Aurora A degradation by HSP90 interactome-mediating PROTACs in A549 and paclitaxel-resistant A549 cells.
Lung cancer has one of the higher incidence and mortality rates worldwide.
APA
Deng XY, Xu H, et al. (2025). Aurora A degradation by HSP90 interactome-mediating PROTACs in A549 and paclitaxel-resistant A549 cells.. European journal of medicinal chemistry, 300, 118141. https://doi.org/10.1016/j.ejmech.2025.118141
MLA
Deng XY, et al.. "Aurora A degradation by HSP90 interactome-mediating PROTACs in A549 and paclitaxel-resistant A549 cells.." European journal of medicinal chemistry, vol. 300, 2025, pp. 118141.
PMID
40967069
Abstract
Lung cancer has one of the higher incidence and mortality rates worldwide. The development of drug resistance poses a significant challenge to lung cancer treatment. Aurora A kinase, a member of the Aurora family of proteins, has been identified as a key regulator of the cell cycle and mitotic spindle assembly, and overexpression is frequently observed in tumors. Kinase-independent oncogenic functions may be responsible for low clinical response rates, which are difficult to target the conventional small molecules. Targeting both the catalytic and non-catalytic functions of Aurora A may be a viable approach. In this study, we have designed and synthesized a series of novel Aurora A protein degradation-targeted chimeras (Aurora A-PROTACs) based on the HSP90 interactome. Unlike existing Aurora A PROTACs, the new AurAPs series utilizes HSP90, which is highly expressed in tumor cells, as the ligand to recruit the HSP90/E3 ubiquitin ligase complex. AurAPs induced the degradation of the target protein Aurora A by "hijacking" the HSP90/E3 complexes, effectively increasing the targeting of tumors. In vitro biochemical and cellular assays showed that AurAP14 effectively degraded Aurora A kinase, inhibited the proliferation of most human tumor cells and effectively attenuated the development of paclitaxel-resistant lung cancer cells. In addition, AurAP14 significantly inhibited the tumor growth of NSCLC and drug-resistant NSCLC xenograft tumor mice. The results from this study indicate that AurAP14 represents a promising delivery strategy for the sequential elimination of multiple functions of oncogenic proteins and the attenuation of chemotherapy-induced drug resistance.
MeSH Terms
Humans; HSP90 Heat-Shock Proteins; Aurora Kinase A; Paclitaxel; Drug Resistance, Neoplasm; Animals; Cell Proliferation; Mice; Antineoplastic Agents; A549 Cells; Lung Neoplasms; Proteolysis; Molecular Structure; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Structure-Activity Relationship; Protein Kinase Inhibitors; Mice, Nude; Proteolysis Targeting Chimera