Evidence map›Paper›PMID 30975734›Full record

ArticleBioscience reports2019

L-securinine inhibits cell growth and metastasis of human androgen-independent prostate cancer DU145 cells via regulating mitochondrial and AGTR1/MEK/ERK/STAT3/PAX2 apoptotic pathways.

Dongxu Zhang, Houxian Liu, Binbin Yang, Jiasheng Hu, Yue Cheng

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 28 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

5 authors at 1 institution in 1 country.

Dongxu ZhangDepartment of Urological Surgery, Ningbo First Hospital, Ningbo Hospital of Zhejiang University, Ningbo 315010, China.
Houxian LiuDepartment of Urological Surgery, Ningbo Fenghua District People's Hospital, Ningbo 315500, China.
Binbin YangDepartment of Urological Surgery, Ningbo First Hospital, Ningbo Hospital of Zhejiang University, Ningbo 315010, China binbinyangvip@gmail.com.ORCID 0000-0002-3290-0121
Jiasheng HuDepartment of Urological Surgery, Ningbo First Hospital, Ningbo Hospital of Zhejiang University, Ningbo 315010, China.
Yue ChengDepartment of Urological Surgery, Ningbo First Hospital, Ningbo Hospital of Zhejiang University, Ningbo 315010, China.
Ningbo First Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study aims to evaluate the anticancer effect of L-securinine on androgen-independent prostate cancer (AIPC) DU145 cells. L-securinine (2.5, 5, and 10 μM) treatment for 24, 48 and 72 h displayed strong growth inhibitory effect on DU145 cells in a concentration and time-dependent fashion but has less toxicity toward normal androgen-dependent LNCaP cells. Hoechst 332582 staining of DU145 cells and Annexin V-FITC/ PI dual-labeling followed by flow cytometry assay identified that this growth inhibition by L-securinine would be due to the induction of apoptosis. Moreover Transwell assay revealed that L-securinine significantly inhibited the cell migration/invasion ability of DU145 cells. Furthermore, results of western blotting showed that the involvement of mitochondrial apoptotic pathway in the L-securinine-induced apoptosis of DU145 cell, as evidenced by an increase in the protein expression of Bax, cleaved caspase-9, cleaved caspase-3, cytosolic cytochrome c, and cleaved PARP, together with a unchanged cleaved caspase-8 and decreased Bcl-2 protein expression. Also, L-securinine-induced antimetastatic activity in DU145 cells was associated with decreased protein expression of MMP-2 and MMP-9 and concurrent reduction of VEGF. In addition, further studies revealed that L-securinine may inhibit the protein expression of AGTR1, p-MEK1/2, p-ERK1/2, p-STAT3, PAX2, and p-PAX2, while the expression of ERK1/2, MEK1/2, and STAT3 protein retains intact. These findings suggest that L-securinine may be a promising chemopreventive agent against AIPC.

Indexed as

Antineoplastic Agents, PhytogenicApoptosisAzepinesbcl-2-Associated X ProteinCaspase 3Caspase 9Cell CycleCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticHeterocyclic Compounds, Bridged-RingHumansLactonesMaleMAP Kinase Kinase 1AGTR1 protein, humanAntineoplastic Agents, PhytogenicAzepinesBAX protein, humanbcl-2-Associated X ProteinCASP3 protein, humanCASP9 protein, humanCaspase 3Caspase 9Heterocyclic Compounds, Bridged-RingLactonesMAP2K1 protein, humanMAP2K2 protein, humanMAPK1 protein, humanMAPK3 protein, humanMAP Kinase Kinase 1MAP Kinase Kinase 2Mitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3PAX2 protein, humanPAX2 Transcription FactorPiperidinesReceptor, Angiotensin, Type 1securinineSTAT3 protein, humanSTAT3 Transcription FactorAndrogen-independent prostate cancer (AIPC)ApoptosisL-securinineMitochondrial apoptotic pathway

Identifiers

PMID30975734
PMCPMC6509055
OpenAlexW2938231860

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.