Evidence map›Paper›PMID 31485605›Full record

ArticleInternational journal of oncology2019

ROCK1 promotes migration and invasion of non‑small‑cell lung cancer cells through the PTEN/PI3K/FAK pathway.

Changpeng Hu, Huyue Zhou, Yali Liu, Jingbin Huang, Wuyi Liu, Qian Zhang, Qin Tang, Fangfang Sheng, Guobing Li, Rong Zhang

Open access · hybridAbstract read
In one paragraph

Article in International journal of oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 5% 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

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 85 citations in OpenAlex.

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  12. Boronic Acid-Containing 3Pharmaceuticals (Basel, Switzerland) · 2024
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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

10 authors at 4 institutions in 1 country.

Changpeng HuDepartment of Pharmacy, The Second Affiliated Hospital, Army Medical University, Chongqing 400037, P.R. China.
Huyue ZhouDepartment of Pharmacy, The Second Affiliated Hospital, Army Medical University, Chongqing 400037, P.R. China.
Yali LiuDepartment of Pharmacy, The Second Affiliated Hospital, Army Medical University, Chongqing 400037, P.R. China.
Jingbin HuangDepartment of Pharmacy, The Second Affiliated Hospital, Army Medical University, Chongqing 400037, P.R. China.
Wuyi LiuDepartment of Pharmacy, The Second Affiliated Hospital, Army Medical University, Chongqing 400037, P.R. China.
Qian ZhangDepartment of Pharmacy, The Second Affiliated Hospital, Army Medical University, Chongqing 400037, P.R. China.
Qin TangDepartment of Pharmacy, The Second Affiliated Hospital, Army Medical University, Chongqing 400037, P.R. China.
Fangfang ShengDepartment of Pharmacy, The Second Affiliated Hospital, Army Medical University, Chongqing 400037, P.R. China.
Guobing LiDepartment of Pharmacy, The Second Affiliated Hospital, Army Medical University, Chongqing 400037, P.R. China.
Rong ZhangDepartment of Pharmacy, The Second Affiliated Hospital, Army Medical University, Chongqing 400037, P.R. China.
Dalian Medical University · CNSecond Affiliated Hospital of Chongqing Medical University · CNChongqing Medical University · CNArmy Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rho‑associated protein kinase 1 (ROCK1), a member of the ROCK family, serves an important function in cell migration and invasion in neoplasms. ROCK1 has been found to be overexpressed in several types of cancers. However, the role of ROCK1 in non‑small‑cell lung cancer (NSCLC) is poorly understood. In the present study, ROCK1 was found to be overexpressed in NSCLC cells and tissues, and it was associated with poor survival of NSCLC patients. Subsequently, ROCK1 knockdown NSCLC cell lines were established using shRNA. ROCK1 knockdown significantly reduced the migration and invasion ability in the cell monolayer scratching and Transwell assays. ROCK1 knockdown was also found to markedly inhibit cell adhesion ability. Moreover, the phosphorylation of focal adhesion kinase (FAK) was inhibited by ROCK1 knockdown, reducing NSCLC cell migration and invasion ability. This mechanistic study revealed that ROCK1 significantly enhanced cell migration and invasion by inhibiting the phosphatase and tensin homolog (PTEN)/phosphoinositide 3‑kinase (PI3K)/FAK pathway. More importantly, the interruption of the PTEN/PI3K/FAK pathway markedly rescued the inhibition of cell migration and invasion mediated by ROCK1 knockdown. Taken together, these results suggest a novel role for ROCK1 in cell migration and invasion by inhibiting cell adhesion ability, and indicate that ROCK1 may be of value as a therapeutic target for the treatment of NSCLC.

Indexed as

Signal TransductionUp-RegulationA549 CellsCarcinoma, Non-Small-Cell LungCell Line, TumorCell MovementFemaleFocal Adhesion Protein-Tyrosine KinasesGene Expression Regulation, NeoplasticHumansLung NeoplasmsMaleOligonucleotide Array Sequence AnalysisPhosphatidylinositol 3-KinasesPhosphorylationPTEN PhosphohydrolaseFocal Adhesion Protein-Tyrosine KinasesPhosphatidylinositol 3-KinasesPTEN PhosphohydrolasePTEN protein, humanrho-Associated KinasesROCK1 protein, human

Identifiers

PMID31485605
PMCPMC6741846
OpenAlexW2970754665

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.