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bioRxiv · 10.1101/2024.12.11.627923

AKR1C mediates the acquired resistance to T-Dxd in a HER-2 positive gastric cancer line

wang, d.·huang, q.·wang, p.·tang, f.·han, y.·wang, x.·huang, j.·shi, l.·cao, w.·zhang, z.·gu, q.
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Abstract

Trastuzumab deruxtecan (T-Dxd), an anti-HER2 antibody-drug conjugate, has significantly enhanced clinical outcomes for patients as a HER2-directed therapy compared to previous standards of care. However, acquired resistance is always a concern, necessitating further investigation into the underlying resistance mechanism. In this study, we successfully established T-Dxd-resistant cell line (N87-R) by exposing HER2-positive N87 gastric cancer cells to increasing concentrations of T-Dxd, and demonstrated its resistance phenotype both in vitro and in vivo. While there were no changes in HER2 expression or T-Dxd binding in N87-R, a signature of drug metabolism genes were found upregulated, among which AKR1C played a critical role in the resistance mechanism. The resistance phenotype of N87-R cells was mitigated by both siRNA-mediated knockdown of AKR1C and pharmacological inhibition of its enzymatic activity. Our preclinical study underscores the critical role of AKR1C function in mediating T-Dxd resistance and suggests potential therapeutic innovation for combating T-Dxd resistance.

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wang, d., huang, q., wang, p., tang, f., han, y., wang, x., huang, j., shi, l., cao, w., zhang, z., gu, q.. 2024-12-12. AKR1C mediates the acquired resistance to T-Dxd in a HER-2 positive gastric cancer line. https://doi.org/10.1101/2024.12.11.627923

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