Evidence map›Paper›PMID 39728924›Full record

ArticleeLife2024

Telomere length sensitive regulation of interleukin receptor 1 type 1 (IL1R1) by the shelterin protein TRF2 modulates immune signalling in the tumour microenvironment.

Ananda Kishore Mukherjee, Subhajit Dutta, Ankita Singh, Shalu Sharma, Shuvra Shekhar Roy, Antara Sengupta, Megha Chatterjee, Soujanya Vinayagamurthy, Sulochana Bagri, Divya Khanna and 11 more

Abstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
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

21 authors.

Ananda Kishore MukherjeeIntegrative and Functional Biology Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.ORCID https://orcid.org/0000-0002-3082-6749
Subhajit Dutta *Integrative and Functional Biology Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Ankita Singh *Integrative and Functional Biology Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Shalu SharmaIntegrative and Functional Biology Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Shuvra Shekhar RoyIntegrative and Functional Biology Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Antara SenguptaIntegrative and Functional Biology Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Megha ChatterjeeIntegrative and Functional Biology Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Soujanya VinayagamurthyIntegrative and Functional Biology Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.ORCID https://orcid.org/0000-0003-1465-9925
Sulochana BagriIntegrative and Functional Biology Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.ORCID https://orcid.org/0000-0001-7407-2558
Divya KhannaIntegrative and Functional Biology Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Meenakshi VermaIntegrative and Functional Biology Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Dristhi SoniIntegrative and Functional Biology Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Anshul BudharajaIIT Delhi, Delhi, India.
Sagar Kailasrao BhisadeIISER Bhopal, Bhopal, India.
Vivek AnandAcademy of Scientific and Innovative Research (AcSIR), Ghaziabad, India.
Ahmad PerwezIntegrative and Functional Biology Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Nija GeorgeNational Centre for Biological Sciences, Tata Institute of Fundamental Research, Bangalore, India.
Mohammed FaruqAcademy of Scientific and Innovative Research (AcSIR), Ghaziabad, India.
Ishaan GuptaIIT Delhi, Delhi, India.
Radhakrishnan SabarinathanGNR Knowledge Centre for Genome and Informatics, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Shantanu ChowdhuryIntegrative and Functional Biology Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.ORCID https://orcid.org/0000-0001-7185-8408

Funding

DBT-Wellcome Trust India Alliance IA/S/18/2/504021Wellcome TrustWellcome Trust DBt India Alliance IA/S/18/2/504021
6 · The paper itself

Abstract

Telomeres are crucial for cancer progression. Immune signalling in the tumour microenvironment has been shown to be very important in cancer prognosis. However, the mechanisms by which telomeres might affect tumour immune response remain poorly understood. Here, we observed that interleukin-1 signalling is telomere-length dependent in cancer cells. Mechanistically, non-telomeric TRF2 (telomeric repeat binding factor 2) binding at the IL-1-receptor type-1 (IL1R1) promoter was found to be affected by telomere length. Enhanced TRF2 binding at the

Indexed as

Signal TransductionTelomereTelomeric Repeat Binding Protein 2Tumor MicroenvironmentAnimalsCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansMicePromoter Regions, GeneticReceptors, Interleukin-1 Type ITriple Negative Breast NeoplasmsIL1R1 protein, humanReceptors, Interleukin-1 Type ITelomeric Repeat Binding Protein 2TERF2 protein, humancancer biologychromosomesgene expressionhumaninterleukin-1 signallingmousetelomeretelomeric repeat binding factor 2TNBCTRF2triple-negative breast cancertumour immunitytumour macrophages

Identifiers

PMID39728924
PMCPMC11677240

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.