Evidence map›Paper›PMID 32619407›Full record

ArticleCancer cell2020

Telomere Stress Potentiates STING-Dependent Anti-tumor Immunity.

Ilgen Mender, Anli Zhang, Zhenhua Ren, Chuanhui Han, Yafang Deng, Silvia Siteni, Huiyu Li, Jiankun Zhu, Aishwarya Vemula, Jerry W Shay and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 3% 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

84 citing papers in PubMed, 1 synthesis or guideline pooled it, 162 citations in OpenAlex.

  1. Pooled it
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  12. Cell-selective telomere damage by thiopurine-based oligonucleotide for diffuse large B cell lymphoma immunotherapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
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24 more citing papers are in PubMed but not listed here.

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

11 authors at 3 institutions in 1 country.

Ilgen MenderDepartment of Cell Biology, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Anli ZhangDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX 75390, USA. Electronic address: anli.zhang@utsouthwestern.edu.
Zhenhua RenDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Chuanhui HanDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Yafang DengDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Silvia SiteniDepartment of Cell Biology, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Huiyu LiHamon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Jiankun ZhuDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Aishwarya VemulaDepartment of Cell Biology, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Jerry W ShayDepartment of Cell Biology, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Yang-Xin FuDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Southwestern Medical CenterThe University of Texas Southwestern Medical Center · USSouthwestern Medical Center · US

Funding

UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI BYERS, LAUREN AVERETT · 1996 to 2024
$57.4M
Cell Biology Research Improvements and RenovationsC06RR030414 · NCRR · UT SOUTHWESTERN MEDICAL CENTER · PI FITZ, JOHN GREGORY · 2010 to 2010
$15.0M
Cancer Biology Training GrantT32CA124334 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI SHAY, JERRY WILLIAM · 2007 to 2021
$5.3M
NCI NIH HHS P50 CA070907NCI NIH HHS T32 CA124334NCRR NIH HHS C06 RR030414
6 · The paper itself

Abstract

Telomerase is an attractive target for anti-tumor therapy as it is almost universally expressed in cancer cells. Here, we show that treatment with a telomere-targeting drug, 6-thio-2'-deoxyguanosine (6-thio-dG), leads to tumor regression through innate and adaptive immune-dependent responses in syngeneic and humanized mouse models of telomerase-expressing cancers. 6-thio-dG treatment causes telomere-associated DNA damages that are sensed by dendritic cells (DCs) and activates the host cytosolic DNA sensing STING/interferon I pathway, resulting in enhanced cross-priming capacity of DCs and tumor-specific CD8

Indexed as

Adaptive ImmunityAnimalsCD8-Positive T-LymphocytesCell Line, TumorDeoxyguanosineHCT116 CellsHumansImmunity, InnateMembrane ProteinsMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutNeoplasmsNeoplasms, ExperimentalSignal TransductionSTING Proteinalpha-2'-deoxythioguanosineDeoxyguanosineMembrane ProteinsSTING1 protein, humanSTING ProteinTelomeraseThionucleosides6-thio-dGanti-tumor immunitycheckpoint blockadeDNA damageimmunotherapyinnate sensingPD-1/PD-L1STINGtelomerasetelomere-targeting therapy

Identifiers

PMID32619407
PMCPMC7494563
OpenAlexW3039849639

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.