TY - JOUR
T1 - G-quadruplex forming motifs in the promoter region of the B-MYB proto-oncogene
AU - Miranda, André
AU - Cucchiarini, Anne
AU - Esnault, Cyril
AU - Andrau, Jean Christophe
AU - Oliveira, Paula A.
AU - Mergny, Jean Louis
AU - Cruz, Carla
N1 - Publisher Copyright:
© 2023
PY - 2024/6/1
Y1 - 2024/6/1
N2 - To combat cancer, a comprehensive understanding of the molecular mechanisms and behaviors involved in carcinogenesis is crucial, as tumorigenesis is a complex process influenced by various genetic events and disease hallmarks. The B-MYB gene encodes a transcription factor involved in cell cycle regulation, survival, and differentiation in normal cells. B-MYB can be transformed into an oncogene through mutations, and abnormal expression of B-MYB has been identified in various cancers, including lung cancer, and is associated with poor prognosis. Targeting this oncogene is a promising approach for anti-cancer drug design. B-MYB has been deemed undruggable in previous reports, necessitating the search for novel therapeutic options. In this study, we found that the B-MYB gene promoter contains several G/C rich motifs compatible with G-quadruplex (G4) formation. We investigated and validated the existence of G4 structures in the promoter region of B-MYB, first in vitro using a combination of bioinformatics, biophysical, and biochemical methods, then in cell with the recently developed G4access method.
AB - To combat cancer, a comprehensive understanding of the molecular mechanisms and behaviors involved in carcinogenesis is crucial, as tumorigenesis is a complex process influenced by various genetic events and disease hallmarks. The B-MYB gene encodes a transcription factor involved in cell cycle regulation, survival, and differentiation in normal cells. B-MYB can be transformed into an oncogene through mutations, and abnormal expression of B-MYB has been identified in various cancers, including lung cancer, and is associated with poor prognosis. Targeting this oncogene is a promising approach for anti-cancer drug design. B-MYB has been deemed undruggable in previous reports, necessitating the search for novel therapeutic options. In this study, we found that the B-MYB gene promoter contains several G/C rich motifs compatible with G-quadruplex (G4) formation. We investigated and validated the existence of G4 structures in the promoter region of B-MYB, first in vitro using a combination of bioinformatics, biophysical, and biochemical methods, then in cell with the recently developed G4access method.
KW - B-MYB proto-oncogene
KW - G-quadruplex formation
KW - In vitro analysis
U2 - 10.1016/j.ijbiomac.2024.132244
DO - 10.1016/j.ijbiomac.2024.132244
M3 - Article
C2 - 38729459
AN - SCOPUS:85192929069
SN - 0141-8130
VL - 270
JO - International Journal of Biological Macromolecules
JF - International Journal of Biological Macromolecules
M1 - 132244
ER -