A serum microRNA signature predicts trastuzumab benefit in HER2-positive metastatic breast cancer patients.
other · Level V
Where this comes from
- Record sourced from PubMed, PMID 29691399.
- Also identified by DOI 10.1038/s41467-018-03537-w and PMC identifier 5915573.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Trastuzumab is a standard treatment for HER2-positive (HER2<sup>+</sup>) breast cancer, but some patients are refractory to the therapy. MicroRNAs (miRNAs) have been used to predict therapeutic effects for various cancers, but whether miRNAs can serve as biomarkers for HER2<sup>+</sup> metastatic breast cancer (MBC) patients remains unclear. Using miRNA microarray, we identify 13 differentially expressed miRNAs in the serum of HER2<sup>+</sup> MBC patients with distinct response to trastuzumab, and four miRNAs are selected to construct a signature to predict survival using LASSO model. Further, our data show that miR-940 is mainly released from the tumor cells and miR-451a, miR-16-5p and miR-17-3p are mainly from the immune cells. All these four miRNAs directly target signaling molecules that play crucial roles in regulating trastuzumab resistance. In summary, we develop a serum-based miRNA signature that potentially predicts the therapeutic benefit of trastuzumab for HER2<sup>+</sup> MBC patients and warrants future validation in prospective clinical trials.
Medical subject headings
- Antineoplastic Agents
- Breast Neoplasms
- MicroRNAs
- Erb-b2 Receptor Tyrosine Kinases
- Trastuzumab