Translation reprogramming is an evolutionarily conserved driver of phenotypic plasticity and therapeutic resistance in melanoma
The intra-tumour microenvironment generates phenotypically distinct but inter-convertible malignant cell subpopulations that fuel metastatic spread and therapeutic-resistance. Whether different microenvironmental cues impose invasive or therapy-resistant phenotypes via a common mechanism is unknown....
Main Authors: | Falletta, P, Sanchez-del-Campo, L, Chauhan, J, Effern, M, Kenyon, A, Kershaw, C, Siddaway, R, Lisle, R, Freter, R, Daniels, M, Lu, X, Tüting, T, Middleton, M, Buffa, F, Willis, A, Pavitt, G, Ronai, Z, Sauka-Spengler, T, Hölzel, M, Goding, C |
---|---|
Format: | Journal article |
Published: |
Cold Spring Harbor Laboratory Press
2017
|
Similar Items
-
MITF controls the TCA cycle to modulate the melanoma hypoxia response
by: Louphrasitthiphol, P, et al.
Published: (2019) -
The MITF regulatory network in melanoma
by: Chauhan, JS, et al.
Published: (2022) -
Establishment of a fluorescent reporter of RNA-polymerase II activity to identify dormant cells
by: Freter, R, et al.
Published: (2021) -
Lineage-restricted regulation of SCD and fatty acid saturation by MITF controls melanoma phenotypic plasticity
by: Vivas-García, Y, et al.
Published: (2019) -
BRN2 suppresses apoptosis, reprograms DNA damage repair, and is associated with a high somatic mutation burden in melanoma
by: Herbert, K, et al.
Published: (2019)