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January 20th, 2025
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Weizmann Institute of Science
cancer biology
biorxiv

TMPRSS2-ERG confers resistance to antiandrogens: mechanism and therapeutic implications

Sekar, A.Open in Google Scholar•Chatterjee, R.Open in Google Scholar•Selvadurai, B. R.Open in Google Scholar•Ray, L.Open in Google Scholar•Verma, A.Open in Google Scholar•Nataraj, N. B.Open in Google Scholar•Garcia, D. D.Open in Google Scholar•Giri, S.Open in Google Scholar•Genna, A.Open in Google Scholar•Karatekin, F.Open in Google Scholaret al.

Approximately 50% of prostate cancer (PCa) patients harbor fusions involving the TMPRSS2 and ERG genes. Despite this, tailored therapies targeting the fused gene, tERG, remain undeveloped. Our study analyzed biopsy samples from two clinical trials assessing the efficacies of androgen receptor (AR) signaling inhibitors (ARSIs). The results revealed that tERG promotes resistance to ARSIs and is associated with elevated levels of the glucocorticoid receptor (GR). Subsequent assays showed that GR directly interacts with tERG, alleviates allosteric autoinhibition and prevents chemotherapy-induced tERG degradation. In PCa models, either inhibiting GR or lowering cortisol levels suppressed tumor growth in tERG-positive models, but not in fusion-negative models. In addition, patient-derived fusion-positive xenografts displayed enhanced sensitivity to combined GR and AR inhibitors. Collectively, these findings highlight TMPRSS2-ERG as a new biomarker and propose that simultaneous inhibition of GR and AR may specifically benefit tERG-positine patients. However, GR stimulatory corticosteroid therapies may not be advisable for this patient subgroup.

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