Evidence map›Paper›PMID 30050147›Full record

ArticleScientific reports2018

Flavonoids inhibit cell proliferation and induce apoptosis and autophagy through downregulation of PI3Kγ mediated PI3K/AKT/mTOR/p70S6K/ULK signaling pathway in human breast cancer cells.

Hong-Wei Zhang, Jin-Jiao Hu, Ruo-Qiu Fu, Xin Liu, Yan-Hao Zhang, Jing Li, Lei Liu, Yu-Nong Li, Qin Deng, Qing-Song Luo and 2 more

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 151 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
151citing papers in PubMed, 1 pooled it
16.5field-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

151 citing papers in PubMed, 1 synthesis or guideline pooled it, 259 citations in OpenAlex.

  1. Pooled it
  2. Review
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  7. Review
  8. Review
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  16. Review
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  20. Article

91 more citing papers are in PubMed but not listed here.

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

12 authors at 1 institution in 1 country.

Hong-Wei ZhangCollege of Pharmacy, 3rd Military Medical University, Chongqing, 400038, China.
Jin-Jiao HuCollege of Pharmacy, 3rd Military Medical University, Chongqing, 400038, China.
Ruo-Qiu FuCollege of Pharmacy, 3rd Military Medical University, Chongqing, 400038, China.
Xin LiuCollege of Pharmacy, 3rd Military Medical University, Chongqing, 400038, China.
Yan-Hao ZhangCollege of Pharmacy, 3rd Military Medical University, Chongqing, 400038, China.
Jing LiCollege of Pharmacy, 3rd Military Medical University, Chongqing, 400038, China.
Lei LiuCollege of Pharmacy, 3rd Military Medical University, Chongqing, 400038, China.
Yu-Nong LiCollege of Pharmacy, 3rd Military Medical University, Chongqing, 400038, China.
Qin DengCollege of Pharmacy, 3rd Military Medical University, Chongqing, 400038, China.
Qing-Song LuoCollege of Pharmacy, 3rd Military Medical University, Chongqing, 400038, China.
Qin OuyangCollege of Pharmacy, 3rd Military Medical University, Chongqing, 400038, China.
Ning GaoCollege of Pharmacy, 3rd Military Medical University, Chongqing, 400038, China. gaoning59@163.com.
Army Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anticancer activities of flavonoids derived from Tephroseris kirilowii (Turcz.) Holub. were evaluated in human cancer cells. We isolated and identified, for the first time, eight flavonoids from T. kirilowii and found that three of them (IH: isorhamnetin, GN: genkwanin, and Aca: acacetin) inhibited cell proliferation in a variety of human cancer cell lines. These active flavonoids caused cell cycle arrest at G2/M phase and induced apoptosis and autophagy in human breast cancer cells. Molecular docking revealed that these flavonoids dock in the ATP binding pocket of PI3Kγ. Importantly, treatment with these flavonoids decreased the levels of PI3Kγ-p110, phospho-PI3K, phospho-AKT, phospho-mTOR, phospho-p70S6K, and phospho-ULK. Pretreatment with PI3Kγ specific inhibitor AS605240 potentiated flavonoids-mediated inactivation of AKT, mTOR, p70S6K, ULK, and apoptosis. Taken together, these findings represent a novel mechanism by which downregulation of PI3Kγ-p110 and consequent interruption of PI3K/AKT/mTOR/p70S6K/ULK signaling pathway might play a critical functional role in these flavonoids-induced cell cycle arrest at G2/M phase, apoptosis, and autophagy. Our studies provide novel insights into the anticancer activities of selected flavonoids and their potential uses in anticancer therapy.

Indexed as

Phosphoinositide-3 Kinase InhibitorsAntineoplastic AgentsApoptosisAutophagyAutophagy-Related Protein-1 HomologCell Line, TumorCell ProliferationClass Ib Phosphatidylinositol 3-KinaseDown-RegulationFlavonoidsHumansIntracellular Signaling Peptides and ProteinsOncogene Protein v-aktRibosomal Protein S6 Kinases, 70-kDaSignal TransductionTOR Serine-Threonine KinasesAntineoplastic AgentsAutophagy-Related Protein-1 HomologClass Ib Phosphatidylinositol 3-KinaseFlavonoidsIntracellular Signaling Peptides and ProteinsMTOR protein, humanOncogene Protein v-aktPhosphoinositide-3 Kinase InhibitorsPIK3CG protein, humanRibosomal Protein S6 Kinases, 70-kDaTOR Serine-Threonine KinasesULK1 protein, human

Identifiers

PMID30050147
PMCPMC6062549
OpenAlexW2883624246

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.