G-quadruplexes: a promising target for cancer therapy

N Kosiol, S Juranek, P Brossart, A Heine, K Paeschke - Molecular Cancer, 2021 - Springer
DNA and RNA can fold into a variety of alternative conformations. In recent years, a
particular nucleic acid structure was discussed to play a role in malignant transformation and …

Recent Update on Targeting c-MYC G-Quadruplexes by Small Molecules for Anticancer Therapeutics

R Chaudhuri, S Bhattacharya, J Dash… - Journal of Medicinal …, 2020 - ACS Publications
Guanine-rich DNA sequences have the propensity to adopt four-stranded tetrahelical G-
quadruplex (G4) structures that are overrepresented in gene promoters. The structural …

Small-molecule quadruplex-targeted drug discovery

SA Ohnmacht, S Neidle - Bioorganic & medicinal chemistry letters, 2014 - Elsevier
Repeated guanine tracts in human and other genomes can form higher-order four stranded
structures, termed quadruplexes. In the human genome they have particular prevalence in …

Human MYC G-quadruplex: From discovery to a cancer therapeutic target

W Wang, S Hu, Y Gu, Y Yan, DB Stovall, D Li… - Biochimica et Biophysica …, 2020 - Elsevier
Overexpression of the MYC oncogene is a molecular hallmark of both cancer initiation and
progression. Targeting MYC is a logical and effective cancer therapeutic strategy. A special …

Experimental methods for studying the interactions between G-quadruplex structures and ligands

J Jaumot, R Gargallo - Current pharmaceutical design, 2012 - ingentaconnect.com
The present paper reviews the recent advances in and applications of experimental
techniques used to study interactions between G-quadruplex structures and ligands that are …

Anticancer activity and cellular repression of c-MYC by the G-quadruplex-stabilizing 11-piperazinylquindoline is not dependent on direct targeting of the G-quadruplex …

PVL Boddupally, S Hahn, C Beman, B De… - Journal of medicinal …, 2012 - ACS Publications
This G-rich region of the c-MYC promoter has been shown to form a G-quadruplex structure
that acts as a silencer element for c-MYC transcriptional control. In the present work, we …

Discovery of Novel 11-Triazole Substituted Benzofuro[3,2-b]quinolone Derivatives as c-myc G-Quadruplex Specific Stabilizers via Click Chemistry

DY Zeng, GT Kuang, SK Wang, W Peng… - Journal of Medicinal …, 2017 - ACS Publications
The specificity of nucleic acids' binders is crucial for developing this kind of drug, especially
for novel G-quadruplexes' binders. Quindoline derivatives have been developed as G …

G-quadruplex binding ligands: from naturally occurring to rationally designed molecules

T Vy Thi Le, S Han, J Chae… - Current pharmaceutical …, 2012 - ingentaconnect.com
Guanine-rich nucleic acid sequences are known to form G-quadruplex-four-stranded DNA or
RNA structures stabilized by an array of Hoogsteen hydrogen bonds. G-quadruplex …

Targeting G-quadruplex nucleic acids with heterocyclic alkaloids and their derivatives

YX Xiong, ZS Huang, JH Tan - European journal of medicinal chemistry, 2015 - Elsevier
G-Quadruplex nucleic acids or G-quadruplexes (G4s) are four-stranded DNA or RNA
secondary structures that are formed in guanine-rich sequences. They are widely distributed …

Berberine: a promising natural isoquinoline alkaloid for the development of hypolipidemic drugs

DD Li, P Yu, W Xiao, ZZ Wang… - Current Topics in …, 2020 - ingentaconnect.com
Berberine, as a representative isoquinoline alkaloid, exhibits significant hypolipidemic
activity in both animal models and clinical trials. Recently, a large number of studies on the …