Evidence map›Paper›PMID 28416484›Full record

ArticleCancer research2017

SSRP1 Cooperates with PARP and XRCC1 to Facilitate Single-Strand DNA Break Repair by Chromatin Priming.

Ying Gao, Changling Li, Leizhen Wei, Yaqun Teng, Satoshi Nakajima, Xiukai Chen, Jianquan Xu, Brittany Leger, Hongqiang Ma, Stephen T Spagnol and 5 more

Erratum issuedAbstract read
In one paragraph

Article in Cancer research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 50 citations in OpenAlex.

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  17. SSRP1 Is a Prognostic Biomarker Correlated with CD8BioMed research international · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 1 institution in 1 country.

Ying GaoSchool of Medicine, Tsinghua University, Beijing, China.
Changling LiUniversity of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania.
Leizhen WeiUniversity of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania.
Yaqun TengSchool of Medicine, Tsinghua University, Beijing, China.
Satoshi NakajimaUniversity of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania.
Xiukai ChenUniversity of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania.
Jianquan XuUniversity of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania.
Brittany LegerUniversity of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania.
Hongqiang MaUniversity of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania.
Stephen T SpagnolDepartment of Chemical Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania.
Yong WanUniversity of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania.
Kris Noel DahlDepartment of Chemical Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania.
Yang LiuUniversity of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania.
Arthur S LevineUniversity of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania.
Li LanUniversity of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania. lil64@pitt.edu.
UPMC Hillman Cancer Center · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jessie Nedrow · 1988 to 2026
$158.0M
Transcription-Coupled Homologous Recombination upon DNA DamageR01GM118833 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LAN, LI · 2016 to 2020
$1.6M
Interplay between Cdh1/APC and Rad17 in DNA damage checkpoints and carcinogenesisR01CA154695 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WAN, YONG · 2011 to 2015
$1.5M
Targeting interplay between KLF4 and PRMT5 in carcinogenesisR01CA202963 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WAN, YONG · 2016 to 2020
$1.3M
Oxidative DNA base damage and repair at telomeres and the relevance to cell senesR21AG045545 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LAN, LI, OPRESKO, PATRICIA L · 2013 to 2014
$422k
NCI NIH HHS P30 CA047904NCI NIH HHS R01 CA154695NCI NIH HHS R01 CA202963NIA NIH HHS R21 AG045545NIGMS NIH HHS R01 GM118833
6 · The paper itself

Abstract

DNA single-strand breaks (SSB) are the most common form of DNA damage, requiring repair processes that to initiate must overcome chromatin barriers. The FACT complex comprised of the SSRP1 and SPT16 proteins is important for maintaining chromatin integrity, with SSRP1 acting as an histone H2A/H2B chaperone in chromatin disassembly during DNA transcription, replication, and repair. In this study, we show that SSRP1, but not SPT16, is critical for cell survival after ionizing radiation or methyl methanesulfonate-induced single-strand DNA damage. SSRP1 is recruited to SSB in a PARP-dependent manner and retained at DNA damage sites by N-terminal interactions with the DNA repair protein XRCC1. Mutational analyses showed how SSRP1 function is essential for chromatin decondensation and histone H2B exchange at sites of DNA strand breaks, which are both critical to prime chromatin for efficient SSB repair and cell survival. By establishing how SSRP1 facilitates SSB repair, our findings provide a mechanistic rationale to target SSRP1 as a general approach to selectively attack cancer cells.

Indexed as

DNA Breaks, Single-StrandedDNA RepairBase SequenceCell Line, TumorChromatinDNA-Binding ProteinsHeLa CellsHigh Mobility Group ProteinsHistonesHumansModels, BiologicalPoly(ADP-ribose) PolymerasesProtein BindingProtein Interaction Domains and MotifsSequence Analysis, DNATranscriptional Elongation FactorsChromatinDNA-Binding ProteinsHigh Mobility Group ProteinsHistonesPoly(ADP-ribose) PolymerasesSSRP1 protein, humanTranscriptional Elongation FactorsX-ray Repair Cross Complementing Protein 1XRCC1 protein, human

Identifiers

PMID28416484
PMCPMC5500382
OpenAlexW2607225256

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.