Evidence map›Paper›PMID 32923147›Full record

ArticleOncoimmunology2020

Systemic inflammation is associated with circulating cell death released keratin 18 fragments in colorectal cancer.

Päivi Sirniö, Juha P Väyrynen, Shivaprakash J Mutt, Karl-Heinz Herzig, Jaroslaw Walkowiak, Kai Klintrup, Jyrki Mäkelä, Tuomo J Karttunen, Markus J Mäkinen, Anne Tuomisto

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Roles of Keratins in Intestine.International journal of molecular sciences · 2022
    Review
  10. Article
  11. 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 4 institutions in 3 countries.

Päivi SirniöCancer and Translational Medicine Research Unit, University of Oulu, Oulu 90014, Finland.
Juha P VäyrynenCancer and Translational Medicine Research Unit, University of Oulu, Oulu 90014, Finland.ORCID 0000-0002-8683-2996
Shivaprakash J MuttResearch Unit of Biomedicine and Biocenter Oulu, Department of Physiology, University of Oulu, Oulu 90014, Finland.
Karl-Heinz HerzigResearch Unit of Biomedicine and Biocenter Oulu, Department of Physiology, University of Oulu, Oulu 90014, Finland.
Jaroslaw WalkowiakDepartment of Gastroenterology and Metabolism, Poznan University of Medical Sciences, Poznan, Poland.
Kai KlintrupDepartment of Pathology, Oulu University Hospital and Medical Research Center Oulu, Oulu 90029, Finland.
Jyrki MäkeläDepartment of Pathology, Oulu University Hospital and Medical Research Center Oulu, Oulu 90029, Finland.
Tuomo J KarttunenCancer and Translational Medicine Research Unit, University of Oulu, Oulu 90014, Finland.
Markus J MäkinenCancer and Translational Medicine Research Unit, University of Oulu, Oulu 90014, Finland.
Anne TuomistoCancer and Translational Medicine Research Unit, University of Oulu, Oulu 90014, Finland.ORCID 0000-0002-9949-1887
Oulu University Hospital · FIPoznan University of Medical Sciences · PLBrigham and Women's Hospital · USUniversity of Oulu · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic inflammation is a stage-independent marker of poor prognosis in colorectal cancer (CRC), activated in a complex, multifactorial process. It has been proposed that one of the main factors driving systemic inflammation may be tumor necrosis. Keratin 18 (KRT18) fragments are released from dead cells and their serum levels are markers for apoptotic and necrotic cell death. In CRC, high KRT18 levels associate with advanced disease, but their relationship with tumor necrosis and systemic inflammation is unknown. In this study, serum total soluble KRT18 (tKRT18) and apoptosis-related, caspase-cleaved fragment (aKRT18) levels were measured preoperatively from 328 CRC patients, and their difference was calculated to assess necrosis related KRT18 (nKRT18) levels. The relationships of these markers with tumor necrosis, clinicopathologic features, systemic inflammation markers (C-reactive protein, albumin, and 13 cytokines), and survival were analyzed. High serum tKRT18, aKRT18, and nKRT18 levels showed association with a higher extent of tumor necrosis, distant metastasis, and increased levels of several markers of systemic inflammation, including CXCL8. High serum tKRT18 (multivariable HR 1.94, 95% CI 1.28-2.95,

Indexed as

Colorectal NeoplasmsKeratin-18Cell DeathFemaleHumansInflammationMalePrognosisKeratin-18Colorectal cancerinflammationkeratin 18necrosissurvival

Identifiers

PMID32923147
PMCPMC7458668
OpenAlexW3037227945

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.