Evidence map›Paper›PMID 25848918›Full record

ArticleOncotarget2015

Nitroxoline impairs tumor progression in vitro and in vivo by regulating cathepsin B activity.

Bojana Mirković, Boštjan Markelc, Miha Butinar, Ana Mitrović, Izidor Sosič, Stanislav Gobec, Olga Vasiljeva, Boris Turk, Maja Čemažar, Gregor Serša and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

29 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
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  8. Frontiers in pharmacology · 2022
    Article
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  11. Review
  12. Article
  13. Cells · 2020
    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 3 institutions in 1 country.

Bojana MirkovićFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
Boštjan MarkelcDepartment of Experimental Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Miha ButinarDepartment of Biochemistry and Molecular and Structural Biology, Jožef Stefan Institute, Ljubljana, Slovenia.
Ana MitrovićFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
Izidor SosičFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
Stanislav GobecFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
Olga VasiljevaDepartment of Biochemistry and Molecular and Structural Biology, Jožef Stefan Institute, Ljubljana, Slovenia.
Boris TurkDepartment of Biochemistry and Molecular and Structural Biology, Jožef Stefan Institute, Ljubljana, Slovenia.
Maja ČemažarDepartment of Experimental Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Gregor SeršaDepartment of Experimental Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Janko KosFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
University of Ljubljana · SIInstitute of Oncology Ljubljana · SIJožef Stefan Institute · SI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cathepsin B is a ubiquitously expressed lysosomal cysteine protease that participates in protein turnover within lysosomes. However, its protein and activity levels have been shown to be increased in cancer. Cathepsin B endopeptidase activity is involved in the degradation of extracellular matrix, a process that promotes tumor invasion, metastasis and angiogenesis. Previously, we reported an established antibiotic nitroxoline as a potent and selective inhibitor of cathepsin B. In the present study, we elucidated its anti-tumor properties in in vitro and in vivo tumor models. Tumor and endothelial cell lines with high levels of active cathepsin B were selected for functional analysis of nitroxoline in vitro. Nitroxoline significantly reduced extracellular DQ-collagen IV degradation by all evaluated cancer cell lines using spectrofluorimetry. Nitroxoline also markedly decreased tumor cell invasion monitored in real time and reduced the invasive growth of multicellular tumor spheroids, used as a 3D in vitro model of tumor invasion. Additionally, endothelial tube formation was significantly reduced by nitroxoline in an in vitro angiogenesis assay. Finally, nitroxoline significantly abrogated tumor growth, angiogenesis and metastasis in vivo in LPB fibrosarcoma and MMTV-PyMT breast cancer mouse models. Overall, our results designate nitroxoline as a promising drug candidate for anti-cancer treatment.

Indexed as

Angiogenesis Inducing AgentsAnimalsCase-Control StudiesCathepsin BCell Growth ProcessesCell Line, TumorDisease ProgressionEndothelial CellsFemaleFibrosarcomaHumansHuman Umbilical Vein Endothelial CellsMiceMice, Inbred C57BLMice, TransgenicNeoplasm MetastasisAngiogenesis Inducing AgentsCathepsin BNitroquinolinesnitroxolineangiogenesiscathepsin Bmetastasisnitroxolinetumor invasion

Identifiers

PMID25848918
PMCPMC4662473
OpenAlexW1826848231

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.