Evidence map›Paper›PMID 26304506›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

Distinctive expression pattern of interleukin-17 cytokine family members in colorectal cancer.

Ahmed Al-Samadi, Shirin Moossavi, Abdelhakim Salem, Masoud Sotoudeh, Sarianna M Tuovinen, Yrjö T Konttinen, Tuula Salo, Faraz Bishehsari

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Observational
  12. Targeting the interleukin-17 immune axis for cancer immunotherapy.The Journal of experimental medicine · 2020
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. 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

8 authors at 5 institutions in 3 countries.

Ahmed Al-SamadiDepartment of Medicine, Institute of Clinical Medicine, University of Helsinki, Helsinki, Finland.
Shirin MoossaviDigestive Oncology Research Center; Digestive Disease Research Institute, Tehran University of Medical Sciences, Shariati Hospital, North Amirabad Ave., Tehran, 14117, Iran. shirin.moossavi@gmail.com.
Abdelhakim SalemDepartment of Medicine, Institute of Clinical Medicine, University of Helsinki, Helsinki, Finland.
Masoud SotoudehPathology Department, Tehran University of Medical Sciences, Tehran, Iran.
Sarianna M TuovinenDepartment of Medicine, Institute of Clinical Medicine, University of Helsinki, Helsinki, Finland.
Yrjö T KonttinenDepartment of Medicine, Institute of Clinical Medicine, University of Helsinki, Helsinki, Finland.
Tuula SaloDepartment of Oral and Maxillofacial Diseases, University of Helsinki, Helsinki, Finland.
Faraz BishehsariDivision of Digestive Diseases, Rush University Medical Center, Chicago, IL, USA.
University of Helsinki · FIInvalidisäätiö · FIRush University Medical Center · USShariati Hospital · IRTehran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is one of the most common cancers in both genders. Even though interleukin (IL)-17A was shown to play an important role in intestinal tumourigenesis and CRC, other IL-17 family members were not studied well. We therefore studied the expression of IL-17 cytokine family members in CRC. Ten healthy colons and ten CRC mucosa were immunostained for IL-17B, IL-17C, IL-17E, and IL-17F, and their receptors IL-17RA, IL-17RB, and IL-17RC. Double immunofluorescence staining of the CRC mucosa was done for IL-17B with markers of neutrophils, endothelial cells, macrophages, T cells, mast cells, or fibroblasts. While IL-17B was increased in CRC with a strong presence both in the epithelial and stromal compartments, IL-17C showed different expression depending on the grade of differentiation and IL-17E remained unchanged. In contrast, IL-17F was decreased in CRC compared to healthy control. Colon epithelial cells stained positive for IL-17RA, IL-17RB, and IL-17RC in both healthy control and CRC. Neutrophils were the main source of IL-17B in the stroma. IL-17 family members demonstrated distinct expression patterns in CRC, suggesting a differential role exerted by each member in colon carcinogenesis.

Indexed as

AdenocarcinomaColorectal NeoplasmsHumansImmunohistochemistryInterleukin-17Intestinal MucosaInterleukin-17Colorectal cancerIL-17IL-17BNeutrophil

Identifiers

PMID26304506
OpenAlexW1166521652

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.