scholarly journals A Nucleus-Imaging Probe That Selectively Stabilizes a Minor Conformation of c-MYC G-quadruplex and Down-regulates c-MYC Transcription in Human Cancer Cells

2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Deepanjan Panda ◽  
Manish Debnath ◽  
Samir Mandal ◽  
Irene Bessi ◽  
Harald Schwalbe ◽  
...  
2020 ◽  
Vol 63 (6) ◽  
pp. 3090-3103 ◽  
Author(s):  
Jussara Amato ◽  
Giulia Miglietta ◽  
Rita Morigi ◽  
Nunzia Iaccarino ◽  
Alessandra Locatelli ◽  
...  

2018 ◽  
Author(s):  
Alessio De Magis ◽  
Stefano Giustino Manzo ◽  
Marco Russo ◽  
Olivier Sordet ◽  
Rita Morigi ◽  
...  

RSC Advances ◽  
2020 ◽  
Vol 10 (44) ◽  
pp. 26388-26396
Author(s):  
Soumi Biswas ◽  
Satyabrata Samui ◽  
Apurba K. Das ◽  
Sanjeev Pasadi ◽  
K. Muniyappa ◽  
...  

A synthetic dendritic peptide, targeting human telomeric G4 DNA, inhibits the telomerase and lessens the proliferation of human cancer cells.


RSC Advances ◽  
2017 ◽  
Vol 7 (82) ◽  
pp. 51965-51969 ◽  
Author(s):  
Fengmin Yang ◽  
Xin Sun ◽  
Lixia Wang ◽  
Qian Li ◽  
Aijiao Guan ◽  
...  

Indolizinone could selectively recognize c-myc promoter G-quadruplex.


2022 ◽  
Vol 12 (1) ◽  
Author(s):  
Winnie W. I. Hui ◽  
Angela Simeone ◽  
Katherine G. Zyner ◽  
David Tannahill ◽  
Shankar Balasubramanian

2018 ◽  
Vol 116 (3) ◽  
pp. 816-825 ◽  
Author(s):  
Alessio De Magis ◽  
Stefano G. Manzo ◽  
Marco Russo ◽  
Jessica Marinello ◽  
Rita Morigi ◽  
...  

G quadruplexes (G4s) and R loops are noncanonical DNA structures that can regulate basic nuclear processes and trigger DNA damage, genome instability, and cell killing. By different technical approaches, we here establish that specific G4 ligands stabilize G4s and simultaneously increase R-loop levels within minutes in human cancer cells. Genome-wide mapping of R loops showed that the studied G4 ligands likely cause the spreading of R loops to adjacent regions containing G4 structures, preferentially at 3′-end regions of expressed genes, which are partially ligand-specific. Overexpression of an exogenous human RNaseH1 rescued DNA damage induced by G4 ligands in BRCA2-proficient and BRCA2-silenced cancer cells. Moreover, even if the studied G4 ligands increased noncanonical DNA structures at similar levels in nuclear chromatin, their cellular effects were different in relation to cell-killing activity and stimulation of micronuclei, a hallmark of genome instability. Our findings therefore establish that G4 ligands can induce DNA damage by an R loop-dependent mechanism that can eventually lead to different cellular consequences depending on the chemical nature of the ligands.


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