Background:
Acquired immune deficiency syndrome-related lymphoma (ARL) is closely related to Epstein-Barr virus (EBV) infection. However, there are few studies on the occurrence and development of EBV microRNAs (miRNAs) in ARL patients.
Methods:
The plasma of 5 EBV-infected ARL patients and 8 EBV-infected HIV patients were screened for EBV miRNAs differentially expressed between the two groups through a customized EBV microRNA quantification chip. The plasma of 35 EBV-infected ARL patients and 20 EBV-infected HIV patients was verified by qRT-PCR expanded samples. And we gave a further analysis of the correlation between differentially expressed EBV miRNAs and clinical indicators in ARL patients.
Results:
1. There were differential expressions of EBV miRNAs in the plasma of EBV-infected ARL patients and EBV-infected HIV patients. It was found that ebv-miR-BART2-5p, ebv-miR-BART8-3p, ebv-miR-BART15, ebv-miR-BART19-5p expression was significantly up-regulated and ebv-miR-BART9-5p expression was significantly down-regulated; 2. EBV miRNAs with significantly different expressions in the screening results were expanded and verified by qRT-PCR, and the differential expression was found to be consistent with the screening results; 3. The relative expression levels of ebv-miR-BART8-3p,ebv-miR-BART19-5p and ebv-miR-BART9-5p in plasma were positive correlated with the international prognostic index (IPI) score of Lymphoma, eastern cooperative oncology group (ECOG) scores are the incidence of lymphoma B symptoms (P = 0.03, 0.01, and 0.04, respectively);4. EBV miRNAs could be used as biomarkers for ARL prognosis evaluation.
Conclusions:
The expression of ebv-miR-BART2-5p, ebv-miR-BART8-3p, ebv-miR-BART15, ebv-miR-BART19-5p, ebv-miR-BART9-5p and ebv-miR-BART6-3p in ARL patients were highly different; and ebv-miR-BART8-3p, ebv-miR-BART19-5p, ebv-miR-BART9-5p could be used as the biomarkers of the prognosis of ARL evaluation.
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No competing interests reported.
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Posted 03 Mar, 2021
Posted 03 Mar, 2021
Background:
Acquired immune deficiency syndrome-related lymphoma (ARL) is closely related to Epstein-Barr virus (EBV) infection. However, there are few studies on the occurrence and development of EBV microRNAs (miRNAs) in ARL patients.
Methods:
The plasma of 5 EBV-infected ARL patients and 8 EBV-infected HIV patients were screened for EBV miRNAs differentially expressed between the two groups through a customized EBV microRNA quantification chip. The plasma of 35 EBV-infected ARL patients and 20 EBV-infected HIV patients was verified by qRT-PCR expanded samples. And we gave a further analysis of the correlation between differentially expressed EBV miRNAs and clinical indicators in ARL patients.
Results:
1. There were differential expressions of EBV miRNAs in the plasma of EBV-infected ARL patients and EBV-infected HIV patients. It was found that ebv-miR-BART2-5p, ebv-miR-BART8-3p, ebv-miR-BART15, ebv-miR-BART19-5p expression was significantly up-regulated and ebv-miR-BART9-5p expression was significantly down-regulated; 2. EBV miRNAs with significantly different expressions in the screening results were expanded and verified by qRT-PCR, and the differential expression was found to be consistent with the screening results; 3. The relative expression levels of ebv-miR-BART8-3p,ebv-miR-BART19-5p and ebv-miR-BART9-5p in plasma were positive correlated with the international prognostic index (IPI) score of Lymphoma, eastern cooperative oncology group (ECOG) scores are the incidence of lymphoma B symptoms (P = 0.03, 0.01, and 0.04, respectively);4. EBV miRNAs could be used as biomarkers for ARL prognosis evaluation.
Conclusions:
The expression of ebv-miR-BART2-5p, ebv-miR-BART8-3p, ebv-miR-BART15, ebv-miR-BART19-5p, ebv-miR-BART9-5p and ebv-miR-BART6-3p in ARL patients were highly different; and ebv-miR-BART8-3p, ebv-miR-BART19-5p, ebv-miR-BART9-5p could be used as the biomarkers of the prognosis of ARL evaluation.
Figure 1
Figure 2
Figure 3
Figure 4
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