Evidence map›Paper›PMID 27803760›Full record

ArticleOxidative medicine and cellular longevity2016

Carvacrol Alleviates Prostate Cancer Cell Proliferation, Migration, and Invasion through Regulation of PI3K/Akt and MAPK Signaling Pathways.

Yun Luo, Jie-Ying Wu, Min-Hua Lu, Zhi Shi, Ning Na, Jin-Ming Di

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 81 citations in OpenAlex.

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  8. The Role of TRPM7 in Oncogenesis.International journal of molecular sciences · 2024
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  19. Mapping TRPM7 Function by NS8593.International journal of molecular sciences · 2020
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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.

Yun LuoDepartment of Urology, The 3rd Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong 510630, China.
Jie-Ying WuDepartment of Urology, The 3rd Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong 510630, China.
Min-Hua LuDepartment of Urology, The 3rd Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong 510630, China.
Zhi ShiDepartment of Cell Biology & Institute of Biomedicine, National Engineering Research Center of Genetic Medicine, Guangdong Provincial Key Laboratory of Bioengineering Medicine, College of Life Science and Technology, Jinan University, Guangzhou, Guangdong 510632, China.
Ning NaDepartment of Kidney Transplantation, The 3rd Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong 510630, China.ORCID 0000-0002-8786-7445
Jin-Ming DiDepartment of Urology, The 3rd Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong 510630, China.ORCID 0000-0003-4420-3152
Sun Yat-sen University · CNJinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TRPM7 is a potential therapeutic target for treatment of prostate cancer. In this study, we investigated the effects of nonselective TRPM7 inhibitor carvacrol on cell proliferation, migration, and invasion of prostate cancer PC-3 and DU145 cells. Our results showed that carvacrol blocked TRPM7-like currents in PC-3 and DU145 cells and reduced their proliferation, migration, and invasion. Moreover, carvacrol treatment significantly decreased MMP-2, p-Akt, and p-ERK1/2 protein expression and inhibited F-actin reorganization. Furthermore, consistently, TRPM7 knockdown reduced prostate cancer cell proliferation, migration, and invasion as well. Our study suggests that carvacrol may have therapeutic potential for the treatment of prostate cancer through its inhibition of TRPM7 channels and suppression of PI3K/Akt and MAPK signaling pathways.

Indexed as

Cell Line, TumorCell MovementCell ProliferationCymenesGene Expression Regulation, NeoplasticHumansMaleMatrix Metalloproteinase 2Microscopy, FluorescenceMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3MonoterpenesPatch-Clamp TechniquesPhosphatidylinositol 3-KinasesPhosphorylationProstatic NeoplasmscarvacrolCymenesMatrix Metalloproteinase 2Mitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3MonoterpenesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRNA, Small InterferingTrpm7 protein, ratTRPM Cation Channels

Identifiers

PMID27803760
PMCPMC5075627
OpenAlexW2529996781

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.