Evidence map›Paper›PMID 25823663›Full record

ArticleOncotarget2015

High expression of small GTPase Rab3D promotes cancer progression and metastasis.

Jian Yang, Wei Liu, Xin'an Lu, Yan Fu, Lin Li, Yongzhang Luo

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
4.4field-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

57 citing papers in PubMed, 89 citations in OpenAlex.

  1. Review
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  7. Membrane trafficking alterations in breast cancer progression.Frontiers in cell and developmental biology · 2024
    Review
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  11. Insights of Endocytosis Signaling in Health and Disease.International journal of molecular sciences · 2023
    Review
  12. [miR-125b-5p inhibits proliferation and migration of osteosarcoma cells by negatively regulating RAB3D expression].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2023
    Article
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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 1 institution in 1 country.

Jian YangNational Engineering Laboratory for Anti-tumor Protein Therapeutics, Tsinghua University, Beijing, China.
Wei LiuNational Engineering Laboratory for Anti-tumor Protein Therapeutics, Tsinghua University, Beijing, China.
Xin'an LuNational Engineering Laboratory for Anti-tumor Protein Therapeutics, Tsinghua University, Beijing, China.
Yan FuNational Engineering Laboratory for Anti-tumor Protein Therapeutics, Tsinghua University, Beijing, China.
Lin LiNational Engineering Laboratory for Anti-tumor Protein Therapeutics, Tsinghua University, Beijing, China.
Yongzhang LuoNational Engineering Laboratory for Anti-tumor Protein Therapeutics, Tsinghua University, Beijing, China.
Tsinghua University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rab GTPases control exocytic and endocytic membrane trafficking such as exosomes release. As a secretory small GTPase, Rab3D is a vital regulator for protein secretion. However, the role of Rab3D in cancer was never systematically studied. The aim of this study is to examine its function and mechanism in cancer, especially metastasis. We detected protein levels of Rab3D in nine cancer cell lines and twelve types of clinical cancer specimens. Subsequently, we established in vitro migration and in vivo orthotopic metastatic mouse models to study the role of Rab3D in tumor metastasis. Here, we reported that the expression levels of Rab3D were dysregulated in cancer cells and highly correlated with tumor malignancies in the clinical samples. Increased expressions of Rab3D led to tumor invasion in vitro and lung metastasis in vivo, whereas Rab3D knockdown suppressed the tumor cell motility. Mechanistic studies revealed that Rab3D activated intracellular the AKT/GSK3β signaling to induce the EMT process. In addition, it also regulated the extracellular secretion of Hsp90α to promote tumor cell migration and invasion. These results prove that Rab3D is a key molecule to regulate tumor metastasis, suggesting that blocking the Rab3D function can be a potential therapeutic approach for cancer metastasis.

Indexed as

Cell ProliferationAnimalsApoptosisBlotting, WesternBreast NeoplasmsCell MovementFemaleFluorescent Antibody TechniqueHumansImmunoenzyme TechniquesLung NeoplasmsMiceNeoplasmsNeoplasm StagingPrognosisrab3 GTP-Binding ProteinsRAB3D protein, humanrab3 GTP-Binding ProteinsRNA, Small InterferingEMTexosomesHsp90αRab3Dtumor metastasis

Identifiers

PMID25823663
PMCPMC4484444
OpenAlexW1741277085

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.