Alnaqashli Yusur Ridha, Jasim Hameed Majeed
College of Biotechnology, Al-Nahrain University, Baghdad, Iraq.
Asian Pac J Cancer Prev. 2024 Dec 1;25(12):4223-4227. doi: 10.31557/APJCP.2024.25.12.4223.
Acute myeloid leukemia (AML) is a hematological malignancy marked by the abnormal proliferation of myeloid precursor cells (blasts) in the bone marrow and peripheral blood, leading to disrupted blood cell production. The telomerase reverse transcriptase (hTERT), a key component of the telomerase enzyme, is often overexpressed in various cancers, including AML, contributing to cellular immortality. This study aimed to investigate the expression levels of the hTERT gene, serum protein concentrations, and hematological parameters in newly diagnosed AML patients, comparing these findings to AML patients in remission and healthy controls.
Blood samples were collected from three groups: 10 newly diagnosed AML patients, 35 AML patients in remission, and 40 healthy controls. Hematological parameters, including white blood cell (WBC), red blood cell (RBC), platelet (PLT), and hemoglobin (Hb) levels, were measured. Serum hTERT protein concentrations were analyzed using enzyme-linked immunosorbent assay (ELISA), and hTERT gene expression was assessed through reverse transcription-quantitative PCR (RT-qPCR).
The study demonstrated that newly diagnosed AML patients had significantly higher hTERT gene expression and serum protein levels compared to both remission patients and healthy individuals. Hematological analyses revealed elevated WBC counts alongside reduced RBC, PLT, and Hb levels in AML patients relative to controls.
Increased hTERT expression and serum protein levels are valuable biomarkers for diagnosing and monitoring AML. These findings highlight the therapeutic potential of targeting hTERT and underscore the importance of conducting further studies on larger patient cohorts to validate these results.
急性髓系白血病(AML)是一种血液系统恶性肿瘤,其特征是骨髓和外周血中髓系前体细胞(原始细胞)异常增殖,导致血细胞生成紊乱。端粒酶逆转录酶(hTERT)是端粒酶的关键组成部分,在包括AML在内的多种癌症中常过度表达,促成细胞永生化。本研究旨在调查新诊断AML患者的hTERT基因表达水平、血清蛋白浓度和血液学参数,并将这些结果与缓解期AML患者及健康对照进行比较。
从三组人群中采集血样:10例新诊断的AML患者、35例缓解期AML患者和40例健康对照。测量血液学参数,包括白细胞(WBC)、红细胞(RBC)、血小板(PLT)和血红蛋白(Hb)水平。使用酶联免疫吸附测定(ELISA)分析血清hTERT蛋白浓度,并通过逆转录定量PCR(RT-qPCR)评估hTERT基因表达。
研究表明,与缓解期患者和健康个体相比,新诊断的AML患者的hTERT基因表达和血清蛋白水平显著更高。血液学分析显示,与对照组相比,AML患者的白细胞计数升高,同时红细胞、血小板和血红蛋白水平降低。
hTERT表达增加和血清蛋白水平升高是诊断和监测AML的有价值生物标志物。这些发现突出了靶向hTERT的治疗潜力,并强调了对更大患者队列进行进一步研究以验证这些结果的重要性。