Evidence map›Paper›PMID 25955104›Full record

ArticleCancer biology & therapy2015

FOXQ1 mediates the crosstalk between TGF-β and Wnt signaling pathways in the progression of colorectal cancer.

Xudong Peng, Zan Luo, Qingjie Kang, Dawei Deng, Qiang Wang, Hongxia Peng, Shan Wang, Zhengqiang Wei

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

50 citing papers in PubMed, 82 citations in OpenAlex.

  1. Article
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  9. The transcription factor FOXQ1 in cancer.Cancer metastasis reviews · 2025
    Review
  10. Review
  11. Review
  12. Article
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  14. Review
  15. Article
  16. Article
  17. B cells in pancreatic cancer stroma.World journal of gastroenterology · 2022
    Review
  18. Article
  19. Article
  20. 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 4 institutions in 1 country.

Xudong Penga Gastrointestinal Surgical Unit; The First Affiliated Hospital of Chongqing Medical University ; Chongqing , China.
Zan Luo
Qingjie Kang
Dawei Deng
Qiang Wang
Hongxia Peng
Shan Wang
Zhengqiang Wei
Chongqing Medical University · CNFirst Affiliated Hospital of Chongqing Medical University · CNChongqing Three Gorges Central Hospital · CNSecond People’s Hospital of Yibin · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A wide variety of signaling transduction pathways contribute to tumorigenesis. Forkhead box Q1 (FOXQ1) is a member of the forkhead transcription factor family and its upregulation is closely correlated with tumor progression and prognosis of multiple cancer types, including colorectal cancer. However, the molecular mechanisms by which FOXQ1 promotes tumorigenesis, especially cancer cell invasion and metastasis in colorectal cancer, have not been fully elucidated. In the present study, we demonstrate that FOXQ1 is overexpressed in colorectal tumor tissues and its expression level is closely correlated with the stage and lymph node metastasis of colorectal cancer. In in vitro cultured SW480 colorectal cancer cells, knockdown of FOXQ1 expression by small interfering RNA greatly diminished the aggressive tumor behaviors of SW480 cells, including angiogenesis, invasion, epithelial-mesenchymal transition, and resistance to chemotherapy drug-induced apoptosis. Further mechanistic investigation showed that FOXQ1 silencing prevents the nuclear translocation of β-catenin, thus reducing the activity of Wnt signaling. Moreover, TGF-β1 induced the expression of FOXQ1 as well as the migration and invasion of SW480 cells, which was partially prevented following knockdown of FOXQ1. Our results demonstrate that FOXQ1 plays a critical role during the tumorigenesis of colorectal cancer and is a mediator of the crosstalk between Wnt and TGF-β signaling pathways. Our findings provide further insight into the cancer biology of colorectal cancer and suggest that FOXQ1 is a potential therapeutic target for the development of therapies for colorectal cancer.

Indexed as

AdultAgedAged, 80 and overBlotting, WesternCell LineCell Line, TumorCell MovementColorectal NeoplasmsDisease ProgressionEndothelial CellsFemaleForkhead Transcription FactorsGene Expression Regulation, NeoplasticHumansImmunohistochemistryMaleForkhead Transcription FactorsFOXQ1 protein, humanTransforming Growth Factor beta15-FU, 5-fluorouracil7-AAD, 7-aminoactinomycin Daggressive tumor behaviorcDNA, Complementary DNAcolorectal cancerDAPI, 4′,6-diamidino-2-phenylindoleddH2O, double distilled H2ODEPC, Diethy pyrocarbonateDMSO, Dimethyl sulfoxideEMT, Epithelial-Mesenchymal transitionepithelial-mesenchymal transitionFOXQ1FOXQ1, Forkhead Box Q1L-OHP, OxaliplatinMiRNA, MicroRNAMMP2, Matrix metalloproteinase-2NC-shRNA, Negative Control-shRNAPBS, phosphate buffered salinePBS, Phosphate buffer solutionPKA, proteinkinase APVDF, Polyvinylidene fluorideqRT-PCR, Quantitative real-time PCRRNAi, RNA interferenceSDS, Sodium dodecyl sulfonateshRNA, Short hairpin RNATBS, Tris-buffered salineTEMED, Tetra methyl ethylene diamineTGF-β1TGF-β, Transformin growth βTris, Trihydroxymethyl minomethaneVEGF-A, Vascular endothelial growth factor-AWnt signalingμg, Microgrammeμl, Microliter

Identifiers

PMID25955104
PMCPMC4623466
OpenAlexW1529040986

What OpenQuestion holds

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Registered trials

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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.