Inhibition of protein translational machinery in triple-negative breast cancer as a promising therapeutic strategy.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 38729158.
- Also identified by DOI 10.1016/j.xcrm.2024.101552 and PMC identifier 11148772.
- 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
Y-box binding protein-1 (YB-1) is a proto-oncogenic protein associated with protein translation regulation. It plays a crucial role in the development and progression of triple-negative breast cancer (TNBC). In this study, we describe a promising approach to inhibit YB-1 using SU056, a small-molecule inhibitor. SU056 physically interacts with YB-1 and reduces its expression, which helps to restrain the progression of TNBC. Proteome profiling analysis indicates that the inhibition of YB-1 by SU056 can alter the proteins that regulate protein translation, an essential process for cancer cell growth. Preclinical studies on human cells, mice, and patient-derived xenograft tumor models show the effectiveness of SU056. Moreover, toxicological studies have shown that SU056 treatment and dosing are well tolerated without any adverse effects. Overall, our study provides a strong foundation for the further development of SU056 as a potential treatment option for patients with TNBC by targeting YB-1.
Medical subject headings
- Triple Negative Breast Neoplasms
- Y-Box-Binding Protein 1
- Protein Biosynthesis
- Xenograft Model Antitumor Assays