Evidence map›Paper›PMID 28468127›Full record

ArticleOncotarget2017

Rab11a promotes proliferation and invasion through regulation of YAP in non-small cell lung cancer.

Qianze Dong, Lin Fu, Yue Zhao, Yaming Du, Qingchang Li, Xueshan Qiu, Enhua Wang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

33 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
  3. Function and regulation of Rab GTPases in cancers.Cell biology and toxicology · 2024
    Review
  4. Article
  5. Article
  6. Article
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  8. Article
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  10. Rab11FIP1-deficient mice develop spontaneous inflammation and show increased susceptibility to colon damage.American journal of physiology. Gastrointestinal and liver physiology · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Rab GTPases: Central Coordinators of Membrane Trafficking in Cancer.Frontiers in cell and developmental biology · 2021
    Review
  20. Review
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.

Qianze DongDepartment of Pathology, First Affiliated Hospital and College of Basic Medical Science, China Medical University, Shenyang, China.
Lin FuDepartment of Pathology, First Affiliated Hospital and College of Basic Medical Science, China Medical University, Shenyang, China.
Yue ZhaoDepartment of Pathology, First Affiliated Hospital and College of Basic Medical Science, China Medical University, Shenyang, China.
Yaming DuDepartment of Cardiovascular Thoracic Surgery, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China.
Qingchang LiDepartment of Pathology, First Affiliated Hospital and College of Basic Medical Science, China Medical University, Shenyang, China.
Xueshan QiuDepartment of Pathology, First Affiliated Hospital and College of Basic Medical Science, China Medical University, Shenyang, China.
Enhua WangDepartment of Pathology, First Affiliated Hospital and College of Basic Medical Science, China Medical University, Shenyang, China.
China Medical University · CNJinzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rab11a, an evolutionarily conserved Rab GTPases, plays important roles in intracellular transport and has been implicated in cancer progression. However, its role in human non-small cell lung cancer (NSCLC) has not been explored yet. In this study, we discovered that Rab11a protein was upregulated in 57/122 NSCLC tissues. Rab11a overexpression associated with advanced TNM stage, positive nodal status and poor patient prognosis. Rab11a overexpression promoted proliferation, colony formation, invasion and migration with upregulation of cyclin D1, cyclin E, and downregulation of p27 in NSCLC cell lines. Nude mice xenograft demonstrated that Rab11a promoted in vivo cancer growth. Importantly, we found that Rab11a induced YAP protein and inhibited Hippo signaling. Depletion of YAP abolished the effects of Rab11a on cell cycle proteins and cell proliferation. Furthermore, immunoprecipitation showed that Rab11a interacted with YAP in lung cancer cells. In conclusion, the present study suggestes that Rab11a serves as an important oncoprotein and a regulator of YAP in NSCLC.

Indexed as

Cell ProliferationAdaptor Proteins, Signal TransducingAnimalsCarcinoma, Non-Small-Cell LungCell Line, TumorCell MovementCyclin D1Cyclin-Dependent Kinase Inhibitor p27Cyclin EDown-RegulationFemaleHippo Signaling PathwayHumansImmunohistochemistryLungLung NeoplasmsAdaptor Proteins, Signal TransducingCCND1 protein, humanCCNE1 protein, humanCDKN1B protein, humanCyclin D1Cyclin-Dependent Kinase Inhibitor p27Cyclin EOncogene ProteinsPhosphoproteinsProtein Serine-Threonine Kinasesrab11 GTP-Binding Proteinsrab GTP-Binding ProteinsTranscription FactorsYAP1 protein, humanYAP-Signaling ProteinsHipponon-small cell lung cancerproliferationRab11aYAP

Identifiers

PMID28468127
PMCPMC5438609
OpenAlexW2591177302

What OpenQuestion holds

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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.