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tRNA-Derived Fragments as Novel Predictive Biomarkers for Trastuzumab-Resistant Breast Cancer.

Authors :
Sun, Chunxiao
Yang, Fan
Zhang, Yanhong
Chu, Jiahui
Wang, Jian
Wang, Yifan
Zhang, Yanqiu
Li, Jun
Li, Yongfei
Fan, Ruihua
Li, Wei
Huang, Xiang
Wu, Hao
Fu, Ziyi
Jiang, Zefei
Yin, Yongmei
Source :
Cellular Physiology & Biochemistry (Karger AG). Sep2018, Vol. 49 Issue 2, p419-431. 13p.
Publication Year :
2018

Abstract

<bold>Background/Aims:</bold> Resistance to trastuzumab remains a common challenge to HER-2 positive breast cancer. Up until now, the underlying mechanism of trastuzumab resistance is still unclear. tRNA-derived small non-coding RNAs, a new class of small non-coding RNA (sncRNAs), have been observed to play an important role in cancer progression. However, the relationship between tRNA-derived fragments and trastuzumab resistance is still unknown. <bold>Methods:</bold> We detected the levels of tRNA-derived fragments expression in normal breast epithelial cell lines, trastuzumab-sensitive and -resistant breast cancer cell lines using high-throughput sequencing. qRT-PCR was conducted to validate the differentially expressed fragments in serums from trastuzumab-sensitive and -resistant patients. A receiver operating characteristic (ROC) curve analysis was performed to evaluate the power of specific tRNA-derived fragments. Progression-free survival (PFS) was analyzed using Cox-regression. <bold>Results:</bold> Our sequence results showed that tRNA-derived fragments were differentially expressed in the HBL-100, SKBR3, and JIMT-1 cell lines. tRF-30-JZOYJE22RR33 and tRF-27-ZDXPHO53KSN were found significantly upregulated in trastuzumab-resistant patients compared to sensitive individuals, and the ROC analysis showed that tRF-30-JZOYJE22RR33 and tRF-27-ZDXPHO53KSN were correlated with trastuzumab resistance. In a multivariate analysis, higher levels of tRF-30-JZOYJE22RR33 and tRF-27-ZDXPHO53KSN expression were associated with significantly shorter PFS in patients with metastatic HER-2 positive breast cancer. <bold>Conclusion:</bold> Our results suggest that tRF-30-JZOYJE22RR33 and tRF-27-ZDXPHO53KSN play important roles in trastuzumab resistance. Patients with high levels of tRF-30-JZOYJE22RR33 and tRF-27-ZDXPHO53KSN expression benefitted less from trastuzumab-based therapy than those that express lower-levels of these molecules. tRF-30-JZOYJE22RR33 and tRF-27-ZDXPHO53KSN may be potential biomarkers and intervention targets in the clinical treatment of trastuzumab-resistant breast cancer. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10158987
Volume :
49
Issue :
2
Database :
Academic Search Index
Journal :
Cellular Physiology & Biochemistry (Karger AG)
Publication Type :
Academic Journal
Accession number :
131635405
Full Text :
https://doi.org/10.1159/000492977