Abstract
HER2 upregulation is related with poor outcome in many tumor types. Whereas anti-HER2 treatment is the standard approach as adjuvant therapy in HER2-overexpressing breast cancer, the frequent relapses reinforce the need for alternative treatments. Here we used next-generation sequencing (NGS) to evaluate miRNAs and circRNAs in the cell-lines HB4a and C5.2, where the latter is a HER2-overexpressing clone of the former, and also from two different populations of their secreted extracellular vesicles. Whereas circRNA-levels were stable, we found at least 16 miRNAs apparently modulated by HER2-expression. The miR223-3p, miR-421 and miR-21-5p were validated in an independent cohort of 431 breast cancer patients from The Cancer Genome Atlas (TCGA). The consistent modulation of these molecules and their possible involvement in the HER2-axis makes them promising new targets to overcome HER2-activation.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 493-502 |
| Number of pages | 10 |
| Journal | Pharmacogenomics |
| Volume | 20 |
| Issue number | 7 |
| DOIs | |
| State | Published - May 24 2019 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2019 Future Medicine Ltd.
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