Evidence map›Paper›PMID 32458010›Full record

ReviewNaunyn-Schmiedeberg's archives of pharmacology2020

Thymoquinone-chemotherapeutic combinations: new regimen to combat cancer and cancer stem cells.

Ali H El-Far, Mohamed A Tantawy, Soad K Al Jaouni, Shaker A Mousa

Abstract readReview
PubMed Publisher
In one paragraph

Review in Naunyn-Schmiedeberg's archives of pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
7.4field-weighted citation impact, top 3% 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

18 citing papers in PubMed, 40 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

4 authors at 4 institutions in 3 countries.

Ali H El-FarDepartment of Biochemistry, Faculty of Veterinary Medicine, Damanhour University, Damanhour, 22511, Egypt. ali.elfar@damanhour.edu.eg.
Mohamed A TantawyDepartment of Hormones, Medical Research Division, National Research Center, Dokki, Giza, 12622, Egypt. mohamed_tantawy@daad-alumni.de.ORCID 0000-0003-4014-6074
Soad K Al JaouniDepartment of Pediatric Hematology/Oncology, King Abdulaziz University Hospital and Scientific Chair of Yousef Abdul Latif Jameel of Prophetic Medicine Application, Faculty of Medicine, King Abdulaziz University, Jeddah, 21589, Saudi Arabia.
Shaker A MousaPharmaceutical Research Institute, Albany College of Pharmacy and Health Sciences, Rensselaer, NY, 12144, USA.
Albany College of Pharmacy and Health Sciences · USDamanhour University · EGKing Abdulaziz University · SANational Research Centre · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is a worldwide disease that causes millions of cases of mortality and morbidity. The major problem associated with the cancer is its resistance to conventional therapy and a high relapse rate. The use of chemotherapy to treat cancer began at the start of the twentieth century with attempts to control cancer. In time advance, many cancer chemotherapeutic agents have been developed for cancer treatment with different mechanisms of action including the alkylating agents, antimetabolites, antimicrotubule, topoisomerase inhibitors, and cytotoxic antibiotics, all of which have toxic effects toward normal cells in the body. Here, we reviewed chemotherapeutics' anticancer role potentiation and safety by thymoquinone (TQ) alone or in combination with the most common therapeutic drugs. Our search was done through PubMed, Science Direct, Springer Link, Taylor & Francis Online, Wiley Online Library, Nature publication group, SAGE Journals, and Web of Science databases. We recognized that TQ-chemotherapeutics combination increased chemo-modulation to the anticancer effect of different chemotherapeutics and protected the normal body cells from the toxic injuries that are induced by chemotherapeutics based on its antioxidant power. Moreover, the current study investigates the possible combinatory effect of TQ and chemotherapeutics to control cancer stem cells through molecular docking targeting of wingless/integrated (Wnt) and Hedgehog (Hh). We found that TQ modulates the Wnt and Hh pathways, by binding with tankyrase-2 and smoothened 7TM receptor, respectively, more efficiently than most chemotherapeutics drugs, while methotrexate showed high-binding affinity compared with TQ. Therefore, we encourage researchers to investigate the chemo-modulatory potential and protective effects of TQ in combination with chemotherapeutics for either cancer or cancer stem cell treatment.

Indexed as

AnimalsAntineoplastic Combined Chemotherapy ProtocolsBenzoquinonesHedgehog ProteinsHumansMolecular Docking SimulationNeoplasmsNeoplastic Stem CellsProtein Interaction Domains and MotifsSmoothened ReceptorTankyrasesWnt ProteinsWnt Signaling PathwayBenzoquinonesHedgehog ProteinsSmoothened ReceptorSMO protein, humanTankyrasesthymoquinoneTNKS2 protein, humanWnt ProteinsAnticancer potentialCancer stem cellsChemotherapeutic safetyMolecular dockingThymoquinone

Identifiers

PMID32458010
OpenAlexW3028601115

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.