Revealing of TLR-9 gene polymorphisms by qPCR HRM technique and their influence on TLR-9 serum level in acute myeloid leukemia patients: Case-control study

IF 3.7 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Cytokine Pub Date : 2024-08-11 DOI:10.1016/j.cyto.2024.156730
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Abstract

Acute myeloid leukemia (AML) is one of the most common and fatal malignancies that affect adults, which can quickly become aggressive if left untreated, and leukemia cells invade the bone marrow. TLR-9 is an innate immune cell receptor sensitive to various PAMPs and encoded by the TLR-9 gene. As is often known, genetic polymorphisms in any gene can help the development of the disease, and these three polymorphisms, rs187084, rs5743836, and rs352140 of TLR-9, have been studied in many different cancer disorders. Therefore, this study aimed to discover the multiple forms of a TLR-9 gene in a sample of Iraqi AML patients. A total of 120 participants in a case-control study were enrolled in the current study. Using CBC, some hematological parameters were evaluated, and the serum level of TLR-9 was assessed using the ELISA technique. DNA was extracted directly from blood, and a high-resolution melting (HRM) analysis was then carried out. The results revealed a significant difference in some blood parameters among patients and healthy control, while WBC and lymphocytes were without an evident difference between the two groups of the current investigation. The serum concentration of TLR-9 showed an elevated level in patients (P value < 0.01). Nonetheless, this increase was not affected by the genotype patterns of polymorphisms. According to the P-value, there was a significant difference in wild genotypes of the three polymorphisms (rs187084, rs5743836, and rs352140). At the same time, the odds ratio revealed the association with the disease as a protective factor. In contrast, there was a significant difference in the heterozygous and mutant genotypes of TLR-9 polymorphisms, though the odds ratio confirmed the association with the AML as a risk factor. The results of rs352140 were compatible with H.W.E since there were no significant differences between the observed and expected values for either patients or healthy controls. In contrast, the result of rs5743836 was not consistent with the HWE. Furthermore, although it corresponds with the healthy one, the finding of rs187084 conflicted with H.W.E. in the patient group. In conclusion, High serum levels of TLR-9 in patients could act as biomarkers for AML. The TLR-9 gene polymorphisms (rs187084, rs5743836, and rs352140) have been linked to an increased risk of AML and may impact the disease progression in the Iraqi population.

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利用 qPCR HRM 技术揭示急性髓性白血病患者的 TLR-9 基因多态性及其对 TLR-9 血清水平的影响:病例对照研究
急性髓性白血病(AML)是影响成年人的最常见、最致命的恶性肿瘤之一,如果不及时治疗,白血病细胞侵入骨髓后会迅速发展为侵袭性白血病。TLR-9 是一种对各种 PAMPs 敏感的先天性免疫细胞受体,由 TLR-9 基因编码。众所周知,任何基因的遗传多态性都有助于疾病的发展,而 TLR-9 的 rs187084、rs5743836 和 rs352140 这三个多态性已在许多不同的癌症疾病中被研究过。因此,本研究旨在发现伊拉克急性髓细胞性白血病患者样本中 TLR-9 基因的多种形式。本研究共招募了 120 名病例对照研究参与者。通过全血细胞计数,对一些血液学参数进行了评估,并使用 ELISA 技术对血清中的 TLR-9 水平进行了评估。直接从血液中提取 DNA,然后进行高分辨率熔解(HRM)分析。结果显示,患者和健康对照组的部分血液参数存在明显差异,而白细胞和淋巴细胞在本次调查的两组之间没有明显差异。患者血清中的 TLR-9 浓度升高(P 值为 0.01)。然而,这种升高并不受多态性基因型模式的影响。根据 P 值,三种多态性(rs187084、rs5743836 和 rs352140)的野生基因型存在显著差异。同时,几率比显示,该多态性与该疾病相关,是一种保护性因素。相比之下,TLR-9 多态性的杂合基因型和突变基因型存在显著差异,尽管几率比证实与急性髓细胞白血病的关联是一个危险因素。rs352140的结果与H.W.E相符,因为无论是患者还是健康对照组,观察值和预期值之间都没有显著差异。相比之下,rs5743836 的结果与 HWE 不一致。此外,虽然 rs187084 的结果与健康对照组一致,但在患者组中却与 H.W.E. 相冲突。总之,患者血清中高水平的 TLR-9 可作为急性髓细胞性白血病的生物标志物。TLR-9基因多态性(rs187084、rs5743836和rs352140)与罹患急性髓细胞性白血病的风险增加有关,可能会影响伊拉克人群的病情发展。
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来源期刊
Cytokine
Cytokine 医学-免疫学
CiteScore
7.60
自引率
2.60%
发文量
262
审稿时长
48 days
期刊介绍: The journal Cytokine has an open access mirror journal Cytokine: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. * Devoted exclusively to the study of the molecular biology, genetics, biochemistry, immunology, genome-wide association studies, pathobiology, diagnostic and clinical applications of all known interleukins, hematopoietic factors, growth factors, cytotoxins, interferons, new cytokines, and chemokines, Cytokine provides comprehensive coverage of cytokines and their mechanisms of actions, 12 times a year by publishing original high quality refereed scientific papers from prominent investigators in both the academic and industrial sectors. We will publish 3 major types of manuscripts: 1) Original manuscripts describing research results. 2) Basic and clinical reviews describing cytokine actions and regulation. 3) Short commentaries/perspectives on recently published aspects of cytokines, pathogenesis and clinical results.
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