Investigation Role of Toll-like Receptor-9 Gene and miR-155 Expression Levels in Acute Myeloid Leukemia via Quantitative Real-Time PCR.

Q2 Medicine
Maryam Qasim Mohammed, Amal Mohammed Ali, Ali Hussein Alwan, Ahmed Mahdi Hamzah, Zainab Saad Azeez Al-Musawi
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引用次数: 0

Abstract

Objective: This study aims to investigate the mRNA expression levels of Toll-like receptor 9 and microRNA-155 in Iraqi patients diagnosed with acute myeloid leukemia (AML) within a case-control study framework. Additionally, the study will assess relevant hematological parameters.

Methods: This study enrolled 40 Iraqi patients diagnosed with AML who were undergoing chemotherapy and experiencing relapse, and 40 healthy individuals as a control group. Hematological parameters were measured using a complete blood count (CBC) device. RNA was extracted from samples, quantified, and assessed for purity. Subsequently, RNA was reverse-transcribed into complementary DNA (cDNA). The relative expression levels of TLR-9 and miR-155 genes were quantified using quantitative real-time polymerase chain reaction (qRT-PCR).

Result: Hemoglobin, erythrocyte, hematocrit, and platelet levels exhibited significant differences between AML patients and healthy controls. In contrast, white blood cell and lymphocyte counts were not significantly different between the two groups. TLR-9 gene expression was comparable between healthy controls and AML patients, with fold change values of 1.000 and 1.49, respectively. However, miR-155 expression was significantly lower in AML patients compared to healthy controls, with fold change values of 0.608 and 1.000, respectively.

Conclusion: To evade host immune surveillance, cancer cells may downregulate the expression of TLR-9 and miR-155. This dysregulation may contribute to the progression and development of AML. Furthermore, the downregulation of miR-155 and dysregulation of TLR-9 during oncogenesis may serve as potential prognostic markers for AML patients.

toll样受体9基因和miR-155表达水平在急性髓系白血病中的作用
目的:在病例对照研究框架下,研究伊拉克急性髓性白血病(AML)患者toll样受体9和microRNA-155的mRNA表达水平。此外,该研究将评估相关血液学参数。方法:本研究招募了40名正在接受化疗和复发的伊拉克AML患者,以及40名健康个体作为对照组。使用全血细胞计数(CBC)装置测量血液学参数。从样品中提取RNA,定量并评估纯度。随后,RNA被逆转录成互补DNA (cDNA)。采用实时定量聚合酶链式反应(qRT-PCR)定量检测TLR-9和miR-155基因的相对表达水平。结果:AML患者血红蛋白、红细胞、红细胞压积和血小板水平与健康对照组有显著差异。相比之下,白细胞和淋巴细胞计数在两组之间无显著差异。TLR-9基因表达在健康对照组和AML患者之间具有可比性,其倍数变化值分别为1.000和1.49。然而,与健康对照组相比,AML患者中miR-155的表达明显降低,其倍数变化值分别为0.608和1.000。结论:为了逃避宿主免疫监视,癌细胞可能下调TLR-9和miR-155的表达。这种失调可能有助于AML的进展和发展。此外,在肿瘤发生过程中miR-155的下调和TLR-9的失调可能是AML患者的潜在预后标志物。
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来源期刊
CiteScore
2.80
自引率
0.00%
发文量
779
审稿时长
3 months
期刊介绍: Cancer is a very complex disease. While many aspects of carcinoge-nesis and oncogenesis are known, cancer control and prevention at the community level is however still in its infancy. Much more work needs to be done and many more steps need to be taken before effective strategies are developed. The multidisciplinary approaches and efforts to understand and control cancer in an effective and efficient manner, require highly trained scientists in all branches of the cancer sciences, from cellular and molecular aspects to patient care and palliation. The Asia Pacific Organization for Cancer Prevention (APOCP) and its official publication, the Asia Pacific Journal of Cancer Prevention (APJCP), have served the community of cancer scientists very well and intends to continue to serve in this capacity to the best of its abilities. One of the objectives of the APOCP is to provide all relevant and current scientific information on the whole spectrum of cancer sciences. They aim to do this by providing a forum for communication and propagation of original and innovative research findings that have relevance to understanding the etiology, progression, treatment, and survival of patients, through their journal. The APJCP with its distinguished, diverse, and Asia-wide team of editors, reviewers, and readers, ensure the highest standards of research communication within the cancer sciences community across Asia as well as globally. The APJCP publishes original research results under the following categories: -Epidemiology, detection and screening. -Cellular research and bio-markers. -Identification of bio-targets and agents with novel mechanisms of action. -Optimal clinical use of existing anti-cancer agents, including combination therapies. -Radiation and surgery. -Palliative care. -Patient adherence, quality of life, satisfaction. -Health economic evaluations.
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