Sajjadi-Dokht Mehdi, Merza Mohamad Talar Ahmad, Sulaiman Rahman Heshu, Suliman Maashi Marwah, Danshina Svetlana, Shomali Navid, Solali Saeed, Marofi Faroogh, Zeinalzadeh Elham, Akbari Morteza, Adili Ali, Aslaminabad Ramin, Farshdousti Hagh Majid, Jarahian Mostafa
Immunology Research Center, Tabriz University of Medical Sciences, Tabriz 5166614766, Iran.
Department of Pharmacology, College of Pharmacy, Hawler Medical University, Erbil 44001, Iraq.
Genes Dis. 2021 Dec 3;9(4):849-867. doi: 10.1016/j.gendis.2021.10.009. eCollection 2022 Jul.
Blood disorders include a wide spectrum of blood-associated malignancies resulting from inherited or acquired defects. The ineffectiveness of existing therapies against blood disorders arises from different reasons, one of which is drug resistance, so different types of leukemia may show different responses to treatment. Leukemia occurs for a variety of genetic and acquired reasons, leading to uncontrolled proliferation in one or more cell lines. Regarding the genetic defects, oncogene signal transducer and activator of transcription (STAT) family transcription factor, especially STAT3, play an essential role in hematological disorders onset and progress upon mutations, dysfunction, or hyperactivity. Besides, microRNAs, as biological molecules, has been shown to play a dual role in either tumorigenesis and tumor suppression in various cancers. Besides, a strong association between STAT3 and miRNA has been reported. For example, miRNAs can regulate STAT3 via targeting its upstream mediators such as IL6, IL9, and JAKs or directly binding to the gene. On the other hand, STAT3 can regulate miRNAs. In this review study, we aimed to determine the role of either microRNAs and STAT3 along with their effect on one another's activity and function in hematological malignancies.
血液疾病包括由遗传或后天缺陷引起的一系列与血液相关的恶性肿瘤。现有治疗血液疾病的方法无效有多种原因,其中之一是耐药性,因此不同类型的白血病对治疗可能表现出不同的反应。白血病的发生有多种遗传和后天原因,导致一种或多种细胞系不受控制地增殖。关于遗传缺陷,致癌基因信号转导和转录激活因子(STAT)家族转录因子,尤其是STAT3,在血液系统疾病的发生和进展中,在发生突变、功能障碍或活性过高时发挥着重要作用。此外,微小RNA作为生物分子,已被证明在各种癌症的肿瘤发生和肿瘤抑制中起双重作用。此外,有报道称STAT3与微小RNA之间存在密切关联。例如,微小RNA可通过靶向其上游介质如IL6、IL9和JAKs或直接与基因结合来调节STAT3。另一方面,STAT3可以调节微小RNA。在本综述研究中,我们旨在确定微小RNA和STAT3在血液系统恶性肿瘤中的作用,以及它们对彼此活性和功能的影响。