MicroRNA Expression Profiling of Diffuse Large B-Cell Lymphoma

• Published in: Molecular biology (New York) Vol. 57; no. 3; pp. 475 - 481
• Main Authors: Veryaskina, Yu. A., Titov, S. E., Kovynev, I. B., Fyodorova, S. S., Shebunyaeva, Ya. Yu, Antonenko, O. V., Pospelova, T. I., Zhimulev, I. F.
• Format: Journal Article
• Language: English
• Published: Moscow Pleiades Publishing 01.06.2023; Springer Nature B.V
• Subjects: B-cell lymphoma; Biochemistry; Bioinformatics; Biomedical and Life Sciences; Biopsy; Chemotherapy; Genomics. Transcriptomics; Hemopoiesis; Human Genetics; Life Sciences; Lymph nodes; Lymphadenopathy; Lymphatic system; Lymphocytes B; Lymphoma; Lymphopoiesis; MicroRNAs; miRNA; Non-Hodgkin's lymphoma; Patients; Radiation therapy; Remission; Therapeutic targets; microRNA; hematopoiesis; non-Hodgkin lymphoma; diffuse large B-cell lymphoma; lymphoma
• ISSN: 0026-8933; 1608-3245
• DOI: 10.1134/S0026893323030159

Non-Hodgkin lymphoma (NHL) is a heterogeneous group of cancers that differ in pathogenesis and prognosis. The main methods of treating NHL include chemotherapy, immunochemotherapy, and radiation therapy. However, a significant proportion of these tumors are chemoresistant or rapidly recur after a short chemotherapy-induced remission. In this regard, the search for alternative cytoreductive therapeutic methods is relevant. Aberrant expression of microRNA (miRNA) is one of the mechanisms responsible for the emergence and progression of malignant lymphoid neoplasms. We analyzed the profile of miRNA expression in the biopsy material from lymph nodes affected by diffuse large B-cell lymphoma (DLBCL). The key material of the study was histological preparations of lymph nodes obtained by excisional diagnostic biopsy and treated using conventional histomorphological formalin fixation methods. The study group consisted of patients with DLBCL ( n = 52); the control group consisted of patients with reactive lymphadenopathy (RL) ( n = 40). It was shown that the miR-150 expression level in DLBCL was reduced by more than 12 times ( p = 3.6 × 10 ‒15 ) compared with RL. Bioinformatics analysis revealed the involvement of miR-150 in the regulation of hematopoiesis and lymphopoiesis. The data we obtained allow us to consider miR-150 as a promising therapeutic target with great potential in clinical practice.