与正常组相比,HTLV-1 衍生的成人 T 细胞白血病/淋巴瘤和无症状携带者的白血病相关信号通路。

IF 1.5 4区 医学 Q4 IMMUNOLOGY AIDS research and human retroviruses Pub Date : 2024-08-08 DOI:10.1089/AID.2024.0010
Saber Soltani, Sayed-Hamidreza Mozhgani, Roozbeh Roohinezhad, Setareh Hedayati Emami, Mah Hedayati Emami, Setayesh Solooki, Mina Fattah Hesari, Niloofar Doroozeh, Mehdi Norouzi
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引用次数: 0

摘要

背景和目的:人类 T 细胞淋巴细胞病毒 1 型(HTLV-1)与成人 T 细胞白血病/淋巴瘤(ATLL)(一种胎儿恶性感染)有关。最近,HTLV-1 新型无症状病人(ACs)在献血者中频频出现。了解与 HTLV-1 相关的分子发病机制的深刻概念有助于找到新的治疗策略。本研究旨在确定 ATLL 中与白血病相关的信号调控:将 30 名参与者分为三组进行评估,包括 10 名 ATLL 患者、10 名 ACs 和 10 名正常对照组。从 ATLL 患者中分离出无化疗史的血液样本。此外,还从 ACs 和正常人身上采集了血液样本。对采集的血液样本进行淋巴细胞分离。然后,从制备好的样本中提取 RNA 并用于 cDNA 合成。利用实时 PCR 技术研究了作为病毒基因的 Tax 和 HBZ 以及细胞基因,包括 MKP-1、EVI-1、JNK-1、FOXO-1、AKT-1、DEPTOR、MTOR 和 JUN:ALL患者的平均年龄为(53.2±7.32)岁,其中9人(90%)为男性。与内部对照相比,EVI-1 和 FOXO-1 的表达水平与 ATLL 患者有显著相关性。结论:发现病毒和细胞调控机制是治疗ALL的关键:结论:发现调控 HTLV-1 转化的病毒和细胞信号通路至关重要。结论:发现调控 HTLV-1 转化的病毒和细胞信号通路至关重要,可以考虑采用新的治疗策略在体内调控 ATLL 的细胞信号通路。因此,建议使用相关细胞信号通路的激活剂和抑制剂对 ATLL 进行细胞治疗的临床试验。建议对 FOXO-1 和 EVI-1 进行更多研究,以这些基因为靶点揭示 ATLL 的分子发病机制。
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Leukemia-Related Signaling Pathways Among HTLV-1-Derived Adult T Cell Leukemia/Lymphoma and Asymptomatic Carriers in Comparison to Normal Group.

Human T cell lymphotropic virus type 1 (HTLV-1) is associated with adult T cell leukemia/lymphoma (ATLL), a fetal malignant infection. Recently, HTLV-1 new asymptomatic carriers (ACs) have frequently been reported among blood donors. Reaching the profound concept of HTLV-1-associated molecular pathogenesis could result in finding novel therapeutic strategies. The current study aimed to determine leukemia-related signaling regulation in ATLL. Thirty participants were evaluated in 3 groups, including 10 ATLL patients, 10 ACs, and 10 normal controls. Blood samples were isolated without any chemotherapy history from ATLL patients. Also, blood samples were recovered from ACs and normal individuals. White blood cells isolation was done on the collected blood samples. After this, RNA was extracted from the prepared samples and used for the cDNA synthesis. TAX and HTLV-1 basic leucine zipper factor as viral genes and cellular genes, including MKP-1, EVI-1, JNK-1, FOXO-1, AKT-1, DEPTOR, MTOR, and JUN, were investigated using real-time PCR. The mean age of ATLL patients was 53.2 ± 7.32 years, and 9 (90%) were male. The EVI-1 and FOXO-1 expression levels were significantly associated with ATLL patients compared with the internal control. However, the significant differences in expression of other genes in the remaining groups were not seen. Discovering viral and cellular signaling pathways that regulate HTLV-1 transformation is essential. A novel therapeutic strategy for ATLL-regulating cellular signaling pathways in vivo could be considered. Therefore, clinical trials using activators and inhibitors of related cellular signaling pathways for cell therapy of ATLL are recommended. It is recommended that more investigation be conducted on FOXO-1 and EVI-1 to target these genes and reveal the molecular pathogenesis of ATLL.

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来源期刊
CiteScore
3.10
自引率
6.70%
发文量
201
审稿时长
3-6 weeks
期刊介绍: AIDS Research and Human Retroviruses was the very first AIDS publication in the field over 30 years ago, and today it is still the critical resource advancing research in retroviruses, including AIDS. The Journal provides the broadest coverage from molecular biology to clinical studies and outcomes research, focusing on developments in prevention science, novel therapeutics, and immune-restorative approaches. Cutting-edge papers on the latest progress and research advances through clinical trials and examination of targeted antiretroviral agents lead to improvements in translational medicine for optimal treatment outcomes. AIDS Research and Human Retroviruses coverage includes: HIV cure research HIV prevention science - Vaccine research - Systemic and Topical PreP Molecular and cell biology of HIV and SIV Developments in HIV pathogenesis and comorbidities Molecular biology, immunology, and epidemiology of HTLV Pharmacology of HIV therapy Social and behavioral science Rapid publication of emerging sequence information.
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