The Effect of p73 Isoforms on DNA Methylation in Cancer Cells (CROSBI ID 637760)
Prilog sa skupa u zborniku | sažetak izlaganja sa skupa
Podaci o odgovornosti
Tučkar, Neven ; Zorić, Arijana ; Horvat, Anđela ; Medvedović, Mario ; Hanžić, Nikolina ; Slade, Neda
engleski
The Effect of p73 Isoforms on DNA Methylation in Cancer Cells
p73 exists in multiple isoforms which could be divided into two groups: one containing transactivation domain (TA) and another amino- terminally truncated (ΔN) isoforms. While TAp73 isoforms show tumor-suppressive functions similar to those of wild-type p53, ΔNp73 isoforms inhibit wild-type p53 as well as TAp63 and TAp73, and are considered as potential oncogenes. ΔNp73 isoforms are overexpressed in many tumors correlating with enhanced chemoresistance and poorer disease outcome. DNA methylation is a form of epigenetic regulation, which adds methyl groups to cytosine residues, regulating gene activity. Hypermethylation of CpG islands in promoter regions inhibits transcription of genes silencing its expression. Using inducible tet-on system, we examined the impact of increased expression of TAp73α and ΔNp73α on global DNA methylation using Illumina Human Methylation 450 BeadChip. Statistically significant change was not found upon induced expression of any p73 isoform.
TP73 ; p73 isoforms ; TAp73α ; ΔNp73α ; methylation
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
Podaci o prilogu
65-65.
2016.
objavljeno
Podaci o matičnoj publikaciji
Game of Epigenomics
Vugrek, Oliver ; Jerić, Ivanka ; Ambriović Ristov, Andreja ; Vidoš, Ana
Zagreb: Institut Ruđer Bošković
978-953-7941-11-6
Podaci o skupu
Game of Epigenomics
poster
24.04.2016-28.04.2016
Dubrovnik, Hrvatska