Evidence map›Paper›PMID 28759013›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2017

Papillary renal cell carcinoma-derived chemerin, IL-8, and CXCL16 promote monocyte recruitment and differentiation into foam-cell macrophages.

Krzysztof M Krawczyk, Helén Nilsson, Roni Allaoui, David Lindgren, Michael Arvidsson, Karin Leandersson, Martin E Johansson

Open access · hybridAbstract read
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

24 citing papers in PubMed, 46 citations in OpenAlex.

  1. Interleukin-8 in health and disease.Molecular biomedicine · 2026
    Review
  2. Current issues in molecular biology · 2026
    Article
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  18. The Role of CXCL16 in the Pathogenesis of Cancer and Other Diseases.International journal of molecular sciences · 2021
    Review
  19. Review
  20. 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

7 authors at 1 institution in 1 country.

Krzysztof M KrawczykDepartment of Translational Medicine, Center for Molecular Pathology, Lund University, Malmö, Sweden.
Helén NilssonDepartment of Translational Medicine, Center for Molecular Pathology, Lund University, Malmö, Sweden.
Roni AllaouiDepartment of Translational Medicine, Cancer Immunology, Lund University, Malmö, Sweden.
David LindgrenDepartment of Laboratory Medicine, Translational Cancer Research, Lund University, Lund, Sweden.
Michael ArvidssonDepartment of Translational Medicine, Center for Molecular Pathology, Lund University, Malmö, Sweden.
Karin LeanderssonDepartment of Translational Medicine, Cancer Immunology, Lund University, Malmö, Sweden.
Martin E JohanssonDepartment of Translational Medicine, Center for Molecular Pathology, Lund University, Malmö, Sweden.
Lund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Papillary renal cell carcinoma (pRCC) is the second most common type of renal cell carcinoma. The only curative treatment available for pRCC is radical surgery. If the disease becomes widespread, neither chemo- nor radiotherapy will have therapeutic effect, hence further research on pRCC is of utmost importance. Histologically, pRCC is characterized by a papillary growth pattern with focal aggregation of macrophages of the foam cell phenotype. In other forms of cancer, a clear role for tumor-associated macrophages during cancer growth and progression has been shown. Although the presence of foamy macrophages is a histological hallmark of pRCC tumors, little is known regarding their role in pRCC biology. In order to study the interaction between pRCC tumor and myeloid cells, we established primary cultures from pRCC tissue. We show that human pRCC cells secrete the chemokines IL-8, CXCL16, and chemerin, and that these factors attract primary human monocytes in vitro. RNAseq data from The Cancer Genome Atlas confirmed a high expression of these factors in pRCC tissue. Conditioned medium from pRCC cultures induced a shift in human monocytes toward the M2 macrophage phenotype. In extended cultures, these macrophages became enlarged and loaded with lipids, adopting the foam cell morphology found in pRCC tissue. These results show for the first time that pRCC primary tumor cells secrete factors that attract and differentiate monocytes into anti-inflammatory tumor-associated macrophages with foam cell histology.

Indexed as

AgedCarcinoma, Renal CellCells, CulturedCell TransdifferentiationChemokine CXCL16ChemokinesChemokines, CXCChemotaxis, LeukocyteCoculture TechniquesCulture Media, ConditionedFoam CellsHumansIntercellular Signaling Peptides and ProteinsInterleukin-8Kidney NeoplasmsMaleChemokine CXCL16ChemokinesChemokines, CXCCulture Media, ConditionedCXCL16 protein, humanCXCL8 protein, humanIntercellular Signaling Peptides and ProteinsInterleukin-8Neoplasm ProteinsRARRES2 protein, humanReceptors, Scavenger

Identifiers

PMID28759013
PMCPMC5668481
OpenAlexW2741350201

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.