一个主要的长性下骨肉瘤与生殖线恶性疾病相关的DNA损伤修复基因多态:一个案例报告
Muhammad Tahir1, Eric X Wei1, Carlina Madelaire1
1Department of Pathology University of South Alabama, 2451 University Hospital Drive, Mobile, Alabama 36617, USA.
Case reports in oncological medicine
|July 4, 2024
概括
这项研究详细介绍了一位81岁的老妇人罕见的下骨髓骨质肉瘤. 基因分析揭示了DNA修复和亡基因的突变,表明与遗传癌症风险因素的联系.
科学领域:
- 在瘤学瘤学.
- 遗传学 遗传学 是一个
- 口腔病理学 口腔病理学
背景情况:
- 主要下带切口性骨髓瘤异常罕见,报告的病例有限.
- 这些瘤的特点是囊性,充满血液的腔和由高等级恶性细胞线的瘤骨.
研究的目的:
- 报道了第一个全外体DNA测序分析初级下骨髓骨髓瘤的第一个全外体DNA测序分析.
- 为了研究与这种罕见的下瘤相关的分子基础和遗传变异.
- 探索已识别的基因多态和家族癌症发病率之间的潜在联系.
主要方法:
- 对手术切除下质量的组织学检查.
- 结合瘤和良性DNA的全外体DNA测序.
- 对比测序数据分析以识别瘤特异变体和共享多态.
主要成果:
- 鉴定了瘤DNA独特的1577种变异,这些变异聚集在调节DNA修复和亡的基因中.
- 发现了与癌症风险增加相关的共享基因多态 (例如,ATM,p53,BRCA1,BRCA2).
- 识别的多形态与异常高癌症发病率的家族史的相关性.
结论:
- 这项研究提供了第一个基因组洞察 mandibular telangiectatic骨髓瘤.
- 研究结果表明,遗传的癌症风险多态可能有助于这些罕见的下瘤的发展.
- 分子数据可能会阐明这种罕见瘤的病原体及其潜在的遗传影响.
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
Base Excision Repair
22.2K
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...
22.2K
Mismatch Repair
4.8K
Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
4.8K
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
Fixing Double-strand Breaks
12.5K
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...
12.5K
DNA Damage can Stall the Cell Cycle
9.1K
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...
9.1K


