Evidence map›Paper›PMID 35008289›Full record

ArticleCancers2021

A Chemerin Peptide Analog Stimulates Tumor Growth in Two Xenograft Mouse Models of Human Colorectal Carcinoma.

Justa Friebus-Kardash, Petra Schulz, Sandy Reinicke, Cordula Karthaus, Quirino Schefer, Sebastian Bandholtz, Carsten Grötzinger

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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 42% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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  4. Review
  5. Review
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 2 institutions in 1 country.

Justa Friebus-KardashDepartment of Hepatology and Gastroenterology, Charité-University Medicine Berlin, Corporate Member of Free University Berlin and Humboldt University Berlin, 13353 Berlin, Germany.ORCID 0000-0002-6747-1240
Petra SchulzDepartment of Hepatology and Gastroenterology, Charité-University Medicine Berlin, Corporate Member of Free University Berlin and Humboldt University Berlin, 13353 Berlin, Germany.
Sandy ReinickeDepartment of Hepatology and Gastroenterology, Charité-University Medicine Berlin, Corporate Member of Free University Berlin and Humboldt University Berlin, 13353 Berlin, Germany.
Cordula KarthausDepartment of Hepatology and Gastroenterology, Charité-University Medicine Berlin, Corporate Member of Free University Berlin and Humboldt University Berlin, 13353 Berlin, Germany.
Quirino ScheferDepartment of Hepatology and Gastroenterology, Charité-University Medicine Berlin, Corporate Member of Free University Berlin and Humboldt University Berlin, 13353 Berlin, Germany.
Sebastian BandholtzDepartment of Hepatology and Gastroenterology, Charité-University Medicine Berlin, Corporate Member of Free University Berlin and Humboldt University Berlin, 13353 Berlin, Germany.
Carsten GrötzingerDepartment of Hepatology and Gastroenterology, Charité-University Medicine Berlin, Corporate Member of Free University Berlin and Humboldt University Berlin, 13353 Berlin, Germany.ORCID 0000-0001-9872-3087
Humboldt-Universität zu Berlin · DEGerman Cancer Research Center · DE

Funding

Federal Ministry of Education and Research IP614Federal Ministry of Education and Research IPT614A
6 · The paper itself

Abstract

backgroundChemerin plasma concentration has been reported to be positively correlated with the risk of colorectal cancer. However, the potential regulation of CRC tumorigenesis and progression has not yet been investigated in an experimental setting. This study addresses this hypothesis by investigating proliferation, colony formation, and migration of CRC cell lines in vitro as well as in animal models.

methodsIn vitro, microscopic assays to study proliferation, as well as a scratch-wound assay for migration monitoring, were applied using the human CRC cell lines HCT116, HT29, and SW620 under the influence of the chemerin analog CG34. The animal study investigated HCT116-luc and HT29-luc subcutaneous tumor size and bioluminescence during treatment with CG34 versus control, followed by an ex-vivo analysis of vessel density and mitotic activity.

resultsWhile the proliferation of the three CRC cell lines in monolayers was not clearly stimulated by CG34, the chemerin analog promoted colony formation in three-dimensional aggregates. An effect on cell migration was not observed. In the treatment study, CG34 significantly stimulated both growth and bioluminescence signals of HCT116-luc and HT29-luc xenografts.

conclusionsThe results of this study represent the first indication of a tumor growth-stimulating effect of chemerin signaling in CRC.

Indexed as

CCLR2CG34chemerinCMKLR1colorectal cancerGPR1peptide analogtumor treatmentxenograft mouse model

Identifiers

PMID35008289
PMCPMC8750290
OpenAlexW4225901341

What OpenQuestion holds

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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.