Evidence map›Paper›PMID 26408176›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

Fangchinoline suppresses the growth and invasion of human glioblastoma cells by inhibiting the kinase activity of Akt and Akt-mediated signaling cascades.

Bingyu Guo, Peng Xie, Jingyuan Su, Tingting Zhang, Xiaoming Li, Guobiao Liang

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  4. A critical review: traditional uses, phytochemistry, pharmacology and toxicology ofPhytochemistry reviews : proceedings of the Phytochemical Society of Europe · 2020
    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

6 authors at 1 institution in 1 country.

Bingyu GuoInstitute of Neurological Medicine, General Hospital of Shenyang Military Command, 83#Wenhua Road, Shenhe District, Shenyang, Liaoning, 110016, China.
Peng XieInstitute of Neurological Medicine, General Hospital of Shenyang Military Command, 83#Wenhua Road, Shenhe District, Shenyang, Liaoning, 110016, China.
Jingyuan SuInstitute of Neurological Medicine, General Hospital of Shenyang Military Command, 83#Wenhua Road, Shenhe District, Shenyang, Liaoning, 110016, China.
Tingting ZhangInstitute of Neurological Medicine, General Hospital of Shenyang Military Command, 83#Wenhua Road, Shenhe District, Shenyang, Liaoning, 110016, China.
Xiaoming LiInstitute of Neurological Medicine, General Hospital of Shenyang Military Command, 83#Wenhua Road, Shenhe District, Shenyang, Liaoning, 110016, China. lxm5668sw@yahoo.com.
Guobiao LiangInstitute of Neurological Medicine, General Hospital of Shenyang Military Command, 83#Wenhua Road, Shenhe District, Shenyang, Liaoning, 110016, China.
General Hospital of Shenyang Military Region · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is one of the most palindromic and malignant central nervous system neoplasms, and the current treatment is not effectual for GBM. Research of specific medicine for GBM is significant. Fangchinoline possesses a wide range of pharmacological activities and attracts more attentions due to its anti-tumor effects. In this study, two WHO grade IV human GBM cell lines (U87 MG and U118 MG) were exposed to fangchinoline, and we found that fangchinoline specifically inhibits the kinase activity of Akt and markedly suppresses the phosphorylation of Thr308 and Ser473 of Akt in human GBM cells. We also observed that fangchinoline inhibits tumor cell proliferation and invasiveness and induces apoptosis through suppressing the Akt-mediated signaling cascades, including Akt/p21, Akt/Bad, and Akt/matrix metalloproteinases (MMPs). These data demonstrated that fangchinoline exerts its anti-tumor effects in human glioblastoma cells, at least partly by inhibiting the kinase activity of Akt and suppressing Akt-mediated signaling cascades.

Indexed as

ApoptosisBenzylisoquinolinesBrain NeoplasmsCell Line, TumorCell MovementCell ProliferationGlioblastomaHumansPhosphorylationProto-Oncogene Proteins c-aktSignal TransductionBenzylisoquinolinesfangchinolineProto-Oncogene Proteins c-aktAktFangchinolineGlioblastoma multiformePhosphorylationSignaling cascade

Identifiers

PMID26408176
OpenAlexW2103392037

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.