Evidence map›Paper›PMID 25873394›Full record

ArticleThe Journal of biological chemistry2015

Phosphatase and Tensin Homolog (PTEN) Represses Colon Cancer Progression through Inhibiting Paxillin Transcription via PI3K/AKT/NF-κB Pathway.

Ling-Li Zhang, Gang-Gang Mu, Qian-Shan Ding, Yan-Xia Li, Yun-bo Shi, Jin-Fen Dai, Hong-Gang Yu

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

50 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  12. [Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    Article
  13. SALL4 Oncogenic Function in Cancers: Mechanisms and Therapeutic Relevance.International journal of molecular sciences · 2022
    Review
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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

7 authors.

Ling-Li ZhangFrom the Department of Gastroenterology, Renmin Hospital of Wuhan University, 430060 Wuhan and the Departments of Gastroenterology and.
Gang-Gang MuFrom the Department of Gastroenterology, Renmin Hospital of Wuhan University, 430060 Wuhan and.
Qian-Shan DingFrom the Department of Gastroenterology, Renmin Hospital of Wuhan University, 430060 Wuhan and.
Yan-Xia LiFrom the Department of Gastroenterology, Renmin Hospital of Wuhan University, 430060 Wuhan and.
Yun-bo ShiNeurology, the First Affiliated Hospital of Zhengzhou University, 450000 Henan province, China.
Jin-Fen DaiFrom the Department of Gastroenterology, Renmin Hospital of Wuhan University, 430060 Wuhan and.
Hong-Gang YuFrom the Department of Gastroenterology, Renmin Hospital of Wuhan University, 430060 Wuhan and yhgwhu@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumor suppressor gene phosphatase and tensin homolog (PTEN) is frequently mutated in colon cancer. However, the potential contribution of loss of PTEN to colon cancer progression remains unclear. In this study, we demonstrated that PTEN overexpression or knockdown in Lovo colon cancer cells decreased or increased paxillin expression, respectively. Moreover, paxillin reversed PTEN-mediated inhibition of Lovo cell invasion and migration. Overexpression of PTEN in an orthotropic colon cancer nude mice model inhibited tumor formation and progression. In addition, PTEN protein level was negatively correlated with that of paxillin in human colon cancer tissues. Mechanistically, we identified three NF-κB binding sites on paxillin promoter and confirmed that paxillin was a direct transcriptional target of NF-κB. Our findings reveal a novel mechanism by which PTEN inhibits the progression of colon cancer by inhibiting paxillin expression downstream of PI3K/AKT/NF-κB pathway. Thereby, PTEN/PI3K/AKT/NF-κB/paxillin signaling cascade is an attractive therapeutic target for colon cancer progression.

Indexed as

AnimalsBase SequenceChromatin ImmunoprecipitationColonic NeoplasmsDisease ProgressionDNADNA PrimersHumansMiceMice, NudeNF-kappa BPaxillinPhosphatidylinositol 3-KinasesPromoter Regions, GeneticProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseDNADNA PrimersNF-kappa BPaxillinPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePten protein, mousePXN protein, humancolon cancermetastasisNF-kappa B (NF-KB)paxillinphosphatase and tensin homolog (PTEN)progressiontranscription

Identifiers

PMID25873394
PMCPMC4463446

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.