Evidence map›Paper›PMID 28376864›Full record

ArticleBMC complementary and alternative medicine2017

Antiangiogenic effects of oridonin.

Lili Tian, Kangjie Xie, Donglai Sheng, Xiaoqing Wan, Guofu Zhu

Open access · goldAbstract read
In one paragraph

Article in BMC complementary and alternative medicine, 2017. 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
2.1field-weighted citation impact, top 12% 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, 47 citations in OpenAlex.

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  20. Zirconium-Porphyrin PCN-222: pH-responsive Controlled Anticancer Drug Oridonin.Evidence-based complementary and alternative medicine : eCAM · 2018
    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

5 authors at 4 institutions in 1 country.

Lili TianTraditional Chinese medicine pharmacy, Zhejiang Hospital, No. 12 Lingyin Road, Xihu District, Zhejiang, Hangzhou, China.
Kangjie XieAnesthesia Department, Zhejiang Cancer Hospital, No. 38 Guangji Road, Gongshu District, Zhejiang, Hangzhou, 310002, China.
Donglai ShengInstitute of Developmental and Regenerative Biology, Hangzhou Normal University, No. 16 Xuelin Street, Jianggan District, Zhejiang, Hangzhou, 310036, China.
Xiaoqing WanTraditional Chinese medicine pharmacy, Zhejiang Hospital, No. 12 Lingyin Road, Xihu District, Zhejiang, Hangzhou, China.
Guofu ZhuSchool of Pharmacy, Shanghai University of Traditional Chinese Medicine, No. 1200 Cailun Road, Pudong New District, Shanghai, 201203, China. zgfzyy2015@sina.com.
Shanghai University of Traditional Chinese Medicine · CNHangzhou Normal University · CNZhejiang Cancer Hospital · CNZhejiang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOridonin, the major terpene found in Rabdosia rubescens (Henmsl.) Hara, is widely used as a dietary supplement and therapeutic drug. Oridonin has been proven to possess good anti-tumour activity, but little is known about its effect on angiogenesis. The aim of this study was to investigate the antiangiogenic effects of oridonin in vivo and in vitro and prove that oridonin anti-tumour activity is based on suppressing angiogenesis.

methodsIn vitro, the antiangiogenesis effect was studied by proliferation, apoptosis, migration, invasion, and tube formation experiments on human umbilical vascular endothelial cells (HUVECs). In vivo, using the Tg (fli1: GFP) zebrafish model, the embryonic vasculogenesis and postnatal regeneration were evaluated. The vascular endothelial growth factor (VEGF) signalling pathway gene expressions were assessed by reverse transcription-polymerase chain reaction (RT-PCR). Furthermore, the inhibition effects on tumour growth and metastasis were observed using a xenograft zebrafish tumour model and xenograft nude mouse tumour model. Angiogenesis was assayed by immunostaining with cluster of differentiation 31. Importantly, the proteins were identified as being differentially expressed in an in vivo model by two-dimensional electrophoresis-mass spectrometry (2D-MS) and western blot (WB).

resultsThe results indicated that oridonin inhibited HUVEC proliferation, migration, invasion, and tube formation and induced cell apoptosis. Oridonin inhibited zebrafish angiogenesis during embryonic development and tail fin regeneration. RT-PCR showed that oridonin decreased the VEGFA, VEGFR2, and VEGFR3 expressions in zebrafish, while the TP53 expression increased. Moreover, oridonin had strong effects on tumour growth and metastasis in vivo. 2D-MS identified a total of 50 proteins differentially expressed (17 up-expressed, 28 down-expressed). Lastly, WB showed that Claudin 1, Claudin 4, and Claudin 7 were closely related to tumour growth and metastasis.

conclusionThis study demonstrated that oridonin could inhibit tumour growth and metastasis, which mainly based on oridonin antiangiogenic effects. Claudin 1, Claudin 4, and Claudin 7 were the main contributors to the mechanism.

Indexed as

Angiogenesis InhibitorsAnimalsAntineoplastic Agents, PhytogenicDiterpenes, KauraneDrug Screening Assays, AntitumorFemaleHumansHuman Umbilical Vein Endothelial CellsIsodonMaleMiceMice, NudeZebrafishAngiogenesis InhibitorsAntineoplastic Agents, PhytogenicDiterpenes, KauraneoridoninAngiogenesisHUVECsMouseOridoninZebrafish

Identifiers

PMID28376864
PMCPMC5379751
OpenAlexW2605305206

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.