Evidence map›Paper›PMID 27926533›Full record

ArticleOncotarget2017

Andrographolide impedes cancer stemness and enhances radio-sensitivity in oral carcinomas via miR-218 activation.

Po-Yu Yang, Pei-Ling Hsieh, Tong Hong Wang, Cheng-Chia Yu, Ming-Yi Lu, Yi-Wen Liao, Tzu-Hsin Lee, Chih-Yu Peng

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
14.2field-weighted citation impact, top 1% 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

33 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
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  7. Effects ofJournal of dental sciences · 2024
    Article
  8. Review
  9. Cytotoxic Effect ofCurrent issues in molecular biology · 2024
    Article
  10. Review
  11. Review
  12. Article
  13. Review
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  15. MicroRNAs as Modulators of Oral Tumorigenesis-A Focused Review.International journal of molecular sciences · 2021
    Review
  16. Article
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  19. Article
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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 3 institutions in 1 country.

Po-Yu YangSchool of Dentistry, Chung Shan Medical University, Taichung, Taiwan.
Pei-Ling HsiehInstitute of Oral Sciences, Chung Shan Medical University, Taichung, Taiwan.
Tong Hong WangTissue Bank, Chang Gung Memorial Hospital, Tao-Yuan, Taiwan.
Cheng-Chia YuSchool of Dentistry, Chung Shan Medical University, Taichung, Taiwan.
Ming-Yi LuSchool of Dentistry, Chung Shan Medical University, Taichung, Taiwan.
Yi-Wen LiaoSchool of Dentistry, Chung Shan Medical University, Taichung, Taiwan.
Tzu-Hsin LeeSchool of Dentistry, Chung Shan Medical University, Taichung, Taiwan.
Chih-Yu PengSchool of Dentistry, Chung Shan Medical University, Taichung, Taiwan.
Chung Shan Medical University Hospital · TWChung Shan Medical University · TWChang Gung Memorial Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current evidence suggests that oral cancer stem cells (OCSCs) possess high tumorigenic and metastatic properties as well as chemo- and radioresistance. In this study, we demonstrated that andrographolide, the main bioactive component in the medicinal plant Andrographis, significantly reduced oncogenicity and restored radio-sensitivity of ALDH1+CD44+ OCSCs. Mechanistic studies showed that andrographolide treatment increased the expression of microRNA-218 (miR-218), leading to the downregulation of Bmi1. We showed that knockdown of miR-218 in ALDH1-CD44- non-OCSCs enhanced cancer stemness, while silencing of Bmi1 significantly counteracted it. Furthermore, we found tumor growth was reduced in mice bearing xenograft tumors after andrographolide treatment via activation of miR-218/Bmi1 axis. Together, these data demonstrated that the inhibition of tumor aggressiveness in OCSCs by andrographolide was mediated through the upregulation of miR-218, thereby reducing Bmi1 expression. These findings suggest that andrographolide may be a valuable natural compound for anti-CSCs treatment of OSCC.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicCarcinoma, Squamous CellCell Line, TumorCell ProliferationCell SurvivalDiterpenesGene Expression Regulation, NeoplasticHumansMiceMicroRNAsMouth NeoplasmsNeoplastic Stem CellsPolycomb Repressive Complex 1Radiation-Sensitizing AgentsXenograft Model Antitumor AssaysandrographolideAntineoplastic Agents, PhytogenicBMI1 protein, humanDiterpenesMicroRNAsMIRN218 microRNA, humanPolycomb Repressive Complex 1Radiation-Sensitizing Agentsandrographolidecancer stemnessmiR-218oral squamous cell carcinomas

Identifiers

PMID27926533
PMCPMC5354823
OpenAlexW2557886140

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.