Evidence map›Paper›PMID 34697150›Full record

ArticleIn vivo (Athens, Greece)

[6]-Gingerol Suppresses Oral Cancer Cell Growth by Inducing the Activation of AMPK and Suppressing the AKT/mTOR Signaling Pathway.

Haibo Zhang, Eungyung Kim, Junkoo Yi, Huang Hai, Hyeonjin Kim, Sijun Park, Su-Geun Lim, Si-Yong Kim, Soyoung Jang, Kirim Kim and 4 more

Open access · diamondAbstract read
In one paragraph

Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 31 citations in OpenAlex.

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  10. [Cordycepin, a metabolite ofNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2023
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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

14 authors at 2 institutions in 1 country.

Haibo ZhangDepartment of Animal Science and Biotechnology, ITRD, Kyungpook National University, Sangju, Republic of Korea.
Eungyung KimDepartment of Animal Science and Biotechnology, ITRD, Kyungpook National University, Sangju, Republic of Korea.
Junkoo YiGyeongsangbukdo Livestock Institute Research, Yeongju, Republic of Korea.
Huang HaiDepartment of Animal Science and Biotechnology, ITRD, Kyungpook National University, Sangju, Republic of Korea.
Hyeonjin KimDepartment of Animal Science and Biotechnology, ITRD, Kyungpook National University, Sangju, Republic of Korea.
Sijun ParkSchool of Life Science, Kyungpook National University, Daegu, Republic of Korea.
Su-Geun LimSchool of Life Science, Kyungpook National University, Daegu, Republic of Korea.
Si-Yong KimSchool of Life Science, Kyungpook National University, Daegu, Republic of Korea.
Soyoung JangSchool of Life Science, Kyungpook National University, Daegu, Republic of Korea.
Kirim KimDepartment of Dental Hygiene, Kyungpook National University, Sangju, Republic of Korea.
Eun-Kyong KimDepartment of Dental Hygiene, Kyungpook National University, Sangju, Republic of Korea.
Youngkyun LeeDepartment of Biochemistry, School of Dentistry, Kyungpook National University, Daegu, Republic of Korea.
Zaeyoung RyooSchool of Life Science, Kyungpook National University, Daegu, Republic of Korea; ok4325@knu.ac.kr jaewoong64@hanmail.net.
Myoungok KimDepartment of Animal Science and Biotechnology, ITRD, Kyungpook National University, Sangju, Republic of Korea; ok4325@knu.ac.kr jaewoong64@hanmail.net.
Kyungpook National University · KRGyeongsangnam-do Agricultural Research and Extension Services · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aim[6]-Gingerol, a compound extracted from ginger, has been studied for its therapeutic potential in various types of cancers. However, its effects on oral cancer remain largely unknown. Here, we aimed to investigate the potential anticancer activity and underlying mechanisms of [6]-gingerol in oral cancer cells. MATERIALS AND

methodsWe analyzed the antigrowth effects of [6]-gingerol in oral cancer cell lines by cell proliferation, colony formation, migration, and invasion assays. We detected cell cycle and apoptosis with flow cytometry and further explored the mechanisms of action by immunoblotting.

results[6]-Gingerol significantly inhibited oral cancer cell growth by inducing apoptosis and cell cycle G2/M phase arrest. [6]-Gingerol also inhibited oral cancer cell migration and invasion by up-regulating E-cadherin and down-regulating N-cadherin and vimentin. Moreover, [6]-gingerol induced the activation of AMPK and suppressed the AKT/mTOR signaling pathway in YD10B and Ca9-22 cells.

conclusion[6]-Gingerol exerts anticancer activity by activating AMPK and suppressing the AKT/mTOR signaling pathway in oral cancer cells. Our findings highlight the potential of [6]-gingerol as a therapeutic drug for oral cancer treatment.

Indexed as

Mouth NeoplasmsProto-Oncogene Proteins c-aktAMP-Activated Protein KinasesApoptosisCatecholsCell Line, TumorCell ProliferationFatty AlcoholsHumansSignal TransductionTOR Serine-Threonine KinasesAMP-Activated Protein KinasesCatecholsFatty AlcoholsgingerolMTOR protein, humanProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinases[6]-GingerolAKTAMPKmTORoral cancer

Identifiers

PMID34697150
PMCPMC8627739
OpenAlexW3211132536

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.