tRNA-derived fragments as novel potential biomarkers for relapsed/refractory multiple myeloma

Abstract Background tRNA-derived fragments have been reported to be key regulatory factors in human tumors. However, their roles in the progression of multiple myeloma remain unknown. Results This study employed RNA-sequencing to explore the expression profiles of tRFs/tiRNAs in new diagnosed MM and...

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Main Authors: Cong Xu, Ting Liang, Fangrong Zhang, Jing Liu, Yunfeng Fu
Format: Article
Language:English
Published: BMC 2021-05-01
Series:BMC Bioinformatics
Subjects:
Online Access:https://doi.org/10.1186/s12859-021-04167-8
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spelling doaj-97e6bce73a1a4a53baae8d6d6689b0ca2021-05-11T15:01:31ZengBMCBMC Bioinformatics1471-21052021-05-0122111210.1186/s12859-021-04167-8tRNA-derived fragments as novel potential biomarkers for relapsed/refractory multiple myelomaCong Xu0Ting Liang1Fangrong Zhang2Jing Liu3Yunfeng Fu4Department of Hematology, The Third Xiangya Hospital of Central South UniversityDepartment of Blood Transfusion, The Seventh Affiliated Hospital of Sun Yat-Sen UniversityDepartment of Hematology, The Third Xiangya Hospital of Central South UniversityDepartment of Hematology, The Third Xiangya Hospital of Central South UniversityDepartment of Blood Transfusion, The Third Xiangya Hospital of Central South UniversityAbstract Background tRNA-derived fragments have been reported to be key regulatory factors in human tumors. However, their roles in the progression of multiple myeloma remain unknown. Results This study employed RNA-sequencing to explore the expression profiles of tRFs/tiRNAs in new diagnosed MM and relapsed/refractory MM samples. The expression of selected tRFs/tiRNAs were further validated in clinical specimens and myeloma cell lines by qPCR. Bioinformatic analysis was performed to predict their roles in multiple myeloma progression.We identified 10 upregulated tRFs/tiRNAs and 16 downregulated tRFs/tiRNAs. GO enrichment and KEGG pathway analysis were performed to analyse the functions of 1 significantly up-regulated and 1 significantly down-regulated tRNA-derived fragments. tRFs/tiRNAs may be involved in MM progression and drug-resistance. Conclusion tRFs/tiRNAs were dysregulated and could be potential biomarkers for relapsed/refractory MM.https://doi.org/10.1186/s12859-021-04167-8Multiple myelomaTRNA related fragmentsTRNA halvesRelapsed/refractoryBiomarkers
collection DOAJ
language English
format Article
sources DOAJ
author Cong Xu
Ting Liang
Fangrong Zhang
Jing Liu
Yunfeng Fu
spellingShingle Cong Xu
Ting Liang
Fangrong Zhang
Jing Liu
Yunfeng Fu
tRNA-derived fragments as novel potential biomarkers for relapsed/refractory multiple myeloma
BMC Bioinformatics
Multiple myeloma
TRNA related fragments
TRNA halves
Relapsed/refractory
Biomarkers
author_facet Cong Xu
Ting Liang
Fangrong Zhang
Jing Liu
Yunfeng Fu
author_sort Cong Xu
title tRNA-derived fragments as novel potential biomarkers for relapsed/refractory multiple myeloma
title_short tRNA-derived fragments as novel potential biomarkers for relapsed/refractory multiple myeloma
title_full tRNA-derived fragments as novel potential biomarkers for relapsed/refractory multiple myeloma
title_fullStr tRNA-derived fragments as novel potential biomarkers for relapsed/refractory multiple myeloma
title_full_unstemmed tRNA-derived fragments as novel potential biomarkers for relapsed/refractory multiple myeloma
title_sort trna-derived fragments as novel potential biomarkers for relapsed/refractory multiple myeloma
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2021-05-01
description Abstract Background tRNA-derived fragments have been reported to be key regulatory factors in human tumors. However, their roles in the progression of multiple myeloma remain unknown. Results This study employed RNA-sequencing to explore the expression profiles of tRFs/tiRNAs in new diagnosed MM and relapsed/refractory MM samples. The expression of selected tRFs/tiRNAs were further validated in clinical specimens and myeloma cell lines by qPCR. Bioinformatic analysis was performed to predict their roles in multiple myeloma progression.We identified 10 upregulated tRFs/tiRNAs and 16 downregulated tRFs/tiRNAs. GO enrichment and KEGG pathway analysis were performed to analyse the functions of 1 significantly up-regulated and 1 significantly down-regulated tRNA-derived fragments. tRFs/tiRNAs may be involved in MM progression and drug-resistance. Conclusion tRFs/tiRNAs were dysregulated and could be potential biomarkers for relapsed/refractory MM.
topic Multiple myeloma
TRNA related fragments
TRNA halves
Relapsed/refractory
Biomarkers
url https://doi.org/10.1186/s12859-021-04167-8
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