Evidence map›Paper›PMID 26395996›Full record

ReviewArchivum immunologiae et therapiae experimentalis2016

The Role of Cathelicidin LL-37 in Cancer Development.

Ewelina Piktel, Katarzyna Niemirowicz, Urszula Wnorowska, Marzena Wątek, Tomasz Wollny, Katarzyna Głuszek, Stanisław Góźdź, Ilya Levental, Robert Bucki

Open access · hybridAbstract readReview
In one paragraph

Review in Archivum immunologiae et therapiae experimentalis, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

58 citing papers in PubMed, 112 citations in OpenAlex.

  1. Review
  2. Endogenous cathelicidin protects againstInfection and immunity · 2026
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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

9 authors at 4 institutions in 2 countries.

Ewelina PiktelDepartment of Microbiological and Nanobiomedical Engineering, Medical University of Białystok, Mickiewicza 2c, 15-222, Białystok, Poland.
Katarzyna NiemirowiczDepartment of Microbiological and Nanobiomedical Engineering, Medical University of Białystok, Mickiewicza 2c, 15-222, Białystok, Poland.
Urszula WnorowskaDepartment of Microbiological and Nanobiomedical Engineering, Medical University of Białystok, Mickiewicza 2c, 15-222, Białystok, Poland.
Marzena WątekHoly Cross Oncology Center of Kielce, Kielce, Poland.
Tomasz WollnyHoly Cross Oncology Center of Kielce, Kielce, Poland.
Katarzyna GłuszekHoly Cross Oncology Center of Kielce, Kielce, Poland.
Stanisław GóźdźThe Faculty of Health Sciences of The Jan Kochanowski University in Kielce, Kielce, Poland.
Ilya LeventalDepartment of Integrative Biology and Pharmacology, The University of Texas Medical School, Houston, TX, USA.
Robert BuckiDepartment of Microbiological and Nanobiomedical Engineering, Medical University of Białystok, Mickiewicza 2c, 15-222, Białystok, Poland. buckirobert@gmail.com.
Medical University of Białystok · PLHoly Cross University · PLJan Kochanowski University · PLThe University of Texas at Austin · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

LL-37 is a C-terminal peptide proteolytically released from 18 kDa human cathelicidin protein (hCAP18). Chronic infections, inflammation, tissue injury and tissue regeneration are all linked with neoplastic growth, and involve LL-37 antibacterial and immunomodulatory functions. Such a link points to the possible involvement of LL-37 peptide in carcinogenesis. An increasing amount of evidence suggests that LL-37 can have two different and contradictory effects--promotion or inhibition of tumor growth. The mechanisms are tissue-specific, complex, and depend mostly on the ability of LL-37 to act as a ligand for different membrane receptors whose expression varies on different cancer cells. Overexpression of LL-37 was found to promote development and progression of ovarian, lung and breast cancers, and to suppress tumorigenesis in colon and gastric cancer. This review explores and summarizes the current views on how LL-37 contributes to immunity, pathophysiology and cell signaling involved in malignant tumor growth.

Indexed as

CarcinogenesisImmunity, InnateAnimalsAntimicrobial Cationic PeptidesCathelicidinsCell Growth ProcessesGene Expression Regulation, NeoplasticHumansImmunomodulationOrgan SpecificitySignal TransductionAntimicrobial Cationic PeptidesCathelicidinsCancerCarcinogenesisCathelicidinImmune systemLL-37

Identifiers

PMID26395996
PMCPMC4713713
OpenAlexW1853873243

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.