Evidence map›Paper›PMID 32566073›Full record

ArticleOxidative medicine and cellular longevity2020

Zinc Oxide Nanoparticle Synergizes Sorafenib Anticancer Efficacy with Minimizing Its Cytotoxicity.

Ahmed Nabil, Mohamed M Elshemy, Medhat Asem, Marwa Abdel-Motaal, Heba F Gomaa, Faten Zahran, Koichiro Uto, Mitsuhiro Ebara

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 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
2.4field-weighted citation impact, top 12% 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, 43 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

8 authors at 6 institutions in 3 countries.

Ahmed NabilResearch Center for Functional Materials, National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.ORCID https://orcid.org/0000-0002-5617-4726
Mohamed M ElshemyFaculty of Science, Menoufia University, Menoufia, Egypt.
Medhat AsemFaculty of Science, Menoufia University, Menoufia, Egypt.
Marwa Abdel-MotaalDepartment of Chemistry, Faculty of Science, Mansoura University, Mansoura, Egypt.
Heba F GomaaZoology Department, Faculty of Science, Ain-Shams University, Biology Department, Faculty of Sciences and Arts-Scientific Departments, Qassim University, Saudi Arabia.
Faten ZahranBiochemistry Department, Faculty of Science, Zagazig University, Egypt.
Koichiro UtoResearch Center for Functional Materials, National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.
Mitsuhiro EbaraResearch Center for Functional Materials, National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.ORCID https://orcid.org/0000-0002-7906-0350
Menoufia University · EGQassim University · SABeni-Suef University · EGNational Institute for Materials Science · JPUniversity of Tsukuba · JPZagazig University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer, as a group, represents the most important cause of death worldwide. Unfortunately, the available therapeutic approaches of cancer including surgery, chemotherapy, radiotherapy, and immunotherapy are unsatisfactory and represent a great challenge as many patients have cancer recurrence and severe side effects. Methotrexate (MTX) is a well-established (antineoplastic or cytotoxic) chemotherapy and immunosuppressant drug used to treat different types of cancer, but its usage requires high doses causing severe side effects. Therefore, we need a novel drug with high antitumor efficacy in addition to safety. The aim of this study was the evaluation of the antitumor efficacy of zinc oxide nanoparticle (ZnO-NPs) and sorafenib alone or in combination on solid Ehrlich carcinoma (SEC) in mice. Sixty adult female Swiss-albino mice were divided equally into 6 groups as follows: control, SEC, MTX, ZnO-NPs, sorafenib, and ZnO-NPs+sorafenib; all treatments continued for 4 weeks. ZnO-NPs were characterized by TEM, zeta potential, and SEM mapping. Data showed that ZnO-NPs synergized with sorafenib as a combination therapy to execute more effective and safer anticancer activity compared to monotherapy as showed by a significant reduction (

Indexed as

AnimalsAntineoplastic AgentsApoptosisCaspase 3Cell ProliferationCell SurvivalCytochromes cDNADNA FragmentationFemaleMetal NanoparticlesMiceOxidative StressSorafenibTumor BurdenZinc OxideAntineoplastic AgentsCaspase 3Cytochromes cDNASorafenibZinc Oxide

Identifiers

PMID32566073
PMCPMC7275957
OpenAlexW3030932735

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.