Evidence map›Paper›PMID 28243729›Full record

ArticleVirchows Archiv : an international journal of pathology2017

Expression of Rab5a correlates with tumor progression in pancreatic carcinoma.

Yuandong Li, Xiaofang Sun, Donghui Ji, Xiangshun Kong, Dengxiang Liu, Zhenya Zhao, Jingbo Yan, Shubo Chen

Abstract read
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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
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  10. Article
  11. Rab5a suppresses autophagy to promote drug resistance in cancer cells.American journal of translational research · 2018
    Article
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

8 authors at 2 institutions in 1 country.

Yuandong LiDepartment of oncological Surgery, Xingtai Renmin Hospital, Xingtai, China.
Xiaofang SunDepartment of oncological Surgery, Xingtai Renmin Hospital, Xingtai, China.
Donghui JiDepartment of oncological Surgery, Xingtai Renmin Hospital, Xingtai, China.
Xiangshun KongDepartment of oncological Surgery, Xingtai Renmin Hospital, Xingtai, China.
Dengxiang LiuDepartment of oncological Surgery, Xingtai Renmin Hospital, Xingtai, China.
Zhenya ZhaoDepartment of pathology, Xingtai Renmin Hospital, Xingtai, China.
Jingbo YanDepartment of pathology, Xingtai Renmin Hospital, Xingtai, China.
Shubo ChenDepartment of oncological Surgery, Xingtai Renmin Hospital, Xingtai, China. liyuandongxt@sina.com.
Hebei Medical University · CNXingtai People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rab family protein Rab5a has been implicated in cancer progression. To date, its expression pattern in human pancreatic cancer has not been investigated. This study aims to examine clinical significance, biological role, and potential mechanism of action of mRab5a in human pancreatic cancer. We analyzed Rab5a protein in cancer tissue of 111 cases of pancreatic cancer using immunohistochemistry. The results show that Rab5a overexpression correlates with high T stage, positive nodal status, and advanced TNM stage. We performed knockdown of Rab5a through transfection of Rab5a-specific siRNA in the Capan-2 cell line, which shows high endogenous expression, and of Rab5a plasmid in the CFPAC-1 cell line, which shows low endogenous expression. Rab5a knockdown inhibited cell proliferation and invasion while its overexpression promoted cell proliferation and invasion. In addition, overexpression of Rab5a induced resistance to 5-FU and gemcitabine while its knockdown reduced resistance to 5-FU and gemcitabine. Furthermore, our results show that Rab5a overexpression upregulates Wnt signaling and expression of Wnt target genes including c-myc and MMP7. Blocking Wnt signaling abolished the effects of Rab5a on Wnt targets and on cancer cell proliferation. In summary, our results show that Rab5a is overexpressed in pancreatic cancer and promotes aggressive biological behavior through regulation of the Wnt/β-catenin signaling pathway.

Indexed as

Biomarkers, TumorBlotting, WesternCarcinoma, Pancreatic DuctalDisease ProgressionGene Knockdown TechniquesHumansImmunohistochemistryPancreatic NeoplasmsPrognosisrab5 GTP-Binding ProteinsReal-Time Polymerase Chain ReactionWnt Signaling PathwayBiomarkers, TumorRAB5C protein, humanrab5 GTP-Binding ProteinsChemoresistancePancreatic cancerRab5aWnt

Identifiers

PMID28243729
OpenAlexW2592003067

What OpenQuestion holds

Textmetadata
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.