Can THEM6 targeting stop resistance to prostate cancer treatment?
- PMID: 35107853
- PMCID: PMC8899918
- DOI: 10.15252/emmm.202115504
Can THEM6 targeting stop resistance to prostate cancer treatment?
Abstract
Prostate cancer (PCa) clinical management relies heavily on androgen-deprivation therapy (ADT). However, despite experiencing initial clinical benefit, patients getting ADT for non-resectable PCa eventually relapse and develop fatal castration-resistant PCa (CRPC). Multiple mechanisms of acquired resistance to treatment have been reported, including metabolic adaptation (Marine et al, 2020). Notably, activation of the endoplasmic reticulum (ER) unfolded protein response (UPR) has been associated with oncogenic transformation (Hart et al, 2012), tumor progression, metastasis dissemination, and resistance to therapy (Chen & Cubillos-Ruiz, 2021). Targeting different branches of ER UPR has been found to be an effective tool against aggressive PCa (Nguyen et al, 2018; Sheng et al, 2019). Therefore, a better understanding of these pathways may lead to the identification of novel drug targets.
© 2022 The Authors. Published under the terms of the CC BY 4.0 license.
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Comment on
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THEM6-mediated reprogramming of lipid metabolism supports treatment resistance in prostate cancer.EMBO Mol Med. 2022 Mar 7;14(3):e14764. doi: 10.15252/emmm.202114764. Epub 2022 Jan 11. EMBO Mol Med. 2022. PMID: 35014179 Free PMC article.
References
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- Marine JC, Dawson SJ, Dawson MA (2020) Non‐genetic mechanisms of therapeutic resistance in cancer. Nat Rev Cancer 20: 743–756 - PubMed
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