Evidence map›Paper›PMID 27659528›Full record

ArticleOncotarget2016

Geridonin and paclitaxel act synergistically to inhibit the proliferation of gastric cancer cells through ROS-mediated regulation of the PTEN/PI3K/Akt pathway.

Sai-Qi Wang, Cong Wang, Li-Ming Chang, Kai-Rui Zhou, Jun-Wei Wang, Yu Ke, Dong-Xiao Yang, Hong-Ge Shi, Ran Wang, Xiao-Li Shi and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

36 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
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  4. Article
  5. LncRNAs in modulating cancer cell resistance to paclitaxel (PTX) therapy.Medical oncology (Northwood, London, England) · 2024
    Review
  6. Review
  7. Article
  8. Mechanisms of cancer cell death induction by paclitaxel: an updated review.Apoptosis : an international journal on programmed cell death · 2022
    Review
  9. Article
  10. Review
  11. Preclinical studies of the triazolo[1,5-Acta pharmaceutica Sinica. B · 2022
    Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
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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

12 authors at 1 institution in 1 country.

Sai-Qi WangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Cong WangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Li-Ming ChangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Kai-Rui ZhouSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Jun-Wei WangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Yu KeSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Dong-Xiao YangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Hong-Ge ShiSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Ran WangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Xiao-Li ShiSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Li-Ying MaSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Hong-Min LiuSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paclitaxel, a taxane, is a cytotoxic chemotherapeutic agent that targets microtubules. It has become a front-line therapy for a broad range of malignancies, including lung, breast, gastric, esophageal, and bladder carcinomas. Although paclitaxel can inhibit tumor development and improve survival, poor solubility, myelotoxicity, allergic reactions, and drug resistance have restricted its clinical application. Paclitaxel is frequently combined with other chemotherapeutics to enhance the antitumor effects and reduce side effects. We synthesized geridonin, a derivative of oridonin, and demonstrate that geridonin and paclitaxel act synergistically to inhibit the growth of gastric cancer cells. Importantly, geridonin enhanced the antitumor effects of paclitaxel without increasing toxicity in vivo. Mechanistic analysis revealed that administration of geridonin in combination with paclitaxel up-regulated the tumor suppressor PTEN and inhibited phosphorylation of Akt and MDM2. This led to the accumulation of p53 and induced apoptosis though the mitochondrial pathway. Thus, geridonin in combination with paclitaxel is a new treatment strategy for gastric cancer.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell Line, TumorCell ProliferationDisease Models, AnimalDiterpenes, KauraneDrug SynergismHumansMaleMembrane Potential, MitochondrialMicePaclitaxelPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseAntineoplastic AgentsDiterpenes, KauranegeridoninPaclitaxelPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanReactive Oxygen Speciesgastric canceroridoninpaclitaxel resistancePI3K/Akt pathwaysynergism

Identifiers

PMID27659528
PMCPMC5341958
OpenAlexW2522277966

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.