Evidence map›Paper›PMID 26587829›Full record

ArticleOncotarget2015

Infiltrating T cells promote renal cell carcinoma (RCC) progression via altering the estrogen receptor β-DAB2IP signals.

Chiuan-Ren Yeh, Zheng-Yu Ou, Guang-Qian Xiao, Elizabeth Guancial, Shuyuan Yeh

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. The influence of sex hormones on renal cell carcinoma.Therapeutic advances in medical oncology · 2024
    Review
  7. Article
  8. Article
  9. Review
  10. Role of Circular RNA in Kidney-Related Diseases.Frontiers in pharmacology · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. 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

5 authors at 1 institution in 1 country.

Chiuan-Ren YehDepartment of Urology, University of Rochester Medical Center, Rochester, NY 14642, USA.
Zheng-Yu OuDepartment of Urology, University of Rochester Medical Center, Rochester, NY 14642, USA.
Guang-Qian XiaoDepartment of Pathology, University of Rochester Medical Center, Rochester, NY 14642, USA.
Elizabeth GuancialDepartment of Medicine, University of Rochester Medical Center, Rochester, NY 14642, USA.
Shuyuan YehDepartment of Urology, University of Rochester Medical Center, Rochester, NY 14642, USA.
University of Rochester Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous studies indicated the T cells, one of the most common types of immune cells existing in the microenvironment of renal cell carcinoma (RCC), may influence the progression of RCC. The potential linkage of T cells and the estrogen receptor beta (ERβ), a key player to impact RCC progression, however, remains unclear. Our results demonstrate that RCC cells can recruit more T cells than non-malignant kidney cells. Using an in vitro matrigel invasion system, we found infiltrating T cells could promote RCC cells invasion via increasing ERβ expression and transcriptional activity. Mechanism dissection suggested that co-culturing T cells with RCC cells released more T cell attraction factors, including IFN-γ, CCL3 and CCL5, suggesting a positive regulatory feed-back mechanism. Meanwhile, infiltrating T cells may also promote RCC cell invasion via increased ERβ and decreased DAB2IP expressions, and knocking down DAB2IP can then reverse the T cells-promoted RCC cell invasion. Together, our results suggest that infiltrating T cells may promote RCC cell invasion via increasing the RCC cell ERβ expression to inhibit the tumor suppressor DAB2IP signals. Further mechanism dissection showed that co-culturing T cells with RCC cells could produce more IGF-1 and FGF-7, which may enhance the ERβ transcriptional activity. The newly identified relationship between infiltrating T cells/ERβ/DAB2IP signals may provide a novel therapeutic target in the development of agents against RCC.

Indexed as

Paracrine CommunicationCarcinoma, Renal CellCell Line, TumorChemokine CCL3Chemokine CCL5Chemotaxis, LeukocyteCoculture TechniquesEstrogen Receptor betaFibroblast Growth Factor 7Gene Expression Regulation, NeoplasticHumansInsulin-Like Growth Factor IInterferon-gammaKidney NeoplasmsLymphocytes, Tumor-Infiltratingras GTPase-Activating ProteinsCCL3 protein, humanCCL5 protein, humanChemokine CCL3Chemokine CCL5DAB2IP protein, humanESR2 protein, humanEstrogen Receptor betaFGF7 protein, humanFibroblast Growth Factor 7IFNG protein, humanIGF1 protein, humanInsulin-Like Growth Factor IInterferon-gammaras GTPase-Activating ProteinsCD4+ T cellsDAB2IPERβmetastasisRCC

Identifiers

PMID26587829
PMCPMC4792561
OpenAlexW2172432828

What OpenQuestion holds

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LicenceCC BY
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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.