Evidence map›Paper›PMID 32093313›Full record

ArticleInternational journal of molecular sciences2020

TLR3 Expression Induces Apoptosis in Human Non-Small-Cell Lung Cancer.

Francesca Bianchi, Spyridon Alexiadis, Chiara Camisaschi, Mauro Truini, Giovanni Centonze, Massimo Milione, Andrea Balsari, Elda Tagliabue, Lucia Sfondrini

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

37 citing papers in PubMed, 59 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 3 institutions in 1 country.

Francesca BianchiMolecular Targeting Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133 Milan, Italy.ORCID 0000-0001-5197-5279
Spyridon AlexiadisPathological Anatomy Unit, ASST Grande Ospedale Metropolitano Niguarda, 20162 Milan, Italy.
Chiara CamisaschiImmunotherapy of Human Tumors Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133 Milan, Italy.ORCID 0000-0002-5205-919X
Mauro TruiniPathological Anatomy Unit, ASST Grande Ospedale Metropolitano Niguarda, 20162 Milan, Italy.
Giovanni CentonzeFirst Pathology Unit, Department of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133 Milan, Italy.ORCID 0000-0003-2864-7941
Massimo MilioneFirst Pathology Unit, Department of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133 Milan, Italy.
Andrea BalsariDipartimento di Scienze Biomediche per la Salute, Università degli Studi di Milano, 20133 Milan, Italy.
Elda TagliabueMolecular Targeting Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133 Milan, Italy.ORCID 0000-0001-9877-2903
Lucia SfondriniDipartimento di Scienze Biomediche per la Salute, Università degli Studi di Milano, 20133 Milan, Italy.
Fondazione IRCCS Istituto Nazionale dei Tumori · ITAzienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda · ITUniversity of Milan · IT

Funding

Associazione Italiana per la Ricerca sul Cancro IG 15190 to Andrea BalsariFondazione Umberto Veronesi Fellowships 2017, 2018 and 2019 to FB
6 · The paper itself

Abstract

The prognostic value of Toll-like receptor 3 (TLR3) is debated in cancer, differing between tumor types, methods, and cell types. We recently showed for the first time that TLR3 expression on early stage non-small-cell lung cancer (NSCLC) results associated with a good prognosis. Here, we provide experimental evidences explaining the molecular reason behind TLR3's favorable prognostic role. We demonstrated that TLR3 activation in vitro induces apoptosis in lung cancer cell lines and, accordingly, that TLR3 expression is associated with caspase-3 activation in adenocarcinoma NSCLC specimens, both evaluated by immunohistochemistry. Moreover, we showed that TLR3 expression on cancer cells contributes to activate the CD103+ lung dendritic cell subset, that is specifically associated with processing of antigens derived from apoptotic cells and their presentation to CD8+ T lymphocytes. These findings point to the relevant role of TLR3 expression on lung cancer cells and support the use of TLR3 agonists in NSCLC patients to re-activate local innate immune response.

Indexed as

AnimalsApoptosisCarcinoma, Non-Small-Cell LungCaspase 3Cell Line, TumorGene Expression Regulation, NeoplasticHumansImmunity, InnateImmunotherapyLung NeoplasmsMiceNeoplasm ProteinsToll-Like Receptor 3CASP3 protein, humanCaspase 3Neoplasm ProteinsTLR3 protein, humanToll-Like Receptor 3apoptosisCD103dendritic cellsIHCNSCLCpoly(I:C)toll-like receptor 3 (TLR3)

Identifiers

PMID32093313
PMCPMC7073031
OpenAlexW3007889593

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.