Evidence map›Paper›PMID 28197812›Full record

ArticleAngiogenesis2017

MCPIP1 contributes to clear cell renal cell carcinomas development.

Janusz Ligeza, Paulina Marona, Natalia Gach, Barbara Lipert, Katarzyna Miekus, Waclaw Wilk, Janusz Jaszczynski, Andrzej Stelmach, Agnieszka Loboda, Jozef Dulak and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Angiogenesis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
10.2field-weighted citation impact, top 1% 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

41 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. MCPIP1 modulates the miRNA‒mRNA landscape in keratinocyte carcinomas.Journal of experimental & clinical cancer research : CR · 2024
    Article
  8. Regnase-1 overexpression as a therapeutic approach of Marfan syndrome.Molecular therapy. Methods & clinical development · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Evidence for the Benefits of Melatonin in Cardiovascular Disease.Frontiers in cardiovascular medicine · 2022
    Review
  13. Loss of epidermal MCPIP1 is associated with aggressive squamous cell carcinoma.Journal of experimental & clinical cancer research : CR · 2021
    Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. MCPIP1 RNase and Its Multifaceted Role.International journal of molecular sciences · 2020
    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

13 authors at 2 institutions in 1 country.

Janusz LigezaDepartment of General Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 7 Gronostajowa St, 30-387, Krakow, Poland.
Paulina MaronaDepartment of General Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 7 Gronostajowa St, 30-387, Krakow, Poland.
Natalia GachDepartment of General Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 7 Gronostajowa St, 30-387, Krakow, Poland.
Barbara LipertDepartment of General Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 7 Gronostajowa St, 30-387, Krakow, Poland.
Katarzyna MiekusDepartment of General Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 7 Gronostajowa St, 30-387, Krakow, Poland.
Waclaw WilkCenter of Oncology, Maria Skłodowska-Curie Memorial Institute, Garncarska 11, 31-115, Krakow, Poland.
Janusz JaszczynskiCenter of Oncology, Maria Skłodowska-Curie Memorial Institute, Garncarska 11, 31-115, Krakow, Poland.
Andrzej StelmachCenter of Oncology, Maria Skłodowska-Curie Memorial Institute, Garncarska 11, 31-115, Krakow, Poland.
Agnieszka LobodaDepartment of Medical Biotechnology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Krakow, Poland.
Jozef DulakDepartment of Medical Biotechnology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Krakow, Poland.
Wojciech BranickiDepartment of General Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 7 Gronostajowa St, 30-387, Krakow, Poland.
Janusz RysCenter of Oncology, Maria Skłodowska-Curie Memorial Institute, Garncarska 11, 31-115, Krakow, Poland. z5rys@cyf-kr.edu.pl.
Jolanta JuraDepartment of General Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 7 Gronostajowa St, 30-387, Krakow, Poland. jolanta.jura@uj.edu.pl.ORCID http://orcid.org/0000-0002-0816-3475
Jagiellonian University · PLThe Maria Sklodowska-Curie National Research Institute of Oncology · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monocyte Chemoattractant protein-induced protein 1 (MCPIP1), also known as Regnase-1, is encoded by the ZC3H12a gene, and it mediates inflammatory processes by regulating the stability of transcripts coding for proinflammatory cytokines and controlling activity of transcription factors, such as NF-κB and AP1. We found that MCPIP1 transcript and protein levels are strongly downregulated in clear cell renal cell carcinoma (ccRCC) samples, which were derived from patients surgically treated for renal cancer compared to surrounded normal tissues. Using Caki-1 cells as a model, we analyzed the role of MCPIP1 in cancer development. We showed that MCPIP1 expression depends on the proteasome activity; however, hypoxia and hypoxia inducible factor 2 alfa (HIF2α) are key factors lowering MCPIP1 expression. Furthermore, we found that MCPIP1 negatively regulates HIF1α and HIF2α levels and in the case of the last one, the mechanism is based on the regulation of the half time of transcript coding for HIF2α. Enhanced expression of MCPIP1 in Caki-1 cells results in a downregulation of transcripts encoding VEGFA, GLUT1, and IL-6. Furthermore, MCPIP1 decreases the activity of mTOR and protein kinase B (Akt) in normoxic conditions. Taken together, MCPIP1 contributes to the ccRCC development.

Indexed as

AdultAgedAged, 80 and overBasic Helix-Loop-Helix ProteinsCarcinogenesisCarcinoma, Renal CellCell HypoxiaCell Line, TumorCell SurvivalEndothelial PAS Domain-Containing Protein 1FemaleGlucose Transporter Type 1HumansKidney NeoplasmsLeupeptinsMaleBasic Helix-Loop-Helix Proteinsbenzyloxycarbonylleucyl-leucyl-leucine aldehydeEndothelial PAS Domain-Containing Protein 1Glucose Transporter Type 1LeupeptinsNF-kappa Bp38 Mitogen-Activated Protein KinasesProteasome InhibitorsRibonucleasesRNA, MessengerTranscription FactorsVascular Endothelial Growth Factor AZC3H12A protein, humanAngiogenesisClear cell renal cell carcinoma (ccRCC)HIF1αHIF2αMCPIP1 (Regnase-1)

Identifiers

PMID28197812
PMCPMC5511613
OpenAlexW2588049838

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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.