Dogru Gurbet, Ay Ozlem Izci, Erdal Mehmet Emin, Ay Mustafa Ertan, Tombak Anıl, Karakas Umit
Department of Medical Biology and Genetics, Faculty of Medicine, Mersin University, Mersin, Turkey.
Department of Heamatology, Faculty of Medicine, Mersin University, Mersin, Turkey.
Adv Clin Exp Med. 2017 Aug;26(5):761-765. doi: 10.17219/acem/63087.
Polycythemia vera (PV) and essential thrombocytosis (ET) are hematological disorders characterized by excessive production of mature and functional blood cells. These cellular disorders are thought to be associated with impaired apoptosis, which is one of the major cellular death mechanisms in hematopoietic cells.
In this study, our objective was to examine the association between potential polymorphisms of the Bcl 2, Bax, Fas and Fas Ligand genes involved in apoptosis and the occurrence of PV and ET.
A total of 93 patients diagnosed with PV (n = 38) or ET (n = 55) at the Department of Hematology were included in this study, and 93 healthy individuals served as controls. DNA isolation was performed in blood samples obtained from both groups of subjects to determine the Bcl 2, Bax, Fas, and Fas L genotypes using the real-time PCR method.
No statistically significant differences between controls and patients were found in terms of Fas -670 G > A (rs1800682), Fas -1377 G > A (rs2234767), Fas L IVS2 -124 A > G (rs5030772), Bax -248 G > A (rs4645878) and Bcl 2 -938 C > A (rs2279115) polymorphisms, genotypes, and allele frequency (p > 0.05).
The results show that polymorphisms in the Bcl 2, Bax, Fas, and Fas Ligand genes involved in the apoptotic pathways may not play a role in the pathogenesis of PV and ET.
真性红细胞增多症(PV)和原发性血小板增多症(ET)是血液系统疾病,其特征是成熟且功能正常的血细胞过度生成。这些细胞紊乱被认为与凋亡受损有关,而凋亡是造血细胞主要的细胞死亡机制之一。
在本研究中,我们的目的是检测参与凋亡的Bcl 2、Bax、Fas和Fas配体基因的潜在多态性与PV和ET发生之间的关联。
本研究纳入了血液科诊断为PV(n = 38)或ET(n = 55)的93例患者,93名健康个体作为对照。从两组受试者采集的血液样本中进行DNA分离,采用实时PCR方法确定Bcl 2、Bax、Fas和Fas L基因型。
在Fas -670 G > A(rs1800682)、Fas -1377 G > A(rs2234767)、Fas L IVS2 -124 A > G(rs5030772)、Bax -248 G > A(rs4645878)和Bcl 2 -938 C > A(rs2279115)多态性、基因型及等位基因频率方面,对照组与患者之间未发现统计学显著差异(p > 0.05)。
结果表明,参与凋亡途径的Bcl 2、Bax、Fas和Fas配体基因多态性可能在PV和ET的发病机制中不起作用。