Evidence map›Paper›PMID 34285910›Full record

ArticleBioMed research international2021

Oridonin Promotes Apoptosis and Restrains the Viability and Migration of Bladder Cancer by Impeding TRPM7 Expression via the ERK and AKT Signaling Pathways.

Xianping Che, Jiangtao Zhan, Fan Zhao, Zunhe Zhong, Mianchuan Chen, Ruifa Han, Yi Wang

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
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  5. Oridonin fromFood science & nutrition · 2024
    Review
  6. The Role of TRPM7 in Oncogenesis.International journal of molecular sciences · 2024
    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

7 authors at 2 institutions in 1 country.

Xianping CheDepartment of Urology, The Second Affiliated Hospital of Hainan Medical University, 570311 Hainan, China.ORCID https://orcid.org/0000-0002-8601-6614
Jiangtao ZhanDepartment of Urology, The Second Affiliated Hospital of Hainan Medical University, 570311 Hainan, China.ORCID https://orcid.org/0000-0003-4850-9626
Fan ZhaoDepartment of Urology, The Second Affiliated Hospital of Hainan Medical University, 570311 Hainan, China.
Zunhe ZhongDepartment of Urology, The Second Affiliated Hospital of Hainan Medical University, 570311 Hainan, China.ORCID https://orcid.org/0000-0001-5969-4121
Mianchuan ChenDepartment of Urology, The Second Affiliated Hospital of Hainan Medical University, 570311 Hainan, China.
Ruifa HanDepartment of Urology, The Second Hospital of Tianjin Medical University, Tianjin Institute of Urology, 300211 Tianjin, China.ORCID https://orcid.org/0000-0001-9677-8789
Yi WangDepartment of Urology, The Second Affiliated Hospital of Hainan Medical University, 570311 Hainan, China.ORCID https://orcid.org/0000-0001-7152-0757
Hainan Medical University · CNSecond Hospital of Tianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOridonin is a powerful anticancer compound found in

methodsThe anticancer activity of oridonin was assessed in vitro with a CCK8 assay, an annexin V-FITC apoptosis analysis, and colony formation and Transwell migration assays which were performed with the human bladder cancer cell line T24. Levels of apoptosis-related proteins, melastatin transient receptor potential channel 7 (TRPM7), and signaling molecules were examined in oridonin-treated T24 cells by western blotting or RT-PCR. Oridonin anticancer efficacy was further validated in vivo with a T24 xenograft mouse model.

resultsOridonin repressed the proliferative, colony-forming, and migratory capacities of T24 cells, triggered extensive apoptosis in vitro, and retarded tumor growth in vivo. Moreover, oridonin treatment significantly increased expression levels of p53 and cleaved caspase-3 and reduced expression of TRPM7, p-AKT, and p-ERK.

conclusionOridonin exhibited outstanding antiproliferative and antimigratory effects on bladder cancer, and these effects were at least partially associated with targeting of TRPM7 through inactivation of the ERK and AKT signaling pathways. These findings provide insight for the clinical application of oridonin in bladder cancer prevention.

Indexed as

ApoptosisCell MovementMAP Kinase Signaling SystemAnimalsCell Line, TumorCell ProliferationCell SurvivalDiterpenes, KauraneFemaleHumansMiceMice, Inbred C57BLProtein Serine-Threonine KinasesProto-Oncogene Proteins c-aktTRPM Cation ChannelsTumor Stem Cell AssayDiterpenes, KauraneoridoninProtein Serine-Threonine KinasesProto-Oncogene Proteins c-aktTRPM7 protein, humanTRPM Cation Channels

Identifiers

PMID34285910
PMCPMC8275389
OpenAlexW3178669545

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.