Evidence map›Paper›PMID 29900042›Full record

ArticleOncoimmunology

Unveiling a CD70-positive subset of cancer-associated fibroblasts marked by pro-migratory activity and thriving regulatory T cell accumulation.

Julie Jacobs, Vanessa Deschoolmeester, Karen Zwaenepoel, Tal Flieswasser, Christophe Deben, Jolien Van den Bossche, Christophe Hermans, Christian Rolfo, Marc Peeters, Olivier De Wever and 4 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 23% 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

48 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 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

14 authors at 3 institutions in 1 country.

Julie JacobsCenter for Oncological Research (CORE), University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.ORCID 0000-0003-2873-3364
Vanessa DeschoolmeesterCenter for Oncological Research (CORE), University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.
Karen ZwaenepoelCenter for Oncological Research (CORE), University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.ORCID 0000-0001-9122-0639
Tal FlieswasserCenter for Oncological Research (CORE), University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.
Christophe DebenCenter for Oncological Research (CORE), University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.ORCID 0000-0001-8085-2040
Jolien Van den BosscheCenter for Oncological Research (CORE), University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.ORCID 0000-0002-2993-024X
Christophe HermansCenter for Oncological Research (CORE), University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.
Christian RolfoCenter for Oncological Research (CORE), University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.ORCID 0000-0002-5109-0267
Marc PeetersCenter for Oncological Research (CORE), University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.ORCID 0000-0003-4969-2303
Olivier De WeverLaboratory of Experimental Cancer Research, Department of Radiation Oncology and Experimental Cancer Research, De Pintelaan 185, Ghent University Hospital, Ghent, Belgium.
Filip LardonCenter for Oncological Research (CORE), University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.
Vasiliki SiozopoulouDepartment of Pathology, Antwerp University Hospital, Wilrijkstraat 10, Edegem, Belgium.
Evelien SmitsCenter for Oncological Research (CORE), University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.ORCID 0000-0001-9255-3435
Patrick PauwelsCenter for Oncological Research (CORE), University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.
University of Antwerp · BEAntwerp University Hospital · BEGhent University Hospital · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer-associated fibroblasts (CAFs) are involved in the proliferative and invasive behavior of colorectal cancer (CRC). Nonetheless, CAFs represent a heterogeneous population with both cancer-promoting and cancer-restraining actions, lacking specific markers to target them. Expression of the immune checkpoint molecule CD70 is normally limited to cells of the lymphoid lineage. Instead, tumor cells hijack CD70 to facilitate immune evasion by increasing the amount of suppressive regulatory T cells (Tregs). The aim of this study was to explore CD70 expression patterns in CRC, not merely focusing on the tumor cells, but also taking the tumor stromal cells into account. We have analyzed the prognostic value of CD70 expression by immunohistochemistry in CRC specimens and its relationship with well-known fibroblast markers and Tregs. In addition,

Indexed as

biomarkerCancer-associated fibroblastsCD70colorectal cancerimmunotherapymigrationprognosisregulatory T cellstumor microenvironment

Identifiers

PMID29900042
PMCPMC5993499
OpenAlexW2791017778

What OpenQuestion holds

Textmetadata
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.