Evidence map›Paper›PMID 28194418›Full record

ArticleBioMed research international2017

Antineoplastic Effects of Honokiol on Melanoma.

Ruth Guillermo-Lagae, Sreevidya Santha, Milton Thomas, Emily Zoelle, Jonathan Stevens, Radhey S Kaushik, Chandradhar Dwivedi

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

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  5. Inhibitory effect of polyphenols (phenolic acids, lignans, and stilbenes) on cancer by regulating signal transduction pathways: a review.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
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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

7 authors at 3 institutions in 1 country.

Ruth Guillermo-LagaeDepartment of Pharmaceutical Sciences, South Dakota State University, Brookings, SD 57007, USA.
Sreevidya SanthaDepartment of Pharmaceutical Sciences, South Dakota State University, Brookings, SD 57007, USA; Department of Pharmacology & Therapeutics, Roswell Park Cancer Institute (RPCI), Buffalo, NY 14263, USA.
Milton ThomasDepartment of Biology and Microbiology; and Department of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, SD 57007, USA.
Emily ZoelleDepartment of Pharmaceutical Sciences, South Dakota State University, Brookings, SD 57007, USA; University of Maryland Baltimore Washington Medical Center, Glen Burnie, MD 21061, USA.
Jonathan StevensDepartment of Pharmaceutical Sciences, South Dakota State University, Brookings, SD 57007, USA.
Radhey S KaushikDepartment of Biology and Microbiology; and Department of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, SD 57007, USA.ORCID 0000-0003-4204-9323
Chandradhar DwivediDepartment of Pharmaceutical Sciences, South Dakota State University, Brookings, SD 57007, USA.ORCID 0000-0003-3478-8660
South Dakota State University · USRoswell Park Comprehensive Cancer Center · USUniversity of Maryland, Baltimore · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Honokiol, a plant lignan has been shown to have antineoplastic effects against nonmelanoma skin cancer developments in mice. In this study, antineoplastic effects of honokiol were investigated in malignant melanoma models. In vitro effects of honokiol treatment on SKMEL-2 and UACC-62 melanoma cells were evaluated by measuring the cell viability, proliferation, apoptosis, cell cycle analysis, and expressions of various proteins associated with cell cycle progression and apoptosis. For the in vivo study, male nude mice inoculated with SKMEL-2 or UACC-62 cells received injections of sesame oil or honokiol for two to seven weeks. In vitro honokiol treatment caused significant decrease in cell viability, proliferation, cell cycle arrest, increased apoptosis, and modulation of apoptotic and cell cycle regulatory proteins. Honokiol caused an accumulation of cells in the G2/M phase of the cell cycle in SKMEL-2 and G0/G1 phase in UACC-62 cells. An elevated level of caspases and PARP were observed in both cell lines treated with honokiol. A decrease in the expression of various cell cycle regulatory proteins was also observed in honokiol treated cells. Honokiol caused a significant reduction of tumor growth in SKMEL-2 and UACC-62 melanoma xenografts. These findings suggest that honokiol is a good candidate for further studies as a possible treatment for malignant melanoma.

Indexed as

Allyl CompoundsAnimalsAntineoplastic Agents, PhytogenicApoptosisBiphenyl CompoundsCell CycleCell Line, TumorCell SurvivalGene Expression Regulation, NeoplasticHumansLignansMaleMelanomaMiceMice, NudeNeoplasm ProteinsAllyl CompoundsAntineoplastic Agents, PhytogenicBiphenyl CompoundshonokiolLignansNeoplasm ProteinsPhenols

Identifiers

PMID28194418
PMCPMC5282456
OpenAlexW2571885982

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.