Modulation of Cellular MicroRNA by HIV-1 in Burkitt Lymphoma Cells—A Pathway to Promoting Oncogenesis

Viruses and viral components have been shown to manipulate the expression of host microRNAs (miRNAs) to their advantage, and in some cases to play essential roles in cancer pathogenesis. Burkitt lymphoma (BL), a highly aggressive B-cell derived cancer, is significantly over-represented among people...

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Main Authors: Beatrice Relebogile Ramorola, Taahira Goolam-Hoosen, Leonardo Alves de Souza Rios, Shaheen Mowla
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Genes
Subjects:
Online Access:https://www.mdpi.com/2073-4425/12/9/1302
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author Beatrice Relebogile Ramorola
Taahira Goolam-Hoosen
Leonardo Alves de Souza Rios
Shaheen Mowla
author_facet Beatrice Relebogile Ramorola
Taahira Goolam-Hoosen
Leonardo Alves de Souza Rios
Shaheen Mowla
author_sort Beatrice Relebogile Ramorola
collection DOAJ
description Viruses and viral components have been shown to manipulate the expression of host microRNAs (miRNAs) to their advantage, and in some cases to play essential roles in cancer pathogenesis. Burkitt lymphoma (BL), a highly aggressive B-cell derived cancer, is significantly over-represented among people infected with HIV. This study adds to accumulating evidence demonstrating that the virus plays a direct role in promoting oncogenesis. A custom miRNA PCR was used to identify 32 miRNAs that were differently expressed in Burkitt lymphoma cells exposed to HIV-1, with a majority of these being associated with oncogenic processes. Of those, hsa-miR-200c-3p, a miRNA that plays a crucial role in cancer cell migration, was found to be significantly downregulated in both the array and in single-tube validation assays. Using an in vitro transwell system we found that this downregulation correlated with significantly enhanced migration of BL cells exposed to HIV-1. Furthermore, the expression of the ZEB1 and ZEB2 transcription factors, which are promotors of tumour invasion and metastasis, and which are direct targets of hsa-miR-200c-3p, were found to be enhanced in these cells. This study therefore identifies novel miRNAs as role players in the development of HIV-associated BL, with one of these miRNAs, hsa-miR-200c-3p, being a candidate for further clinical studies as a potential biomarker for prognosis in patients with Burkitt lymphoma, who are HIV positive.
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spelling doaj.art-2af4b44604c64b32ac0f5fd2399479612023-11-22T13:12:55ZengMDPI AGGenes2073-44252021-08-01129130210.3390/genes12091302Modulation of Cellular MicroRNA by HIV-1 in Burkitt Lymphoma Cells—A Pathway to Promoting OncogenesisBeatrice Relebogile Ramorola0Taahira Goolam-Hoosen1Leonardo Alves de Souza Rios2Shaheen Mowla3Division of Haematology, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Observatory 7925, Cape Town 7700, South AfricaDivision of Haematology, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Observatory 7925, Cape Town 7700, South AfricaDivision of Haematology, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Observatory 7925, Cape Town 7700, South AfricaDivision of Haematology, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Observatory 7925, Cape Town 7700, South AfricaViruses and viral components have been shown to manipulate the expression of host microRNAs (miRNAs) to their advantage, and in some cases to play essential roles in cancer pathogenesis. Burkitt lymphoma (BL), a highly aggressive B-cell derived cancer, is significantly over-represented among people infected with HIV. This study adds to accumulating evidence demonstrating that the virus plays a direct role in promoting oncogenesis. A custom miRNA PCR was used to identify 32 miRNAs that were differently expressed in Burkitt lymphoma cells exposed to HIV-1, with a majority of these being associated with oncogenic processes. Of those, hsa-miR-200c-3p, a miRNA that plays a crucial role in cancer cell migration, was found to be significantly downregulated in both the array and in single-tube validation assays. Using an in vitro transwell system we found that this downregulation correlated with significantly enhanced migration of BL cells exposed to HIV-1. Furthermore, the expression of the ZEB1 and ZEB2 transcription factors, which are promotors of tumour invasion and metastasis, and which are direct targets of hsa-miR-200c-3p, were found to be enhanced in these cells. This study therefore identifies novel miRNAs as role players in the development of HIV-associated BL, with one of these miRNAs, hsa-miR-200c-3p, being a candidate for further clinical studies as a potential biomarker for prognosis in patients with Burkitt lymphoma, who are HIV positive.https://www.mdpi.com/2073-4425/12/9/1302MicroRNAmiR-200cBurkitt lymphomaHIV-1non-Hodgkin lymphomaZEB
spellingShingle Beatrice Relebogile Ramorola
Taahira Goolam-Hoosen
Leonardo Alves de Souza Rios
Shaheen Mowla
Modulation of Cellular MicroRNA by HIV-1 in Burkitt Lymphoma Cells—A Pathway to Promoting Oncogenesis
Genes
MicroRNA
miR-200c
Burkitt lymphoma
HIV-1
non-Hodgkin lymphoma
ZEB
title Modulation of Cellular MicroRNA by HIV-1 in Burkitt Lymphoma Cells—A Pathway to Promoting Oncogenesis
title_full Modulation of Cellular MicroRNA by HIV-1 in Burkitt Lymphoma Cells—A Pathway to Promoting Oncogenesis
title_fullStr Modulation of Cellular MicroRNA by HIV-1 in Burkitt Lymphoma Cells—A Pathway to Promoting Oncogenesis
title_full_unstemmed Modulation of Cellular MicroRNA by HIV-1 in Burkitt Lymphoma Cells—A Pathway to Promoting Oncogenesis
title_short Modulation of Cellular MicroRNA by HIV-1 in Burkitt Lymphoma Cells—A Pathway to Promoting Oncogenesis
title_sort modulation of cellular microrna by hiv 1 in burkitt lymphoma cells a pathway to promoting oncogenesis
topic MicroRNA
miR-200c
Burkitt lymphoma
HIV-1
non-Hodgkin lymphoma
ZEB
url https://www.mdpi.com/2073-4425/12/9/1302
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