Evidence map›Paper›PMID 26958938›Full record

ArticleOncotarget2016

Bufalin suppresses hepatocellular carcinoma invasion and metastasis by targeting HIF-1α via the PI3K/AKT/mTOR pathway.

Haiyong Wang, Chenyue Zhang, Litao Xu, Kun Zang, Zhouyu Ning, Feng Jiang, Huiying Chi, Xiaoyan Zhu, Zhiqiang Meng

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

59 citing papers in PubMed, 109 citations in OpenAlex.

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  19. New guaiane-type sesquiterpenoid dimers fromActa pharmaceutica Sinica. B · 2021
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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

9 authors at 5 institutions in 1 country.

Haiyong WangDepartment of Integrative Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Chenyue ZhangDepartment of Integrative Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Litao XuDepartment of Integrative Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Kun ZangDepartment of Integrative Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Zhouyu NingDepartment of Integrative Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Feng JiangDepartment of Integrative Oncology, Zhucheng Hospital of TCM, Zhucheng 262200, China.
Huiying ChiShanghai Geriatric Institute of Chinese Medicine, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200031, China.
Xiaoyan ZhuDepartment of Integrative Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Zhiqiang MengDepartment of Integrative Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Fudan University Shanghai Cancer Center · CNShanghai Medical College of Fudan University · CNLonghua Hospital Shanghai University of Traditional Chinese Medicine · CNShandong First Medical University · CNYancheng Third People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has been reported that there are multiple mechanisms by which bufalin could exert its antimetastatic effect. HIF-1α has been reported to be involved in tumor migration and invasion by regulating EMT. However, it is not known whether bufalin could exert the antimetastatic effect by modulating HIF-1α expression in hepatocellular carcinoma. In the present study, we aimed to evaluate the antimetastatic potential of bufalin in vivo and in vitro. Our results demonstrated that the liver/lung metastases were significantly reduced in bufalin-treated mice, as tested in the orthotopic transplanted and tail vein injection tumor models. Furthermore, the epithelial-to-mesenchymal transition (EMT) was inhibited in bufalin-treated tumors, as reflected the upregulation of E-cadherin, and downregulation of N-cadherin, vimentin, Snail. Similar results were observed in SMMC7721 cells treated with bufalin. Moreover, the transforming growth factor-β1 (TGF-β1)-induced EMT was also abrogated by bufalin. Mechanistically, our study demonstrated that hypoxia-inducible factor-1α (HIF-1α) played an important role in the antimetastatic effect of bufalin in hepatocellular carcinoma. Importantly, HIF-1α expression may be regulated through the inhibition of the PI3K/AKT/mTOR pathway. Taken together, our results suggest that bufalin suppresses hepatic tumor invasion and metastasis and that this process may be related to the PI3K/AKT/mTOR/ HIF-1α axis.

Indexed as

Phosphoinositide-3 Kinase InhibitorsAnimalsAntineoplastic AgentsApoptosisBiomarkers, TumorBufanolidesCarcinoma, HepatocellularCell MovementCell ProliferationEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansHypoxia-Inducible Factor 1, alpha SubunitLiver NeoplasmsMiceMice, Inbred BALB CAKT1 protein, humanAntineoplastic AgentsBiomarkers, TumorbufalinBufanolidesHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitMTOR protein, humanPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesTransforming Growth Factor beta1bufalinhepatocellular carcinomaHIF-1αmetastasisPI3K/AKT/mTOR

Identifiers

PMID26958938
PMCPMC4991447
OpenAlexW2294409638

What OpenQuestion holds

Textmetadata
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.