Evidence map›Paper›PMID 30150684›Full record

ArticleScientific reports2018

Antrodia cinnamomea boosts the anti-tumor activity of sorafenib in xenograft models of human hepatocellular carcinoma.

Wei-De Wu, Pin-Shern Chen, Hany A Omar, El-Shaimaa A Arafa, Hung-Wei Pan, Jingyueh Jeng, Jui-Hsiang Hung

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Acta pharmaceutica Sinica. B · 2022
    Article
  5. Article
  6. Article
  7. Effect of ethanol extracts of Antrodia cinnamomea on head and neck squamous cell carcinoma cell line.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2020
    Article
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 3 countries.

Wei-De WuDepartment of Biotechnology, Chia Nan University of Pharmacy and Science, Tainan, Taiwan.
Pin-Shern ChenDepartment of Biotechnology, Chia Nan University of Pharmacy and Science, Tainan, Taiwan.
Hany A OmarSharjah Institute for Medical Research and College of Pharmacy, University of Sharjah, Sharjah, UAE.ORCID 0000-0002-4670-8149
El-Shaimaa A ArafaDepartment of Clinical Sciences, College of Pharmacy, Ajman University, Ajman, UAE.ORCID 0000-0002-9034-6624
Hung-Wei PanDepartment of Medical Education and Research, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.
Jingyueh JengDepartment of Biotechnology, Chia Nan University of Pharmacy and Science, Tainan, Taiwan.
Jui-Hsiang HungDepartment of Biotechnology, Chia Nan University of Pharmacy and Science, Tainan, Taiwan. hung86@mail.cnu.edu.tw.ORCID 0000-0002-7649-4823
Chia Nan University of Pharmacy and Science · TWBeni-Suef University · EGKaohsiung Veterans General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) has been recognized worldwide as one of the major causes of cancer death. The medicinal fungus Antrodia cinnamomea (A. cinnamomea) has been served as a functional food for liver protection. The aim of the present study was to investigate the potential activity of A. cinnamomea extracts as a safe booster for the anticancer activity of sorafenib, a multi-kinase inhibitor approved for the treatment of HCC. The biologically active triterpenoids in the ethanolic extracts of A. cinnamomea (EAC) were initially identified by HPLC/LC/MS then the different extracts and sorafenib were assessed in vitro and in vivo. EAC could effectively sensitize HCC cells to low doses of sorafenib, which was perceived via the ability of the combination to repress cell viability and to induce cell cycle arrest and apoptosis in HCC cells. The ability of EAC to enhance sorafenib activity was mediated through targeting mitogen-activated protein (MAP) kinases, modulating cyclin proteins expression and inhibiting cancer cell invasion. Moreover, the proposed combination significantly suppressed ectopic tumor growth in mice with high safety margins compared to single-agent treatment. Thus, this study highlights the advantage of combining EAC with sorafenib as a potential adjuvant therapeutic strategy against HCC.

Indexed as

AnimalsAnnexin A5AntrodiaApoptosisCarcinoma, HepatocellularCell CycleCell Line, TumorCell SurvivalChromatography, LiquidHep G2 CellsHumansImmunoblottingLiver NeoplasmsMiceMice, Inbred BALB CPlant ExtractsAnnexin A5Plant ExtractsPropidiumSorafenib

Identifiers

PMID30150684
PMCPMC6110745
OpenAlexW2888052802

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.