Bcl-xL脱化是调节对DNA损伤反应的关键开关
Benjamin E Deverman1, Brian L Cook, Scott R Manson
1Division of Urology, Department of Cell Biology and Physiology, School of Medicine, Washington University, 660 South Euclid Avenue, Campus Box 8052, Saint Louis, MO 63110, USA.
Cell
|October 10, 2002
概括
破坏DNA的癌症药物通过在瘤细胞中去amidatingBcl-xL引发细胞亡,但不是正常细胞. 这种脱氧化使瘤细胞易受亡,突出了癌症治疗中的关键机制.
科学领域:
- 分子生物学分子生物学
- 癌症研究 癌症研究
- 细胞生物学 细胞生物学
背景情况:
- 破坏DNA的抗瘤剂的治疗疗效依赖于选择性瘤细胞亡.
- 了解差异性亡诱导机制对于癌症治疗至关重要.
研究的目的:
- 研究Bcl-xL脱化在对DNA损伤剂的差异性亡反应中的作用.
- 阐明Bcl-xL脱化影响亡易感性的机制.
主要方法:
- 在各种瘤细胞系和纤维细胞中分析Bcl-xL脱化.
- 在DNA损伤后诱导亡的评估.
- 研究Bcl-xL和仅BH3域蛋白之间的相互作用.
主要成果:
- 在Bcl-xL的非结构循环中,两个阿斯巴拉金的脱化被确定为瘤细胞中关键的亡反应.
- Bcl-xL脱胺破坏了它的功能,通过损害对前性BH3蛋白的抑制,增加了对亡的易感性.
- 纤维细胞积极抑制Bcl-xL脱化,有助于它们抵抗DNA损伤诱导的亡.
结论:
- 调节Bcl-xL脱化对于破坏DNA的抗瘤剂对瘤特异性的影响至关重要.
- 准Bcl-xL脱氧化途径可能为增强癌症治疗提供新的策略.
相关概念视频
Overview of DNA Repair
In order to be passed through generations, genomic DNA must be undamaged and error-free. However, every day, DNA in a cell undergoes several thousand to a million damaging events by natural causes and external factors. Ionizing radiation such as UV rays, free radicals produced during cellular respiration, and hydrolytic damage from metabolic reactions can alter the structure of DNA. Damages caused include single-base alteration, base dimerization, chain breaks, and cross-linkage.
Chemically...
Chemically...
Base Excision Repair
One of the common DNA damages is the chemical alteration of single bases by alkylation, oxidation, or deamination. The altered bases cause mispairing and strand breakage during replication. This type of damage causes minimal change to the DNA double helix structure and can be repaired by the base excision repair (BER) pathways. BER corrects damaged DNA sequences by removing the damaged base and restoring the original base sequence using the complementary strand as a template.
The first step of...
The first step of...
Fixing Double-strand Breaks
The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
DNA Damage can Stall the Cell Cycle
In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
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Internal cellular stress, such as cellular injury or hypoxia, triggers intrinsic apoptosis. The B-cell lymphoma 2 (Bcl-2) family of proteins are the primary regulators of the intrinsic apoptotic pathway. For example, during DNA damage, checkpoint proteins, such as Ataxia Telangiectasia Mutated (ATM protein) and Checkpoints Factor-2 (Chk2) proteins, are activated. These proteins phosphorylate p53 which further activates pro-apoptotic proteins, such as Bax, Bak, PUMA, and Noxa, and inhibits...
DNA Damage Can Stall the Cell Cycle
In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...


