瘤XPA变异导致NER中的缺陷,使细胞对思柏敏感
Alexandra M Blee1,2, Kaitlyn S Gallagher1,2, Hyun-Suk Kim3
1Department of Biochemistry, Vanderbilt University, Nashville, TN 37205, USA.
NAR cancer
|March 19, 2024
概括
在Xeroderma Pigmentosum补充组A (XPA) 中的瘤突变可以通过损害DNA修复来降低基于的化疗的有效性. 了解这些XPA变异对于预测患者对化疗反应至关重要.
科学领域:
- 分子生物学分子生物学
- 遗传学 遗传学 是一个
- 癌症研究 癌症研究
背景情况:
- 核酸切除修复 (NER) 消除了的DNA病变,降低了化疗的疗效.
- 像ERCC1和ERCC2这样的NER基因突变改善了用化疗治疗患者的结果.
- 其他NER基因突变对化疗反应的影响在很大程度上是未知的.
研究的目的:
- 研究Xeroderma Pigmentosum补充组A (XPA) 基因中的遗传变异对DNA修复和化疗敏感性的功能影响.
- 用体外和基于细胞的测试分析预测的XPA变体,以了解它们的NER功能障碍机制.
主要方法:
- 机器学习被用来预测XPA的DNA修复破坏变体.
- 在体外分析纯化重组XPA蛋白.
- 基于细胞的测试来评估剂的敏感性和NER功能障碍机制.
主要成果:
- 在XPA变种Y148D中,NER缺陷显著减少.
- 这种变体显示蛋白质稳定性下降,DNA结合受损,并破坏了DNA损伤部位的招募.
- XPA Y148D 变异导致对西斯治疗和细胞降解的敏感性增加.
结论:
- 在XPA中发生的瘤特异性突变会影响西斯治疗后的细胞存活率.
- 这些发现提供了对NER功能障碍的机制性见解,并改善了变异效应预测.
- 在预测患者对基化疗的反应时,应考虑XPA瘤变异.
相关概念视频
Nucleotide Excision Repair
3.5K
DNA Distortion and Damage
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
3.5K
Abnormal Proliferation
4.5K
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
4.5K
Long-patch Base Excision Repair
7.0K
Since the discovery of the two BER pathways, there has been a debate about how a cell chooses one pathway over the other and the factors determining this selection. Numerous in vitro experiments have pointed out multiple determinants for the sub-pathway selection. These are:
7.0K
Treatment Resistant Cancers
3.3K
Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
3.3K
The Intrinsic Apoptotic Pathway
6.5K
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...
6.5K
Base Excision Repair
22.3K
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...
22.3K


