Evidence map›Paper›PMID 25589350›Full record

ArticleCancer research2015

Single-strand DNA-binding protein SSB1 facilitates TERT recruitment to telomeres and maintains telomere G-overhangs.

Raj K Pandita, Tracy T Chow, Durga Udayakumar, Amanda L Bain, Liza Cubeddu, Clayton R Hunt, Wei Shi, Nobuo Horikoshi, Yong Zhao, Woodring E Wright and 3 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 3 countries.

Raj K PanditaDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas. Department of Radiation Oncology, The Houston Methodist Research Institute, Houston, Texas.
Tracy T ChowDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas.
Durga UdayakumarDepartment of Radiation Oncology, The Houston Methodist Research Institute, Houston, Texas. Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, Texas.
Amanda L BainQIMR Berghofer Medical Research Institute, Herston, Brisbane, Australia.
Liza CubedduSchool of Science and Health, University of Western Sydney, Sydney, Australia.
Clayton R HuntDepartment of Radiation Oncology, The Houston Methodist Research Institute, Houston, Texas. Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, Texas.
Wei ShiQIMR Berghofer Medical Research Institute, Herston, Brisbane, Australia.
Nobuo HorikoshiDepartment of Radiation Oncology, The Houston Methodist Research Institute, Houston, Texas. Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, Texas.
Yong ZhaoDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas.
Woodring E WrightDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas.
Kum Kum KhannaQIMR Berghofer Medical Research Institute, Herston, Brisbane, Australia.
Jerry W ShayDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas. Center for Excellence in Genomics Medicine Research, King Abdulaziz University, Jeddah, Saudi Arabia. tpandita@houstonmethodist.org jerry.shay@utsouthwestern.edu.
Tej K PanditaDepartment of Radiation Oncology, The Houston Methodist Research Institute, Houston, Texas. Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, Texas. tpandita@houstonmethodist.org jerry.shay@utsouthwestern.edu.
Houston Methodist · USQIMR Berghofer Medical Research Institute · AUThe University of Texas Southwestern Medical Center · USKing Abdulaziz University · SAWestern Sydney University · AU

Funding

CHROMATIN MODIFYING FACTORS CONTROL RADIATION RESPONSE AND GENOMIC STABILITYR01CA129537 · NCI · WASHINGTON UNIVERSITY · PI PANDITA, TEJ K · 2008 to 2018
$3.3M
Tumor-cell-specific targets for combined hyperthermia and radiation effectsR01CA154320 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI PANDITA, TEJ K · 2010 to 2014
$1.6M
Role of Heterochromatin protein 1 Beta in Genome Maintenance and OncogenesisR01GM109768 · NIGMS · METHODIST HOSPITAL RESEARCH INSTITUTE · PI PANDITA, TEJ K · 2014 to 2017
$1.2M
NCI NIH HHS CA129537NCI NIH HHS CA154320NCI NIH HHS R01 CA129537NCI NIH HHS R01 CA154320NIGMS NIH HHS GM109768NIGMS NIH HHS R01 GM109768
6 · The paper itself

Abstract

Proliferating mammalian stem and cancer cells express telomerase [telomerase reverse transcriptase (TERT)] in an effort to extend chromosomal G-overhangs and maintain telomere ends. Telomerase-expressing cells also have higher levels of the single-stranded DNA-binding protein SSB1, which has a critical role in DNA double-strand break (DSB) repair. Here, we report that SSB1 binds specifically to G-strand telomeric DNA in vitro and associates with telomeres in vivo. SSB1 interacts with the TERT catalytic subunit and regulates its interaction with telomeres. Deletion of SSB1 reduces TERT interaction with telomeres and leads to G-overhang loss. Although SSB1 is recruited to DSB sites, we found no corresponding change in TERT levels at these sites, implying that SSB1-TERT interaction relies upon a specific chromatin structure or context. Our findings offer an explanation for how telomerase is recruited to telomeres to facilitate G-strand DNA extension, a critical step in maintaining telomere ends and cell viability in all cancer cells. Cancer Res; 75(5); 858-69. ©2015 AACR.

Indexed as

AnimalsDNA-Binding ProteinsDNA DamageDNA, Single-StrandedHCT116 CellsHEK293 CellsHumansMiceMice, KnockoutMitochondrial ProteinsProtein BindingS PhaseTelomeraseTelomereTelomeric Repeat Binding Protein 1DNA-Binding ProteinsDNA, Single-StrandedMitochondrial ProteinsNABP2 protein, humanTelomeraseTelomeric Repeat Binding Protein 1

Identifiers

PMID25589350
PMCPMC4351820
OpenAlexW2158941313

What OpenQuestion holds

Textmetadata
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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.