Evidence map›Paper›PMID 31026254›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2019

Rho-Associated Protein Kinase (ROCK) Promotes Proliferation and Migration of PC-3 and DU145 Prostate Cancer Cells by Targeting LIM Kinase 1 (LIMK1) and Matrix Metalloproteinase-2 (MMP-2).

Hua Gong, Lan Zhou, Lotfi Khelfat, Guangmin Qiu, Yuemin Wang, Kaili Mao, Weihua Chen

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Rho/ROCK Pathway as a Therapeutic Target in Multiple Diseases.International journal of drug discovery and pharmacology · 2025
    Article
  4. Article
  5. Role of miRNA‑122 in cancer (Review).International journal of oncology · 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 3 institutions in 2 countries.

Hua GongDepartment of Urology, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China (mainland).
Lan ZhouDepartment of Urology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, China (mainland).
Lotfi KhelfatDepartment of Urology, Cochin Hospital, Paris, France.
Guangmin QiuDepartment of Urology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, China (mainland).
Yuemin WangDepartment of Urology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, China (mainland).
Kaili MaoDepartment of Urology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, China (mainland).
Weihua ChenDepartment of Urology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, China (mainland).
Shanghai East Hospital · CNHôpital Cochin · FRShanghai University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND In the pathogenesis and progression of prostate cancer, cell proliferation and cell migration results in tumor invasion and metastasis that is associated with patient morbidity and mortality. Rho-associated protein kinase (ROCK) has previously been shown to be upregulated in prostate cancer, but its biological role remains poorly understood. This study aimed to investigate the role of ROCK in the proliferation and migration of PC-3 and DU145 prostate cancer cells and to identify the possible targets involved by knockdown of ROCK1 and ROCK2 RNA expression. MATERIAL AND METHODS An RNA interference (RNAi) assay was performed to silence the expression of ROCK1 and ROCK2 in the PC-3 and DU145 human prostate cancer cell lines. Cells were also treated with a specific ROCK inhibitor, Y27632. A cell counting kit-8 (CCK-8) assay was used to determine the proliferation rate of prostate cancer cells, and cell migration and invasion assays were performed. Western blot and polymerase chain reaction were used to measure protein and RNA expression levels. RESULTS In PC-3 and DU145 prostate cancer cells, knockdown of ROCK1 and ROCK2 reduced cell migration and invasion. ROCK1 and ROCK2 regulated cell proliferation in PC-3 and DU145 prostate cancer cells. Protein levels of phosphorylated LIM kinase 1 (p-LIMK1) and matrix metalloproteinase-2 (MMP-2) were reduced in ROCK1 and ROCK2 siRNA transfected cells. CONCLUSIONS In PC-3 and DU145 human prostate cancer cells, ROCK promoted cell proliferation and migration by targeting LIMK1 and MMP-2.

Indexed as

AdenocarcinomaAnimalsCell Line, TumorCell MovementCell ProliferationGene Knockdown TechniquesHumansLim KinasesLung NeoplasmsMaleMatrix Metalloproteinase 2MiceMice, NudePC-3 CellsProstatic Neoplasmsrho-Associated KinasesLIMK1 protein, humanLim KinasesMatrix Metalloproteinase 2MMP2 protein, humanrho-Associated KinasesRNA, Small InterferingROCK1 protein, humanROCK2 protein, human

Identifiers

PMID31026254
PMCPMC6500105
OpenAlexW2941848389

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.