Evidence map›Paper›PMID 26955262›Full record

ArticleDrug design, development and therapy2016

Calycosin inhibits migration and invasion through modulation of transforming growth factor beta-mediated mesenchymal properties in U87 and U251 cells.

Xiao-hu Nie, Jia Ou-yang, Ying Xing, Dan-yan Li, Ru-en Liu, Ru-xiang Xu

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.7field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

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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 2 institutions in 1 country.

Xiao-hu NieDepartment of Neurosurgery, Huzhou Central Hospital, Huzhou, Zhejiang, People's Republic of China.
Jia Ou-yangNanchang University Medical College, Nanchang, Jiangxi, People's Republic of China.
Ying XingDepartment of Gastroenterology, The 98th Hospital of Nanjing Military Command, Huzhou, Zhejiang, People's Republic of China.
Dan-yan LiSpleen & Stomach Institute, Guangzhou University of Traditional Chinese Medicine, Guangzhou, Guangdong, People's Republic of China.
Ru-en LiuDepartment of Neurosurgery, China-Japan Friendship Hospital, Beijing, People's Republic of China.
Ru-xiang XuBayi Brain Hospital, The Military General Hospital of Beijing PLA, Beijing, People's Republic of China.
China-Japan Friendship Hospital · CNHuzhou Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we investigated the potential anticancer effects of calycosin against human glioblastoma cells, including the impacts on cell proliferation, apoptosis, and cell cycle distribution. We further studied its inhibitory activity on migration and invasion in U87 and U251 cells. Furthermore, transforming growth factor beta-mediated reductions of mesenchymal-associated genes/activators, matrix metalloproteinases-2, and -9 were detected in this process. Administration of calycosin in a glioblastoma xenograft model showed that calycosin could not only reduce tumor volume but also suppress transforming growth factor beta as well as its downstream molecules. These results revealed calycosin as a potential antitumor agent in human glioblastoma.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell CycleCell MovementCell ProliferationDose-Response Relationship, DrugDrug Screening Assays, AntitumorFemaleGlioblastomaHumansInfantIsoflavonesMatrix Metalloproteinase 2Matrix Metalloproteinase 9Mesenchymal Stem Cells7,3'-dihydroxy-4'-methoxyisoflavoneAntineoplastic AgentsIsoflavonesMatrix Metalloproteinase 2Matrix Metalloproteinase 9Transforming Growth Factor betacalycosinepithelial–mesenchymal transition (EMT)glioblastomainvasionmatrix metalloproteinases (MMPs)migration

Identifiers

PMID26955262
PMCPMC4769008
OpenAlexW2284079809

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.