TY - JOUR
T1 - An epitranscriptomic mechanism underlies selective mRNA translation remodelling in melanoma persister cells
AU - Shen, Shensi
AU - Faouzi, Sara
AU - Bastide, Amandine
AU - Martineau, Sylvain
AU - Malka-Mahieu, Hélène
AU - Fu, Yu
AU - Sun, Xiaoxiao
AU - Mateus, Christine
AU - Routier, Emilie
AU - Roy, Severine
AU - Desaubry, Laurent
AU - André, Fabrice
AU - Eggermont, Alexander
AU - David, Alexandre
AU - Scoazec, Jean Yves
AU - Vagner, Stéphan
AU - Robert, Caroline
N1 - Publisher Copyright:
© 2019, The Author(s).
PY - 2019/12/1
Y1 - 2019/12/1
N2 - Cancer persister cells tolerate anticancer drugs and serve as the founders of acquired resistance and cancer relapse. Here we show that a subpopulation of BRAFV600 mutant melanoma cells that tolerates exposure to BRAF and MEK inhibitors undergoes a reversible remodelling of mRNA translation that evolves in parallel with drug sensitivity. Although this process is associated with a global reduction in protein synthesis, a subset of mRNAs undergoes an increased efficiency in translation. Inhibiting the eIF4A RNA helicase, a component of the eIF4F translation initiation complex, abrogates this selectively increased translation and is lethal to persister cells. Translation remodelling in persister cells coincides with an increased N6-methyladenosine modification in the 5′-untranslated region of some highly translated mRNAs. Combination of eIF4A inhibitor with BRAF and MEK inhibitors effectively inhibits the emergence of persister cells and may represent a new therapeutic strategy to prevent acquired drug resistance.
AB - Cancer persister cells tolerate anticancer drugs and serve as the founders of acquired resistance and cancer relapse. Here we show that a subpopulation of BRAFV600 mutant melanoma cells that tolerates exposure to BRAF and MEK inhibitors undergoes a reversible remodelling of mRNA translation that evolves in parallel with drug sensitivity. Although this process is associated with a global reduction in protein synthesis, a subset of mRNAs undergoes an increased efficiency in translation. Inhibiting the eIF4A RNA helicase, a component of the eIF4F translation initiation complex, abrogates this selectively increased translation and is lethal to persister cells. Translation remodelling in persister cells coincides with an increased N6-methyladenosine modification in the 5′-untranslated region of some highly translated mRNAs. Combination of eIF4A inhibitor with BRAF and MEK inhibitors effectively inhibits the emergence of persister cells and may represent a new therapeutic strategy to prevent acquired drug resistance.
UR - http://www.scopus.com/inward/record.url?scp=85076619587&partnerID=8YFLogxK
U2 - 10.1038/s41467-019-13360-6
DO - 10.1038/s41467-019-13360-6
M3 - Article
C2 - 31844050
AN - SCOPUS:85076619587
SN - 2041-1723
VL - 10
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 5713
ER -