Evidence map›Paper›PMID 25354591›Full record

ArticleMolecular medicine reports2015

Triptolide inhibits cell proliferation and tumorigenicity of human neuroblastoma cells.

Xiaomin Yan, Xiao-Xue Ke, Hailong Zhao, Mengying Huang, Renjian Hu, Hongjuan Cui

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Frontiers in pharmacology · 2019
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Antibiotic drug tigecycline reduces neuroblastoma cells proliferation by inhibiting Akt activation in vitro and in vivo.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  11. 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

6 authors at 2 institutions in 1 country.

Xiaomin YanState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400716, P.R. China.
Xiao-Xue KeState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400716, P.R. China.
Hailong ZhaoState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400716, P.R. China.
Mengying HuangState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400716, P.R. China.
Renjian HuState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400716, P.R. China.
Hongjuan CuiState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400716, P.R. China.
Southwest University · CNState Key Laboratory of Silkworm Genomic Biology

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triptolide is a diterpene triepoxide, extracted from the Chinese herb Tripterygium wilfordii Hook F, which has been shown to have antitumor activity in a number of cancers. Neuroblastoma is an aggressive extracranial pediatric solid tumor, with significant chemotherapeutic resistance. In this study, triptolide was hypothesized to be a potential therapeutic agent for neuroblastoma. The effects of triptolide on neuroblastoma cell growth and tumor development were investigated. Cell growth and proliferation were evaluated using a cell counting kit‑8 assay and a 5-bromo-2-deoxyuridine staining assay. Cell cycle and apoptosis were detected by flow cytometry. Reverse transcription‑quantitative polymerase chain reaction was conducted to detect the expression levels of the apoptosis‑associated proteins, caspase‑3 and caspase‑9. The tumorigenicity of neuroblastoma cells was assessed by a soft agar clonogenic assay and an in vivo tumorigenic assay. The results demonstrated that exposure of BE(2)‑C human neuroblastoma cells to triptolide resulted in a reduction in cell growth and proliferation, and the induction of cell death and apoptosis, together with cell cycle arrest in the S phase. A soft agar assay indicated that triptolide inhibited the colony‑forming ability of BE(2)‑C neuroblastoma cells. The xenograft experiment showed that triptolide significantly reduced tumor growth and development in vivo. The data suggested that this Chinese herb may be a potential novel chemotherapeutic agent for neuroblastoma.

Indexed as

AnimalsAntineoplastic Agents, AlkylatingApoptosisCarcinogenesisCaspase 3Caspase 9Cell Line, TumorCell ProliferationCell SurvivalDiterpenesEpoxy CompoundsFemaleHumansMiceMice, Inbred NODMice, SCIDAntineoplastic Agents, AlkylatingCaspase 3Caspase 9DiterpenesEpoxy CompoundsPhenanthrenestriptolide

Identifiers

PMID25354591
PMCPMC4262511
OpenAlexW2001665242

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.