Evidence map›Paper›PMID 26397053›Full record

ArticleOncology reports2015

Trichosanthin suppresses the proliferation of glioma cells by inhibiting LGR5 expression and the Wnt/β-catenin signaling pathway.

Junjie Miao, Yilin Jiang, Dongliang Wang, Jingru Zhou, Cungang Fan, Feng Jiao, Bo Liu, Jun Zhang, Yangshuo Wang, Qingjun Zhang

Open access · hybridAbstract read
In one paragraph

Article in Oncology reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 36 citations in OpenAlex.

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  12. Therapeutic potential of natural products in glioblastoma treatment: targeting key glioblastoma signaling pathways and epigenetic alterations.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
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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

10 authors at 2 institutions in 1 country.

Junjie MiaoDepartment of Neurosurgery, Peking University People's Hospital, Beijing 100044, P.R. China.
Yilin JiangDepartment of Neurosurgery, Peking University People's Hospital, Beijing 100044, P.R. China.
Dongliang WangDepartment of Neurosurgery, Peking University People's Hospital, Beijing 100044, P.R. China.
Jingru ZhouDepartment of Neurosurgery, Peking University People's Hospital, Beijing 100044, P.R. China.
Cungang FanDepartment of Neurosurgery, Peking University People's Hospital, Beijing 100044, P.R. China.
Feng JiaoDepartment of Neurosurgery, Peking University People's Hospital, Beijing 100044, P.R. China.
Bo LiuDepartment of Neurosurgery, Peking University People's Hospital, Beijing 100044, P.R. China.
Jun ZhangDepartment of Neurosurgery, Peking University People's Hospital, Beijing 100044, P.R. China.
Yangshuo WangDepartment of Neurosurgery, Peking University People's Hospital, Beijing 100044, P.R. China.
Qingjun ZhangDepartment of Neurosurgery, Peking University People's Hospital, Beijing 100044, P.R. China.
Peking University · CNPeking University People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies have indicated that trichosanthin (TCS), a bioactive protein extracted and purified from the tuberous root of Trichosanthes kirilowii (a well‑known traditional Chinese medicinal plant), produces antitumor effects on various types of cancer cells. However, the effects of TCS on glioma cells are poorly understood. The objective of this study was to investigate the antitumor effects of TCS on the U87 and U251 cell lines. The in vitro effects of TCS on these two cell lines were determined using a Cell Counting Kit‑8 (CCK‑8) assay, Annexin V‑FITC staining, DAPI staining, Transwell assays, terminal deoxynucleotidyl transferase‑mediated dUTP nick end‑labeling (TUNEL) assays, 5,5',6,6'‑tetrachloro‑1,1',3,3'‑tetraethyl‑imidacarbocyanine iodide (JC‑1) staining and western blotting, which was utilized to assess the expression of leucine‑rich repeat‑containing G protein‑coupled receptor 5 (LGR5) and key proteins in the Wnt/β‑catenin signaling pathway. Our data indicated that TCS inhibited the proliferation of glioma cells in a dose‑ and time‑dependent manner and played a role in inhibiting glioma cell invasion and migration. Additional investigation revealed that the expression levels of LGR5 and of key proteins in the Wnt/β‑catenin signaling pathway were markedly decreased after TCS treatment. The results suggest that TCS may induce apoptosis in glioma cells by targeting LGR5 and repressing the Wnt/β‑catenin signaling pathway. In the future, in vivo experiments should be conducted to examine the potential use of this compound as a novel therapeutic agent for gliomas.

Indexed as

ApoptosisCell Line, TumorCell ProliferationCell SurvivalDrugs, Chinese HerbalGene Expression Regulation, NeoplasticGliomaHumansReceptors, G-Protein-CoupledTrichosanthesTrichosanthinWnt Signaling PathwayDrugs, Chinese HerbalLGR5 protein, humanReceptors, G-Protein-CoupledTrichosanthin

Identifiers

PMID26397053
PMCPMC4722885
OpenAlexW1895468589

What OpenQuestion holds

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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.