Evidence map›Paper›PMID 35736637›Full record

ArticleNon-coding RNA2022

LINC00892 Is an lncRNA Induced by T Cell Activation and Expressed by Follicular Lymphoma-Resident T Helper Cells.

Ingram Iaccarino, Fatme Mourtada, Sarah Reinke, Paurnima Patil, Gero Doose, Gianni Monaco, Steve Hoffmann, Reiner Siebert, Wolfram Klapper

Open access · goldAbstract read
In one paragraph

Article in Non-coding RNA, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

11 citing papers in PubMed, 9 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

9 authors at 4 institutions in 2 countries.

Ingram IaccarinoDepartment of Pathology, Hematopathology Section and Lymph Node Registry, University of Kiel, 24105 Kiel, Germany.ORCID 0000-0001-7324-993X
Fatme MourtadaDepartment of Pathology, Hematopathology Section and Lymph Node Registry, University of Kiel, 24105 Kiel, Germany.
Sarah ReinkeDepartment of Pathology, Hematopathology Section and Lymph Node Registry, University of Kiel, 24105 Kiel, Germany.ORCID 0000-0001-9729-4030
Paurnima PatilInstitute of Human Genetics, Ulm University, Ulm University Medical Center, 89081 Ulm, Germany.
Gero DooseecSeq Bioinformatics GmbH, 04103 Leipzig, Germany.
Gianni MonacoInstitute for Transfusion Medicine and Gene Therapy, Medical Center-University of Freiburg, 79106 Freiburg, Germany.
Steve HoffmannLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), 07745 Jena, Germany.
Reiner SiebertInstitute of Human Genetics, Ulm University, Ulm University Medical Center, 89081 Ulm, Germany.
Wolfram KlapperDepartment of Pathology, Hematopathology Section and Lymph Node Registry, University of Kiel, 24105 Kiel, Germany.
Christian-Albrechts-Universität zu Kiel · DEUniversität Ulm · DELeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DEUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Successful immunotherapy in both solid tumors and in hematological malignancies relies on the ability of T lymphocytes to infiltrate the cancer tissue and mount an immune response against the tumor. Biomarkers able to discern the amount and the types of T lymphocytes infiltrating a given tumor therefore have high diagnostic and prognostic value. Given that lncRNAs are known to have a highly cell-type-specific expression pattern, we searched for lncRNAs specifically expressed by activated T cells and at the same time in a kind of lymphoma, follicular lymphoma, where the microenvironment is known to play a critical role in the regulation of antitumor immunity. We focused on a non-coding transcript, annotated as LINC00892, which reaches extremely high expression levels following cell activation in Jurkat cells. Interestingly LINC00892 has an expression pattern resembling that of genes involved in T cell memory. Accordingly, LINC00892 is mostly expressed by the effector memory and helper CD4+ T cell sub-types but not by naïve T cells. In situ analyses of LINC00892 expression in normal lymph nodes and in follicular lymphoma biopsies show that its expression is limited to CD4+ PD1

Indexed as

Follicular LymphomaLINC00892lncRNAPD1T cell activationT helper cells

Identifiers

PMID35736637
PMCPMC9228450
OpenAlexW4281729406

What OpenQuestion holds

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LicenceCC BY
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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.