Upregulation of SNHG7 and FAIM2 Expression Levels in Chronic Myelogenous Leukemia Patients Compared with Normal Subjects

Abstract

Background: Chronic myelogenous leukemia (CML), also known as chronic granulocytic leukemia (CGL), is considered a hematological malignancy with a prevalence of 1.9 per 100,000 population. Recent studies have shown the role of SNHGs in proliferation, apoptosis, CML progression, and even drug resistance through interaction with miRNAs. The positive correlation between lncRNA-small nucleus RNA host gene 7 (SNHG7) and Fas apoptosis inhibitory molecule 2 (FAIM2) with different cancers has been proved. Objectives: This study investigated the role of SNHG7 and FAIM2 in CML for the first time and revealed the potential correlation between these genes. Methods: This examine changed was performed with a case-manipulate design. First, the accuracy of persistent myeloid leukemia changed with the aid of using karyotype in addition to molecular and cell methods. After RNA extraction from white blood cells and cDNA synthesis, gene expression changed into measured with the use of real-time PCR. Finally, the facts have been statistically analyzed. Results: The results of this study showed that the expression levels of SNHG7 and FAIM2 were significantly increased in chronic myelogenous leukemia patients compared with normal individuals (P-value < 0.001). This increased expression may indicate a potential role for this molecule in the progression and development of this cancer. Conclusions: The current study demonstrates the effective roles of SNHG7 and FAIM2 in the progression of chronic myeloid leukemia, which can be investigated in future studies as biomarkers and potential therapeutic targets.