Evidence map›Paper›PMID 26960691›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

Oligoesculin fraction induces anti-tumor effects and promotes immune responses on B16-F10 mice melanoma.

Imen Mokdad Bzeouich, Nadia Mustapha, Aicha Sassi, Kamel Ghedira, Mohamed Ghoul, Latifa Chebil, José Luis, Leila Chekir-Ghedira

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. The role of nitric oxide in melanoma.Biochimica et biophysica acta. Reviews on cancer · 2017
    Review
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

8 authors at 3 institutions in 2 countries.

Imen Mokdad BzeouichLaboratory of Cellular and Molecular Biology. Faculty of Dental Medicine, University of Monastir, Avicenne Street 5000, Monastir, Tunisia.
Nadia MustaphaLaboratory of Cellular and Molecular Biology. Faculty of Dental Medicine, University of Monastir, Avicenne Street 5000, Monastir, Tunisia.
Aicha SassiLaboratory of Cellular and Molecular Biology. Faculty of Dental Medicine, University of Monastir, Avicenne Street 5000, Monastir, Tunisia.
Kamel GhediraUnit of Bioactive and Natural Substances and Biotechnology UR12ES12. Faculty of Pharmacy, University of Monastir, Avicenne Street 5000, Monastir, Tunisia.
Mohamed GhoulLaboratory of Biomolecular Engineering, National School of Agronomy and Food Industries, National Polytechnics Institute of Lorraine ENSAIA-INPL, 54505, Vandoeuvre les Nancy, France.
Latifa ChebilLaboratory of Biomolecular Engineering, National School of Agronomy and Food Industries, National Polytechnics Institute of Lorraine ENSAIA-INPL, 54505, Vandoeuvre les Nancy, France.
José LuisINSERM UMR 911-CRO2, Faculty of Pharmacy, Aix-Marseille University, Marseille, France.
Leila Chekir-GhediraLaboratory of Cellular and Molecular Biology. Faculty of Dental Medicine, University of Monastir, Avicenne Street 5000, Monastir, Tunisia. leila.chekir@laposte.net.
University of Monastir · TNÉcole Nationale de la Statistique et de l'Analyse de l'Information · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Laccase was used to enzymatically polymerize esculin. Oligoesculin fraction was obtained after ultrafiltration through a 5-kDa membrane. Several studies have been carried out to prove the effectiveness of natural substances such as immunomodulators to promote the anti-cancer activity in situ. The purpose of our report was to explore whether the anti-tumor potential of the oligoesculin fraction in vitro and in vivo is linked to its immunological mechanisms in melanoma-bearing mice. We revealed that oligoesculin fraction reduced B16-F10 proliferation and migration in vitro in a dose-related manner. Moreover, melanin synthesis and tyrosinase activity were inhibited in these melanoma cells in a concentration-dependent way. The anti-tumor potential of oligoesculin fraction was also assessed in vivo. Our results showed that intraperitoneal administration of oligoesculin fraction, at 50 mg/kg body weight (b.w.) for 21 days, reduced tumor size and weight with percentages of inhibition of 94 and 87 %, respectively. Oligoesculin fraction was effective in promoting lysosomal activity and nitric oxide (NO) production by peritoneal macrophages in tumor-implanted mice. In addition, the activities of natural killer (NK), cytotoxic T lymphocytes, and macrophages were significantly enhanced by oligoesculin fraction. These findings suggested that this polymer with its anti-tumor and immunomodulatory properties could be used for the treatment of melanoma.

Indexed as

AnimalsAntineoplastic AgentsCytotoxicity, ImmunologicEsculinImmunologic FactorsKiller Cells, NaturalMacrophagesMelanoma, ExperimentalMiceMice, Inbred BALB CSkin NeoplasmsT-Lymphocytes, CytotoxicAntineoplastic AgentsEsculinImmunologic FactorsAnti-tumor activityImmunomodulatory effectMelanomaMigrationOligoesculin fraction

Identifiers

PMID26960691
OpenAlexW2295864827

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.