Evidence map›Paper›PMID 32372139›Full record

ArticleCancer immunology, immunotherapy : CII2020

Cysteine cathepsins L and X differentially modulate interactions between myeloid-derived suppressor cells and tumor cells.

Tanja Jakoš, Anja Pišlar, Urša Pečar Fonović, Urban Švajger, Janko Kos

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Tanja JakošDepartment of Pharmaceutical Biology, Faculty of Pharmacy, University of Ljubljana, Aškerčeva cesta 7, 1000, Ljubljana, Slovenia.
Anja PišlarDepartment of Pharmaceutical Biology, Faculty of Pharmacy, University of Ljubljana, Aškerčeva cesta 7, 1000, Ljubljana, Slovenia.
Urša Pečar FonovićDepartment of Pharmaceutical Biology, Faculty of Pharmacy, University of Ljubljana, Aškerčeva cesta 7, 1000, Ljubljana, Slovenia.
Urban ŠvajgerDepartment for Therapeutic Services, Blood Transfusion Centre of Slovenia, Ljubljana, Slovenia.
Janko KosDepartment of Pharmaceutical Biology, Faculty of Pharmacy, University of Ljubljana, Aškerčeva cesta 7, 1000, Ljubljana, Slovenia. janko.kos@ffa.uni-lj.si.ORCID http://orcid.org/0000-0002-4228-3518
University of Ljubljana · SIBlood Transfusion Centre of Slovenia · SI

Funding

Javna Agencija za Raziskovalno Dejavnost RS J4-1776Javna Agencija za Raziskovalno Dejavnost RS J4-6811Javna Agencija za Raziskovalno Dejavnost RS J4-8227Javna Agencija za Raziskovalno Dejavnost RS P4-0127
6 · The paper itself

Abstract

Increased proteolytic activity of cysteine cathepsins has long been known to facilitate malignant progression, and it has also been associated with tumor-promoting roles of myeloid-derived suppressor cells (MDSCs). Consequently, cysteine cathepsins have gained much attention as potential targets for cancer therapies. However, cross-talk between tumor cells and MDSCs needs to be taken into account when studying the efficacy of cathepsin inhibitors as anti-cancer agents. Here, we demonstrate the potential of the MDA-MB-231 breast cancer cell line to generate functional MDSCs from CD14

Indexed as

Cathepsin LCD8-Positive T-LymphocytesCell Line, TumorCysteineHumansLeukocytes, MononuclearMyeloid-Derived Suppressor CellsNeoplasm InvasivenessNeoplasmsPC-3 CellsCathepsin LCysteineCancerCathepsin inhibitionCysteine cathepsinsImmunosuppressionMDA-MB-231 cellsMyeloid-derived suppressor cells

Identifiers

PMID32372139
PMCPMC11027625
OpenAlexW3023078240

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.