Evidence map›Paper›PMID 33923020›Full record

ArticleCancers2021

TLR4-Mediated Recognition of Mouse Polyomavirus Promotes Cancer-Associated Fibroblast-Like Phenotype and Cell Invasiveness.

Vaclav Janovec, Boris Ryabchenko, Aneta Škarková, Karolína Pokorná, Daniel Rösel, Jan Brábek, Jan Weber, Jitka Forstová, Ivan Hirsch, Sandra Huérfano

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. 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

10 authors at 2 institutions in 1 country.

Vaclav JanovecDepartment of Genetics and Microbiology, Faculty of Science, Charles University, BIOCEV, 25150 Vestec, Czech Republic.ORCID 0000-0002-6262-3364
Boris RyabchenkoDepartment of Genetics and Microbiology, Faculty of Science, Charles University, BIOCEV, 25150 Vestec, Czech Republic.
Aneta ŠkarkováDepartment of Cell Biology, Faculty of Science, Charles University, BIOCEV, 25150 Vestec, Czech Republic.ORCID 0000-0002-9255-8268
Karolína PokornáIOCB Gilead Research Center, Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, 16000 Prague, Czech Republic.ORCID 0000-0001-7185-9494
Daniel RöselDepartment of Cell Biology, Faculty of Science, Charles University, BIOCEV, 25150 Vestec, Czech Republic.
Jan BrábekDepartment of Cell Biology, Faculty of Science, Charles University, BIOCEV, 25150 Vestec, Czech Republic.ORCID 0000-0001-7754-7299
Jan WeberIOCB Gilead Research Center, Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, 16000 Prague, Czech Republic.ORCID 0000-0002-2799-7352
Jitka ForstováDepartment of Genetics and Microbiology, Faculty of Science, Charles University, BIOCEV, 25150 Vestec, Czech Republic.
Ivan HirschDepartment of Genetics and Microbiology, Faculty of Science, Charles University, BIOCEV, 25150 Vestec, Czech Republic.ORCID 0000-0003-1701-1438
Sandra HuérfanoDepartment of Genetics and Microbiology, Faculty of Science, Charles University, BIOCEV, 25150 Vestec, Czech Republic.ORCID 0000-0001-5221-3014
Charles University · CZCzech Academy of Sciences, Institute of Organic Chemistry and Biochemistry · CZ

Funding

GAUK https://cuni.cz/UKEN-753.html 644217Grantová Agentura České Republiky 19-14445S
6 · The paper itself

Abstract

The tumorigenic potential of mouse polyomavirus (MPyV) has been studied for decades in cell culture models and has been mainly attributed to nonstructural middle T antigen (MT), which acts as a scaffold signal adaptor, activates Src tyrosine kinases, and possesses transforming ability. We hypothesized that MPyV could also transform mouse cells independent of MT via a Toll-like receptor 4 (TLR4)-mediated inflammatory mechanism. To this end, we investigated the interaction of MPyV with TLR4 in mouse embryonic fibroblasts (MEFs) and 3T6 cells, resulting in secretion of interleukin 6 (IL-6), independent of active viral replication. TLR4 colocalized with MPyV capsid protein VP1 in MEFs. Neither TLR4 activation nor recombinant IL-6 inhibited MPyV replication in MEFs and 3T6 cells. MPyV induced STAT3 phosphorylation through both direct and MT-dependent and indirect and TLR4/IL-6-dependent mechanisms. We demonstrate that uninfected mouse fibroblasts exposed to the cytokine environment from MPyV-infected fibroblasts upregulated the expressions of MCP-1, CCL-5, and α-SMA. Moreover, the cytokine microenvironment increased the invasiveness of MEFs and CT26 carcinoma cells. Collectively, TLR4 recognition of MPyV induces a cytokine environment that promotes the cancer-associated fibroblast (CAF)-like phenotype in noninfected fibroblasts and increases cell invasiveness.

Indexed as

CAFIL-6mouse fibroblastsmouse polyomavirusMPyVspheroid invasivenessTLR4

Identifiers

PMID33923020
PMCPMC8123340
OpenAlexW3158502974

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.