Department of Cancer Genetics, Istanbul Faculty of Medicine, Oncology Institute, Istanbul University, Istanbul, Turkey.
Health Services Vocational School of Higher Education, T.C. Istanbul Aydin University, Istanbul, Turkey.
Pathol Oncol Res. 2022 Jan 24;28:1610055. doi: 10.3389/pore.2022.1610055. eCollection 2022.
MicroRNAs (miRNAs) are the non-coding RNAs that can both attach to the untranslated and coding sections of target mRNAs, triggering destruction or post-transcriptional alteration. miRNAs regulate various cellular processes such as immune function, apoptosis, and tumorigenesis. About 35,000 miRNAs have been discovered in the human genome. The increasing evidence suggests that the dysregulation of human miRNAs may have a role in the etiology of some disorders including cancer. Only a small sub-set of human miRNAs has functionally been validated in the pathogenesis of oncogenic viruses such as Kaposi's sarcoma-associated herpesvirus (KSHV). KSHV is the cause of various human malignancies including primary effusion lymphoma (PEL) and Kaposi's sarcoma (KS), which are mainly seen in AIDS patients or other immunocompromised people. We aimed to identify the miRNAs in Kaposi's sarcoma cases, with the comparison of KSHV seropositive and seronegative tumors with the controls and in each other in Turkish Kaposi's sarcoma patients. We performed the miRNA-sequencing at genome level in the peripheral blood mononuclear cells of 16 Kaposi's sarcoma patients, and in 8 healthy controls matched for age, gender, and ethnicity. A total of 642 miRNA molecules with different expression profiles were identified between the patients and the healthy controls. Currently, out of 642 miRNAs, 7 miRNAs (miR-92b-3p, miR-490-3p, miR-615-3p, miR-629-5p, miR-1908, miR-3180, miR-4433b-3p) which have not been described in the literature in the context of Kaposi's sarcoma were addressed in the study for the first time and 9 novel miRNAs, not found previously in the database, have been detected in Kaposi's sarcoma using the miRNA-sequencing technique. This study demonstrates the identification of differently expressed miRNAs which might be the new therapeutic targets for Kaposi's sarcoma, that has limited treatment options and can be used in the etiology, diagnosis, and prognosis of this cancer.
微小 RNA(miRNA)是一种非编码 RNA,可以与靶 mRNA 的非翻译和编码区结合,从而触发破坏或转录后改变。miRNA 调节各种细胞过程,如免疫功能、细胞凋亡和肿瘤发生。人类基因组中已发现约 35000 种 miRNA。越来越多的证据表明,人类 miRNA 的失调可能在某些疾病的发病机制中起作用,包括癌症。只有一小部分人类 miRNA 在致癌病毒(如卡波济肉瘤相关疱疹病毒(KSHV))的发病机制中得到了功能验证。KSHV 是包括原发性渗出性淋巴瘤(PEL)和卡波济肉瘤(KS)在内的多种人类恶性肿瘤的病因,主要见于艾滋病患者或其他免疫功能低下的人群。我们旨在鉴定卡波济肉瘤病例中的 miRNA,并将 KSHV 血清阳性和血清阴性肿瘤与对照组以及土耳其卡波济肉瘤患者之间进行比较。我们对 16 例卡波济肉瘤患者和 8 例年龄、性别和种族匹配的健康对照者的外周血单核细胞进行了全基因组 miRNA 测序。在患者和健康对照者之间鉴定出 642 种具有不同表达谱的 miRNA 分子。目前,在 642 种 miRNA 中,有 7 种 miRNA(miR-92b-3p、miR-490-3p、miR-615-3p、miR-629-5p、miR-1908、miR-3180、miR-4433b-3p)在卡波济肉瘤的文献中尚未描述,在研究中首次提出,使用 miRNA 测序技术在卡波济肉瘤中检测到 9 种新的 miRNA,这些 miRNA 以前在数据库中没有发现。本研究表明,鉴定出差异表达的 miRNA 可能是卡波济肉瘤的新治疗靶点,卡波济肉瘤的治疗选择有限,可用于该癌症的病因学、诊断和预后。