • 1Molecular Oncology Research Institute, Tufts-New England Medical Center, Boston, Massachusetts 02111, USA.

Cell
|February 15, 2005
PubMed
概括

矩阵金属蛋白酶-1 (MMP-1) 在乳腺癌中激活蛋白酶激活受体-1 (PAR1). 这种相互作用促进了瘤微环境中的癌细胞入侵和转移.

科学领域:

  • 在瘤学瘤学.
  • 分子生物学分子生物学
  • 生物化学 生物化学

背景情况:

  • 蛋白酶激活受体 (PAR) 是G蛋白合受体,在血栓形成,炎症和血管生物学中至关重要.
  • PAR1与癌症侵袭和转移有关,但激活蛋白酶是未知的.

研究的目的:

  • 为了识别乳腺癌侵袭中激活PAR1的蛋白酶.
  • 研究PAR1及其激活蛋白酶在乳腺癌细胞生长和侵入中的作用.

主要方法:

  • 利用异种移植模型评估PAR1在乳腺癌细胞生长和侵入中的作用.
  • 研究了矩阵金属蛋白酶-1 (MMP-1) 和 PAR1.1 之间的相互作用.
  • 分析了MMP-1在癌细胞和纤维细胞中的活性.

主要成果:

  • 在体内促进乳腺癌细胞生长和侵入的过程中,PAR1的表达是必要和足够的.
  • 矩阵金属蛋白酶-1 (MMP-1) 作为PAR1的蛋白酶激动剂,分裂它以诱导信号和迁移.
  • MMP-1起源于脑膜纤维细胞,而不是癌细胞本身.

结论:

  • 在瘤微环境中的MMP-1在乳腺癌细胞上激活PAR1.

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  • 这种MMP-1/PAR1轴促进癌细胞迁移和入侵,突出了瘤进展的关键机制.