宫癌相关静脉血栓的血静基因变异:临床策略的考虑因素
Beatriz Vieira Neto1,2, Valéria Tavares1,3,4, José Brito da Silva5
1Molecular Oncology and Viral Pathology Group, Research Center of IPO Porto (CI-IPOP)/Pathology and Laboratory Medicine Dep, Clinical Pathology SV/ RISE@CI-IPOP (Health Research Network), Portuguese Oncology Institute of Porto (IPO Porto) / Porto Comprehensive Cancer Centre (Porto.CCC), Porto, 4200-072, Portugal.
Journal of thrombosis and thrombolysis
|April 20, 2024
概括
在SERPINE1和F2基因中的单核酸多态 (SNP) 可以帮助预测静脉血栓塞栓症 (VTE) 风险和接受化疗或放射治疗的宫癌患者的整体存活率.
科学领域:
- 在瘤学瘤学.
- 遗传学 遗传学 是一个
- 血液学 血液学 血液学
背景情况:
- 静脉血栓栓塞 (VTE) 是癌症患者的严重并发症,特别是那些接受化疗或放射治疗的宫癌患者.
- 目前的风险评估模型,如Khorana评分,在预测该群体的VTE方面表现有限.
- 血液静止基因中的单核酸多态 (SNP) 正在被研究为癌症相关血栓形成 (CAT) 的潜在生物标志物.
研究的目的:
- 调查特定的静血基因SNP在CC患者中对VTE的预测能力.
- 为了探索这些SNP的预后价值关于整体存活率 (OS),独立于VTE.
- 为了确定新的生物标志物,以改善血栓预防和管理策略在CC.
主要方法:
- 一项回顾性队列研究,涉及401名接受化疗或放射治疗的CC患者.
- 在静血基因中评估六个SNP,重点关注SERPINE1 rs2070682和F2 rs1799963.
- 评估SNP之间的关联,VTE发生的时间和整体存活率,使用日志等级测试和Cox模型.
主要成果:
- 与癌症相关的血栓形成 (CAT) 显著影响了CC患者的整体存活 (OS) (P < 0.001).
- SERPINE1 rs2070682多态性与CC相关的VTE风险增加显著相关 (基因型P=0.002,HR=6.99,等位基因P=0.009).
- F2 rs1799963多态表现为OS的显著预后值,不论VTE (P = 0.020的基因型,HR = 2.76,P = 0.026的等位基因).
结论:
- SERPINE1 rs2070682 SNP可以作为一种有价值的生物标志物,用于预测CC患者的静脉瘤风险.
- F2 rs1799963 SNP证明了对CC患者整体存活期的预后意义.
- 这些遗传多态性可能有助于临床决策,用于血栓预防和血栓塞瘤管理.
相关概念视频
Anticoagulant Drugs: Low-Molecular-Weight Heparins
689
Hemostasis is a crucial process that prevents excessive blood loss from damaged blood vessels. It involves various mechanisms such as vasoconstriction, platelet adhesion and activation, and fibrin formation. The importance of each mechanism depends on the type of vessel injury. In contrast, thrombosis is the abnormal formation of a blood clot within the blood vessels, leading to potential complications if the clot obstructs blood flow. Thrombosis can be caused by increased coagulability of the...
689
Disorders of Hemostasis
881
Hemostasis, the process that stops bleeding after a blood vessel injury, is crucial for maintaining the integrity of the circulatory system. However, disorders of hemostasis can disrupt this delicate balance, leading to either excessive clotting or bleeding. These disorders can be broadly classified into thromboembolic disorders and bleeding disorders.
Thromboembolic Disorders
Two factors primarily cause thromboembolic conditions.
Thromboembolic Disorders
Two factors primarily cause thromboembolic conditions.
881
Esophageal Varices-II: Clinical Features and Management
60
Esophageal varices often manifest as gastrointestinal bleeding episodes, presenting symptoms like hematemesis (vomiting of blood), hematochezia (passing fresh blood via the rectum), and melena (black, tarry stools). Other signs can include weight loss, anorexia, abdominal discomfort, jaundice, pruritus, altered mental status, and muscle cramps.
In the initial assessment, a thorough review of the patient's medical history is vital to identify risk factors such as liver disease, alcohol...
In the initial assessment, a thorough review of the patient's medical history is vital to identify risk factors such as liver disease, alcohol...
60
Regulation of Angiogenesis and Blood Supply
2.6K
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...
2.6K
Comparing Copy Number Variations and SNPs
17.7K
Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
17.7K
Histone Variants at the Centromere
4.3K
Histone variants are the histone proteins with structural and sequence variations. These variants may be regarded as “mutant” forms that replace their canonical histone counterparts in the nucleosomes. Specific post-translational modifications on the histone variants enable further chromatin complexity and regulate tissue-specific gene expression. The most common histone variants are from histone H2A, H2B, and linker histone H1 families. However, several variants of histone H3...
4.3K


