Evidence map›Paper›PMID 27748883›Full record

ArticleOncology reports2016

Effect of RhoC on the epithelial-mesenchymal transition process induced by TGF-β1 in lung adenocarcinoma cells.

Xiaoxiao Lu, Honglan Guo, Xi Chen, Jian Xiao, Yong Zou, Wei Wang, Qiong Chen

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in Oncology reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. TGF-β signaling in health, disease, and therapeutics.Signal transduction and targeted therapy · 2024
    Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. CCNA2 facilitates epithelial-to-mesenchymal transition via the integrin αvβ3 signaling in NSCLC.International journal of clinical and experimental pathology · 2017
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Xiaoxiao LuDepartment of Geriatrics, Xiangya Hospital of Central South University, Changsha, Hunan 410008, P.R. China.
Honglan GuoDepartment of Geriatrics, Xiangya Hospital of Central South University, Changsha, Hunan 410008, P.R. China.
Xi ChenDepartment of Respiratory Medicine, Xiangya Hospital of Central South University, Changsha, Hunan 410008, P.R. China.
Jian XiaoDepartment of Geriatrics, Xiangya Hospital of Central South University, Changsha, Hunan 410008, P.R. China.
Yong ZouDepartment of Geriatrics, Xiangya Hospital of Central South University, Changsha, Hunan 410008, P.R. China.
Wei WangDepartment of Nephrology Medicine, Huaihe Hospital of Henan University, Kaifeng, Henan 475000, P.R. China.
Qiong ChenDepartment of Geriatrics, Xiangya Hospital of Central South University, Changsha, Hunan 410008, P.R. China.
Central South University · CNXiangya Hospital Central South University · CNHenan University Huaihe Hospital and Huaihe Clinical Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

According to recent research, Ras homolog gene family member C (RhoC) is confirmed to have a powerful regulatory effect on cell motility mediated by the cytoskeleton, and this process is closely associated with tumor invasion and metastasis. In addition, the epithelial-mesenchymal transition (EMT) process which causes cytoskeleton rearrangement, also plays a pivotal role in tumor invasion and metastasis.Consequently, in the present study, we aimed to ascertain whether RhoC has an effect on the EMT process induced by TGF-β1 in lung adenocarcinoma cells and whether RhoC promotes tumor invasion by mediating the occurrence of EMT. Based on the findings, we demonstrated that RhoC was an essential mediator of the EMT process in lung adenocarcinoma cell line A549 which was evaluated by observing the morphological characteristics of the cells and by assessing the expression levels of two EMT marker proteins: E-cadherin and vimentin. During the process of EMT in the A549 cells induced by TGF-β1 (5 ng/ml), upregulated RhoC protein and RhoC activity were detected, which was associated with the enhanced invasive capability of the cells in vitro. Conversely, downregulation of the expression of RhoC by shRNA markedly impeded EMT progression as well as the invasion of A549 cells. Our results may provide a novel target towards the prevention of metastasis in advanced lung adenocarcinoma.

Indexed as

Epithelial-Mesenchymal TransitionA549 CellsAdenocarcinomaAdenocarcinoma of LungCell MovementCytoskeletonGene ExpressionHumansLung NeoplasmsNeoplasm InvasivenessrhoC GTP-Binding Proteinrho GTP-Binding ProteinsTransforming Growth Factor beta1rhoC GTP-Binding ProteinRHOC protein, humanrho GTP-Binding ProteinsTransforming Growth Factor beta1

Identifiers

PMID27748883
PMCPMC5112615
OpenAlexW2529225720

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.