一个紧的合成途径将癌症信号重新连接到治疗效应器释放
Hokyung K Chung1,2,3, Xinzhi Zou4, Bryce T Bajar3,4
1Department of Biology, Stanford University, Stanford, CA, USA.
概括
合成生物学可以将异常信号重新连接到效应器释放 (RASER),以向癌细胞. 这种方法采用瘤性ErbB活性来触发治疗方案,选择性地切除癌细胞.
科学领域:
- 合成生物学
- 分子医学
- 生物化学
背景情况:
- 针对癌细胞仍然是分子医学中的一个挑战.
- 目前的治疗常常会抑制致癌途径, 但需要新的方法.
- 工程生化途径对于解决生物医学问题至关重要.
研究的目的:
- 开发一种用于特定识别和切除癌细胞的新方法.
- 设计一个能将致癌状态与治疗结果联系起来的系统.
- 创建基于异常信号的癌症向策略.
主要方法:
- 开发了对效应器释放 (RASER) 系统的异常信号的重新布线.
- 整合瘤ErbB受体活动以触发治疗方案.
- 使用数学建模进行理性优化和输出编程.
- 在癌细胞中诱导了亡和CRISPR- Cas9介导的转录.
主要成果:
- RASER特别将ErbB过度活跃与亡等期望结果联系在一起.
- 选择性废除的ErbB过活性的癌细胞的腺相关病毒输送.
- 节省了ErbB正常细胞,显示出高特异性.
- 在癌细胞中证明成功的内源基因CRISPR- Cas9介导转录.
结论:
- RASER为癌基因特异性癌症的检测和治疗提供了一种新策略.
- 该系统提供了一种用于治疗目的的异常信号的方法.
- 这种方法促进了合成生物学在分子医学中的应用.
更多相关视频
相关概念视频
Interactions Between Signaling Pathways
7.3K
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...
7.3K
Notch Signaling Pathway
6.5K
The Notch signaling pathway is a major intracellular signaling pathway that is highly conserved over a broad spectrum of metazoan species. It stands unique from other intracellular signaling mechanisms in animals because notch protein itself acts as the receptor as well as the primary signaling molecule.
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not...
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not...
6.5K
Hedgehog Signaling Pathway
9.9K
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...
9.9K
Insulin: The Receptor and Signaling Pathways
2.9K
Insulin action is mediated through a receptor tyrosine kinase, akin to the IGF-1 receptor. The number of receptors per cell varies significantly, from 40 on erythrocytes to 300,000 on adipocytes and hepatocytes. The insulin receptor consists of linked α/β subunit dimers, forming a heterotetramer glycoprotein with two extracellular α subunits and two β subunits spanning the membrane. The α subunits inhibit the inherent tyrosine kinase activity of the β subunits, but...
2.9K
IP3/DAG Signaling Pathway
14.4K
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...
14.4K
Nitric Oxide Signaling Pathway
6.2K
Nitric oxide (NO), an inorganic gas, acts as a potent second messenger in most animal and plant tissues. NO diffuses out of the cells that produce it and enters the neighboring cells to generate a downstream response. NO synthase (NOS) catalyzes NO production by the deamination of the amino acid arginine. There are three isoforms of NOS. Endothelial cells have endothelial NOS (eNOS), nerve and muscle cells have neuronal NOS (nNOS), and macrophages produce inducible NOS (iNOS) upon exposure...
6.2K


