Evidence map›Paper›PMID 30261624›Full record

ArticleMolecules (Basel, Switzerland)2018

Anticancer and Differentiation Properties of the Nitric Oxide Derivative of Lopinavir in Human Glioblastoma Cells.

Maria Sofia Basile, Emanuela Mazzon, Tamara Krajnovic, Dijana Draca, Eugenio Cavalli, Yousef Al-Abed, Placido Bramanti, Ferdinando Nicoletti, Sanja Mijatovic, Danijela Maksimovic-Ivanic

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
4.1field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Antiretroviral Drugs Impact Autophagy: Opportunities for Drug Repurposing.Frontiers in bioscience (Landmark edition) · 2024
    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

10 authors at 4 institutions in 3 countries.

Maria Sofia BasileDepartment of Immunology, Institute for Biological Research "Sinisa Stankovic", Belgrade University, Bulevar despota Stefana 142, 11060 Belgrade, Serbia. sofiabasile@hotmail.it.
Emanuela MazzonIRCCS Centro Neurolesi Bonino Pulejo, Strada Statale 113, C.da Casazza, 98124 Messina, Italy. emanuela.mazzon@irccsme.it.
Tamara KrajnovicDepartment of Immunology, Institute for Biological Research "Sinisa Stankovic", Belgrade University, Bulevar despota Stefana 142, 11060 Belgrade, Serbia. tamara_krajnovic@yahoo.com.
Dijana DracaDepartment of Immunology, Institute for Biological Research "Sinisa Stankovic", Belgrade University, Bulevar despota Stefana 142, 11060 Belgrade, Serbia. dracadiana@gmail.com.
Eugenio CavalliIRCCS Centro Neurolesi Bonino Pulejo, Strada Statale 113, C.da Casazza, 98124 Messina, Italy. eugeniocavalli9@hotmail.it.
Yousef Al-AbedCenter for Molecular Innovation, The Feinstein Institute for Medical Research, 350 Community drive, Manhasset, NY 11030, USA. yalabed@northwell.edu.
Placido BramantiIRCCS Centro Neurolesi Bonino Pulejo, Strada Statale 113, C.da Casazza, 98124 Messina, Italy. placido.bramanti@irccsme.it.
Ferdinando NicolettiDepartment of Biomedical and Biotechnological Sciences, University of Catania, Via S. Sofia 89, 95123 Catania, Italy. ferdinic@unict.it.
Sanja MijatovicDepartment of Immunology, Institute for Biological Research "Sinisa Stankovic", Belgrade University, Bulevar despota Stefana 142, 11060 Belgrade, Serbia. sanjamama@ibiss.bg.ac.rs.
Danijela Maksimovic-IvanicDepartment of Immunology, Institute for Biological Research "Sinisa Stankovic", Belgrade University, Bulevar despota Stefana 142, 11060 Belgrade, Serbia. nelamax@ibiss.bg.ac.rs.
University of Belgrade · RSCentro Neurolesi Bonino Pulejo · ITUniversity of Catania · ITFeinstein Institute for Medical Research · US

Funding

IRCCS "Centro Neurolesi Bonino Pulejo", Messina-Italy;Ministry of Education, Science and Technological Development of the Republic of Serbia current research funds 2016; project No. 173013
6 · The paper itself

Abstract

Glioblastoma (GBM) is the most frequent and deadly form of primary malignant brain tumor among adults. A promising emerging approach for GBM treatment may be offered from HIV protease inhibitors (HIV-PIs). In fact, in addition to their primary pharmacological activity in the treatment of HIV infection, they possess important anti-neoplastic effects. According to previous studies, the addition of a nitric oxide (NO) donating group to parental compounds can reduce their toxicity and enhance the anticancer action of various compounds, including HIV-PIs. In this study we compared the effects of the HIV-PI Lopinavir (Lopi) and of its NO-derivative Lopinavir-NO (Lopi-NO) on the in vitro growth of LN-229 and U-251 human GBM cell lines. Lopi-NO reduced the viability of LN-229 and U-251 cells at significantly lower concentrations than the parental drug. In particular, Lopi-NO inhibited tumor cell proliferation and induced the differentiation of U-251 cells toward an astrocyte-like phenotype without triggering significant cell death in both cell types. The anticancer effect of Lopi-NO was persistent even upon drug removal. Furthermore, Lopi-NO induced strong autophagy that did not appear to be related to its chemotherapeutic action. Overall, our results suggest that Lopi-NO could be a potential effective anticancer drug for GBM treatment.

Indexed as

ApoptosisCell DifferentiationCell ProliferationGlioblastomaHIV Protease InhibitorsHumansLopinavirNitric OxideTumor Cells, CulturedHIV Protease InhibitorsLopinavirNitric OxideglioblastomaHIV protease inhibitorsLopinavirLopinavir-NOnitric oxide

Identifiers

PMID30261624
PMCPMC6222694
OpenAlexW2892933845

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.