Evidence map›Paper›PMID 28093676›Full record

ArticleHuman cell2017

Aryl hydrocarbon receptor signaling involved in the invasiveness of LNCaP cells.

Hisamitsu Ide, Yan Lu, Jingsong Yu, Takahiro Noguchi, Mayuko Kanayama, Satoru Muto, Raizo Yamaguchi, Suguru Kawato, Shigeo Horie

Abstract read
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In one paragraph

Article in Human cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. When AHR signaling pathways meet viral infections.Cell communication and signaling : CCS · 2023
    Review
  4. Article
  5. Review
  6. Review
  7. 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

9 authors at 3 institutions in 2 countries.

Hisamitsu IdeDepartment of Urology, Teikyo University School of Medicine, Tokyo, Japan.
Yan LuDepartment of Urology, Teikyo University School of Medicine, Tokyo, Japan.
Jingsong YuDepartment of Urology, The First Affiliated Hospital of Harbin Medical University, Heilongjiang, China.
Takahiro NoguchiDepartment of Urology, Teikyo University School of Medicine, Tokyo, Japan.
Mayuko KanayamaDepartment of Urology, Juntendo University, Graduate School of Medicine, Tokyo, Japan.
Satoru MutoDepartment of Urology, Teikyo University School of Medicine, Tokyo, Japan.
Raizo YamaguchiDepartment of Urology, Teikyo University School of Medicine, Tokyo, Japan.
Suguru KawatoDepartment of Urology, Teikyo University School of Medicine, Tokyo, Japan.
Shigeo HorieDepartment of Urology, Juntendo University, Graduate School of Medicine, Tokyo, Japan. shorie@juntendo.ac.jp.
Teikyo University · JPJuntendo University · JPHarbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is now mounting evidence that the aryl hydrocarbon receptor (AhR) plays an important role in physiologic responses such as development, cell cycle regulation, immune function and also malignant transformation in various tissues. The strong nuclear AhR expression is observed in the invasive phenotype, and an elevated nuclear AhR expression is associated with a poor prognosis of human prostate cancer. On the other hand, there are conflicting results that the AhR deficiency results in increased susceptibility to prostate tumors in mouse model. In the present study, we investigated AhR expression and its role in the growth and invasiveness of human prostate cancer cells. The AhR protein expression was detected in prostate cancer cell lines and human prostate cancer tissues. A small interfering RNA targeting AhR, constitutive active AhR expression vector, and AhR agonist and antagonist were used to moderate its expression and signaling. The induction of AhR signaling attenuated invasiveness of prostate cancer cells without affecting the cellular growth rate. These results suggest that AhR signaling in prostate cancer cells facilitates invasion of these cells, and modulation with this signaling can be a potential therapeutic target of invasive tumors.

Indexed as

Cell Line, TumorGenetic Predisposition to DiseaseHumansMaleNeoplasm InvasivenessProstatic NeoplasmsReceptors, Aryl HydrocarbonSignal TransductionReceptors, Aryl HydrocarbonAryl hydrocarbon receptorInvasionProstate cancer

Identifiers

PMID28093676
OpenAlexW2574210130

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.