蛇毒素促进癌细胞存活和血管合作在大脑转移
Manuel Valiente1, Anna C Obenauf1, Xin Jin1
1Cancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Cell
|March 4, 2014
概括
大脑是大脑的大脑.
科学领域:
- 在瘤学瘤学.
- 神经科学是一个神经科学.
- 生物化学 生物化学
背景情况:
- 大脑转移是癌症的严重并发症,癌细胞死亡的机制尚不清楚.
- 入大脑的癌细胞面临着未知的因素,这通常会导致它们的死亡.
研究的目的:
- 为了确定大脑对转移性癌细胞的防御机制.
- 阐明塑原激活剂 (PA) 抑制蛇形在脑转移期间癌细胞中的作用.
主要方法:
- 研究了脑筋膜瘤成分与透的癌细胞之间的相互作用.
- 分析了肺癌和乳腺癌中大脑转移细胞中蛇的表达.
- 研究了等离子素对大脑微环境中的星细胞FasL和L1CAM的影响.
主要成果:
- 血,来自大脑层,作为对大脑转移的防御作用.
- 等离子素通过诱导癌细胞通过天体细胞FasL死亡,并通过抑制L1CAM介导的扩散来抑制转移.
- 癌细胞表达抗PA蛇形蛋白 (神经蛇形蛋白,蛇形蛋白B2),以逃避等离子素的抑制作用.
- 抗PA蛇保护癌细胞免受死亡信号的影响,并促进血管合作,促进大脑转移.
结论:
- 等离子素是大脑对癌症转移的天生的防御的一个关键组成部分.
- 癌细胞利用抗PA蛇作为一个盾牌,以克服等离子体介导的抑制.
- 这种机制为肺癌和乳腺癌中大脑转移的启动提供了统一的解释.
相关概念视频
Metastasis
5.4K
Metastasis is the spread of cancer cells from the original site to distant locations in the body. Cancer cells can spread via blood vessels (hematogenous) as well as lymph vessels in the body.
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
5.4K
Selectins
3.6K
Cell adhesion is an essential aspect of multicellularity. While stable cell interactions usually occur between cells of the same type, transient cell interactions occur between cells of different tissue types, such as between neutrophils and endothelial cells. Selectins are one class of cell adhesion molecules (CAMs) that bind carbohydrate ligands to form transient cell adhesion. They are rod-like proteins with a long extracellular part of variable length ending with the lectin domain,...
3.6K
Adaptive Mechanisms in Cancer Cells
5.7K
Cancer cells accumulate genetic changes at an abnormally rapid rate due to the defects in the DNA repair mechanisms. From an evolutionary perspective, such genetic instability is advantageous for cancer development. Mutant cell lines accumulate a series of beneficial mutations that contribute to their progression into cancer.
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
5.7K
Regulation of Angiogenesis and Blood Supply
2.9K
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...
2.9K
Mitogens and the Cell Cycle
6.3K
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...
6.3K
The Tumor Microenvironment
6.3K
Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
6.3K


