Master Transcription Factor Reprogramming Unleashes Selective Translation Promoting Castration Resistance and Immune Evasion in Lethal Prostate Cancer

©2023 The Authors; Published by the American Association for Cancer Research..

Signaling rewiring allows tumors to survive therapy. Here we show that the decrease of the master regulator microphthalmia transcription factor (MITF) in lethal prostate cancer unleashes eukaryotic initiation factor 3B (eIF3B)-dependent translation reprogramming of key mRNAs conferring resistance to androgen deprivation therapy (ADT) and promoting immune evasion. Mechanistically, MITF represses through direct promoter binding eIF3B, which in turn regulates the translation of specific mRNAs. Genome-wide eIF3B enhanced cross-linking immunoprecipitation sequencing (eCLIP-seq) showed specialized binding to a UC-rich motif present in subsets of 5' untranslated regions. Indeed, translation of the androgen receptor and major histocompatibility complex I (MHC-I) through this motif is sensitive to eIF3B amount. Notably, pharmacologic targeting of eIF3B-dependent translation in preclinical models sensitizes prostate cancer to ADT and anti-PD-1 therapy. These findings uncover a hidden connection between transcriptional and translational rewiring promoting therapy-refractory lethal prostate cancer and provide a druggable mechanism that may transcend into effective combined therapeutic strategies.

SIGNIFICANCE: Our study shows that specialized eIF3B-dependent translation of specific mRNAs released upon downregulation of the master transcription factor MITF confers castration resistance and immune evasion in lethal prostate cancer. Pharmacologic targeting of this mechanism delays castration resistance and increases immune-checkpoint efficacy. This article is featured in Selected Articles from This Issue, p. 2489.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:13

Enthalten in:

Cancer discovery - 13(2023), 12 vom: 12. Dez., Seite 2584-2609

Sprache:

Englisch

Beteiligte Personen:

Santasusagna, Sandra [VerfasserIn]
Zhu, Shijia [VerfasserIn]
Jawalagatti, Vijayakumar [VerfasserIn]
Carceles-Cordon, Marc [VerfasserIn]
Ertel, Adam [VerfasserIn]
Garcia-Longarte, Saioa [VerfasserIn]
Song, Won-Min [VerfasserIn]
Fujiwara, Naoto [VerfasserIn]
Li, Peiyao [VerfasserIn]
Mendizabal, Isabel [VerfasserIn]
Petrylak, Daniel P [VerfasserIn]
Kelly, William Kevin [VerfasserIn]
Reddy, E Premkumar [VerfasserIn]
Wang, Liguo [VerfasserIn]
Schiewer, Matthew J [VerfasserIn]
Lujambio, Amaia [VerfasserIn]
Karnes, Jeffrey [VerfasserIn]
Knudsen, Karen E [VerfasserIn]
Cordon-Cardo, Carlos [VerfasserIn]
Dong, Haidong [VerfasserIn]
Huang, Haojie [VerfasserIn]
Carracedo, Arkaitz [VerfasserIn]
Hoshida, Yujin [VerfasserIn]
Rodriguez-Bravo, Veronica [VerfasserIn]
Domingo-Domenech, Josep [VerfasserIn]

Links:

Volltext

Themen:

Androgen Antagonists
Journal Article
Receptors, Androgen
Research Support, N.I.H., Extramural
Transcription Factors

Anmerkungen:

Date Completed 16.12.2023

Date Revised 12.03.2024

published: Print

Citation Status MEDLINE

doi:

10.1158/2159-8290.CD-23-0306

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM361743483