2015
DOI: 10.1080/15384101.2015.1049784
|View full text |Cite
|
Sign up to set email alerts
|

A role for homologous recombination proteins in cell cycle regulation

Abstract: Eukaryotic cells respond to DNA breaks, especially double-stranded breaks (DSBs), by activating the DNA damage response (DDR), which encompasses DNA repair and cell cycle checkpoint signaling. The DNA damage signal is transmitted to the checkpoint machinery by a network of specialized DNA damage-recognizing and signal-transducing molecules. However, recent evidence suggests that DNA repair proteins themselves may also directly contribute to the checkpoint control. Here, we investigated the role of homologous r… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

1
13
1

Year Published

2015
2015
2023
2023

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 23 publications
(15 citation statements)
references
References 51 publications
1
13
1
Order By: Relevance
“…Our results indicate that a higher gene expression of BRCA1 is highly associated with increasing clinical malignancy (indicated by higher IMIG-stage). Furthermore, a reduced XRCC2 gene expression, acting downstream of the MRN-complex 95 , correlated with with progressive disease more often. Similarly, increased XRCC3 gene expression, forming a complex together with XRCC2 , was observed in tumours showing higher TNM-stage.…”
Section: Discussionmentioning
confidence: 94%
“…Our results indicate that a higher gene expression of BRCA1 is highly associated with increasing clinical malignancy (indicated by higher IMIG-stage). Furthermore, a reduced XRCC2 gene expression, acting downstream of the MRN-complex 95 , correlated with with progressive disease more often. Similarly, increased XRCC3 gene expression, forming a complex together with XRCC2 , was observed in tumours showing higher TNM-stage.…”
Section: Discussionmentioning
confidence: 94%
“…S2A). Cells were re‐transfected 72 h later with pGEGFP or p1‐68‐GFP, and pSVpuro, using Lipofectamine 2000 (Invitrogen), once the effects of the knock‐down on cell cycle progression had disappeared (Kostyrko et al, ). The cells were trypsinized and counted 24 h after the second transfection, and 10000 viable cells were seeded in complete medium into each well of a 6‐well plate.…”
Section: Methodsmentioning
confidence: 99%
“…Furthermore, a CHO‐DG44 derivative with FUCCI was used in a study elucidating the role of homologous recombination proteins in cell cycle regulation . However, no project targeting real time compatible detection of the growth rate was reported, yet …”
Section: Introductionmentioning
confidence: 99%