Identification of tRNA-Derived Fragments Expression Profile in Breast Cancer Tissues. Article

Wang, Xiaoming, Yang, Yining, Tan, Xuyan et al. (2019). Identification of tRNA-Derived Fragments Expression Profile in Breast Cancer Tissues. . Current Genomics, 20(3), 199-213. 10.2174/1389202920666190326145459

cited authors

  • Wang, Xiaoming; Yang, Yining; Tan, Xuyan; Mao, Xuelian; Wei, Da; Yao, Yufeng; Jiang, Pan; Mo, Dongping; Wang, Ting; Yan, Feng

authors

abstract

  • BACKGROUND:: In recent years, tRFs(transfer RNA-Derived Fragments) and transfer RNADerived Stress-induced RNAs (or tRNA halves) have been shown to have vital roles in cancer biology.We aimed to reveal the expression profile of tRNA-derived fragments in breast cancer tissues in the study, and to explore their potential as biomarkers of breast cancer. METHODS:: We characterized the tRNA-derived fragments expression profile from 6 paired clinical breast cancer tissues and adjacent normal samples. Then we selected 6 significantly expressed tRNAderived fragments and screened the genes for validation by using Quantitative Real-time PCR. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes biological pathway were finally analyzed. RESULTS:: We found 30 differentially expressed tRNA-derived fragments across our dataset, out of which 17 were up-regulated, and 13 were down-regulated. Compared with 16 clinical breast cancer tissues and adjacent normal tissues by qPCR, the results demonstrated that tRF-32-Q99P9P9NH57SJ(FC = -2.6476, p = 0.0189), tRF-17-79MP9PP (FC = -4.8984, p = 0.0276) and tRF-32-XSXMSL73VL4YK (FC = 6.5781, p = 0.0226) were significantly expressed in breast cancer tissues(p < 0.001). tRF-32-XSXMSL73VL4YK was significantly up-regulated, and tRF-32-Q99P9P9NH57SJ and tRF-17-79MP9PP were significantly down-regulated in which the expressionpatterns were similar to the sequencing results. The top ten significant results of GO and KEGG pathways enrichment analysis were presented. CONCLUSION:: Our studies have demonstrated that there were significantly expressed tRNA-derived fragments in breast cancer tissues. They are hopefully to become biomarkers and would be valuable researches in this area.

publication date

  • April 1, 2019

published in

keywords

  • Biomarker
  • Breast cancer
  • Expression profile
  • Gene ontology
  • Genomes
  • TRNA-derived fragments

Location

  • United Arab Emirates

Digital Object Identifier (DOI)

start page

  • 199

end page

  • 213

volume

  • 20

issue

  • 3