Evidence map›Paper›PMID 27999191›Full record

ArticleOncotarget2017

NHERF1 regulates the progression of colorectal cancer through the interplay with VEGFR2 pathway.

Yanan Gu, Hefen Yu, Chengcheng Hao, Tracey A Martin, Rachel Hargest, Junqi He, Shan Cheng, Wen G Jiang

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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. NHERF1 and tumor microenvironment: a new scene in invasive breast carcinoma.Journal of experimental & clinical cancer research : CR · 2018
    Article
  5. 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

8 authors at 2 institutions in 2 countries.

Yanan GuDepartment of Biochemistry and Molecular Biology, Capital Medical University, Beijing 100069, China.
Hefen YuDepartment of Biochemistry and Molecular Biology, Capital Medical University, Beijing 100069, China.
Chengcheng HaoDepartment of Biochemistry and Molecular Biology, Capital Medical University, Beijing 100069, China.
Tracey A MartinBeijing Key Laboratory of Cancer & Metastasis Research, Capital Medical University, Beijing 100069, China.
Rachel HargestBeijing Key Laboratory of Cancer & Metastasis Research, Capital Medical University, Beijing 100069, China.
Junqi HeDepartment of Biochemistry and Molecular Biology, Capital Medical University, Beijing 100069, China.
Shan ChengDepartment of Biochemistry and Molecular Biology, Capital Medical University, Beijing 100069, China.
Wen G JiangDepartment of Biochemistry and Molecular Biology, Capital Medical University, Beijing 100069, China.
Capital Medical University · CNCardiff University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The oncogenic role of ectopic expression of Na+/H+ exchanger regulatory factor 1 (NHERF1) was recently suggested in colorectal cancer, where it was implicated in playing a role in the tumor hypoxia microenvironment. Here we showed that a high level expression of NHERF1 was found in colorectal cancer tissues and that the expression of NHERF1 was positively correlated with VEGFR2 expression. The prognostic value of VEGFR2 expression in colorectal cancer relied on the expression of NHERF1. The up-regulation of NHERF1 induced by the exposure to hypoxia in colon cancer cells depended on the activation of VEGFR2 signaling. NHERF1 in turn inhibited the activation of VEGFR2 signaling which could be regulated by the interaction between NHERF1 and VEGFR2, resulting in the reduction of migration and invasion of colon cancer cells. These results suggest a dynamic interplay between NHERF1 and VEGFR2 signaling in colorectal cancer, which could explain the contribution of NHERF1 to the regulation of tumor cell responses to the hypoxia microenvironment.

Indexed as

Cell MovementSignal TransductionCell Line, TumorColorectal NeoplasmsDisease ProgressionFeedback, PhysiologicalHumansNeoplasm InvasivenessPhospholipase C gammaPhosphoproteinsProto-Oncogene Proteins c-aktSodium-Hydrogen ExchangersTime FactorsTumor HypoxiaTumor MicroenvironmentVascular Endothelial Growth Factor Receptor-2KDR protein, humanPhospholipase C gammaPhosphoproteinsProto-Oncogene Proteins c-aktsodium-hydrogen exchanger regulatory factorSodium-Hydrogen ExchangersVascular Endothelial Growth Factor Receptor-2colorectal cancerhypoxiaNHERF1PDZ proteinVEGFR

Identifiers

PMID27999191
PMCPMC5352358
OpenAlexW2563341817

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.