Evidence map›Paper›PMID 35883559›Full record

ArticleBiomolecules2022

Kallikrein-Related Peptidase 6 (KLK6) as a Contributor toward an Aggressive Cancer Cell Phenotype: A Potential Role in Colon Cancer Peritoneal Metastasis.

Hayet Bouzid, Feryel Soualmia, Katerina Oikonomopoulou, Antoninus Soosaipillai, Francine Walker, Khaoula Louati, Rea Lo Dico, Marc Pocard, Chahrazade El Amri, Natalia A Ignatenko and 1 more

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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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

11 authors at 6 institutions in 3 countries.

Hayet BouzidInstitut National de la Santé et de la Recherche Médicale (INSERM) INSERM-1275, Hôpital Lariboisière, 75010 Paris, France.
Feryel SoualmiaSorbonne Université, IBPS, UMR 8256 CNRS-UPMC, ERL INSERM U1164, Biological Adaptation and Ageing, 75005 Paris, France.ORCID 0000-0003-1818-703X
Katerina OikonomopoulouSchroeder Arthritis Institute, Krembil Research Institute, University Health Network, Toronto, ON M5T 3L9, Canada.
Antoninus SoosaipillaiDepartment of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, ON M5T 3L9, Canada.
Francine WalkerDepartment of Pathology, Hôpital Bichat-Claude Bernard, 75018 Paris, France.
Khaoula LouatiInstitut National de la Santé et de la Recherche Médicale (INSERM) INSERM-1275, Hôpital Lariboisière, 75010 Paris, France.
Rea Lo DicoInstitut National de la Santé et de la Recherche Médicale (INSERM) INSERM-1275, Hôpital Lariboisière, 75010 Paris, France.
Marc PocardInstitut National de la Santé et de la Recherche Médicale (INSERM) INSERM-1275, Hôpital Lariboisière, 75010 Paris, France.
Chahrazade El AmriSorbonne Université, IBPS, UMR 8256 CNRS-UPMC, ERL INSERM U1164, Biological Adaptation and Ageing, 75005 Paris, France.ORCID 0000-0002-1028-5113
Natalia A IgnatenkoUniversity of Arizona Cancer Center, University of Arizona, Tucson, AZ 85724, USA.
Dalila DarmoulInstitut National de la Santé et de la Recherche Médicale (INSERM) INSERM-1275, Hôpital Lariboisière, 75010 Paris, France.
Inserm · FRCentre National de la Recherche Scientifique · FRMount Sinai Hospital · CAUniversité Claude Bernard Lyon 1 · FRUniversity Health Network · CAUniversity of Arizona · US

Funding

Role of Kallikrein 6 expression and secretion in colon cancerR01CA157595 · NCI · UNIVERSITY OF ARIZONA · PI IGNATENKO, NATALIA A · 2012 to 2016
$1.7M
National Cancer Institute of the National Institutes of Health R01CA157595NCI NIH HHS R01 CA157595
6 · The paper itself

Abstract

Kallikrein-related peptidases (KLKs) are implicated in many cancer-related processes. KLK6, one of the 15 KLK family members, is a promising biomarker for diagnosis of many cancers and has been associated with poor prognosis of colorectal cancer (CRC) patients. Herein, we evaluated the expression and cellular functions of KLK6 in colon cancer-derived cell lines and in clinical samples from CRC patients. We showed that, although many KLKs transcripts are upregulated in colon cancer-derived cell lines, KLK6, KLK10, and KLK11 are the most highly secreted proteins. KLK6 induced calcium flux in HT29 cells by activation and internalization of protease-activated receptor 2 (PAR2). Furthermore, KLK6 induced extracellular signal-regulated kinases 1 and 2 (ERK1/2) phosphorylation. KLK6 suppression in HCT-116 colon cancer cells decreased the colony formation, increased cell adhesion to extracellular matrix proteins, and reduced spheroid formation and compaction. Immunohistochemistry (IHC) analysis demonstrated ectopic expression of KLK6 in human colon adenocarcinomas but not in normal epithelia. Importantly, high levels of KLK6 protein were detected in the ascites of CRC patients with peritoneal metastasis, but not in benign ascites. These data indicate that KLK6 overexpression is associated with aggressive CRC, and may be applied to differentiate between benign and malignant ascites.

Indexed as

Colonic NeoplasmsPeritoneal NeoplasmsRectal NeoplasmsAscitesHumansKallikreinsPhenotypeKallikreinsKLK6 protein, humancolorectal cancerextracellular matrixkallikrein-related peptidase 6metastasisprotease-activated receptorssignaling

Identifiers

PMID35883559
PMCPMC9312869
OpenAlexW4286224229

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.