Neddylation Inhibition Sensitises Renal Medullary Carcinoma Tumours to Platinum Chemotherapy

Authors

Daniel D Shapiro
Niki Millward Zacharias
Durga N Tripathi
Menuka Karki
Jean-Philippe Bertocchio
Melinda Soeung
Rong He
Mary E Westerman
Jianjun Gao
Priya Rao
Truong N A Lam
Eric Jonasch
Luigi Perelli
Emily H Cheng
Alessandro Carugo
Timothy P Heffernan
Cheryl L Walker
Giannicola Genovese
Nizar M Tannir
Jose A Karam
Pavlos Msaouel

Publication Date

5-1-2023

Journal

Clinical and Translational Medicine

Abstract

BACKGROUND: Renal medullary carcinoma (RMC) is a highly aggressive cancer in need of new therapeutic strategies. The neddylation pathway can protect cells from DNA damage induced by the platinum-based chemotherapy used in RMC. We investigated if neddylation inhibition with pevonedistat will synergistically enhance antitumour effects of platinum-based chemotherapy in RMC.

METHODS: We evaluated the IC50 concentrations of the neddylation‐activating enzyme inhibitor pevonedistat in vitro in RMC cell lines. Bliss synergy scores were calculated using growth inhibition assays following treatment with varying concentrations of pevonedistat and carboplatin. Protein expression was assessed by western blot and immunofluorescence assays. The efficacy of pevonedistat alone or in combination with platinum‐based chemotherapy was evaluated in vivo in platinum‐naïve and platinum‐experienced patient‐derived xenograft (PDX) models of RMC.

RESULTS: The RMC cell lines demonstrated IC50 concentrations of pevonedistat below the maximum tolerated dose in humans. When combined with carboplatin, pevonedistat demonstrated a significant in vitro synergistic effect. Treatment with carboplatin alone increased nuclear ERCC1 levels used to repair the interstrand crosslinks induced by platinum salts. Conversely, the addition of pevonedistat to carboplatin led to p53 upregulation resulting in FANCD2 suppression and reduced nuclear ERCC1 levels. The addition of pevonedistat to platinum‐based chemotherapy significantly inhibited tumour growth in both platinum‐naïve and platinum‐experienced PDX models of RMC (p < .01).

CONCLUSIONS: Our results suggest that pevonedistat synergises with carboplatin to inhibit RMC cell and tumour growth through inhibition of DNA damage repair. These findings support the development of a clinical trial combining pevonedistat with platinum-based chemotherapy for RMC.

Keywords

Humans, Carboplatin, Carcinoma, Medullary, Carcinoma, Renal Cell, Kidney Neoplasms

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Supplementary Materials

PMID: 37226898