Evidence map›Paper›PMID 26697291›Full record

ArticleResults in immunology2015

A focused Real Time PCR strategy to determine GILZ expression in mouse tissues.

Luigi Cari, Erika Ricci, Marco Gentili, Maria Grazia Petrillo, Emira Ayroldi, Simona Ronchetti, Giuseppe Nocentini, Carlo Riccardi

Open access · hybridAbstract read
In one paragraph

Article in Results in immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Association of GILZ with MUC2, TLR2, and TLR4 in Inflammatory Bowel Disease.International journal of molecular sciences · 2023
    Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. 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

8 authors at 1 institution in 1 country.

Luigi CariDepartment of Medicine, Section of Pharmacology, University of Perugia Medical School, P.le L. Severi 1, 06132 Perugia, Italy.
Erika RicciDepartment of Medicine, Section of Pharmacology, University of Perugia Medical School, P.le L. Severi 1, 06132 Perugia, Italy.
Marco GentiliDepartment of Medicine, Section of Pharmacology, University of Perugia Medical School, P.le L. Severi 1, 06132 Perugia, Italy.
Maria Grazia PetrilloDepartment of Medicine, Section of Pharmacology, University of Perugia Medical School, P.le L. Severi 1, 06132 Perugia, Italy.
Emira AyroldiDepartment of Medicine, Section of Pharmacology, University of Perugia Medical School, P.le L. Severi 1, 06132 Perugia, Italy.
Simona RonchettiDepartment of Medicine, Section of Pharmacology, University of Perugia Medical School, P.le L. Severi 1, 06132 Perugia, Italy.
Giuseppe NocentiniDepartment of Medicine, Section of Pharmacology, University of Perugia Medical School, P.le L. Severi 1, 06132 Perugia, Italy.
Carlo RiccardiDepartment of Medicine, Section of Pharmacology, University of Perugia Medical School, P.le L. Severi 1, 06132 Perugia, Italy.
University of Perugia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glucocorticoid-Induced Leucine Zipper (GILZ) is a glucocorticoid-inducible gene that mediates glucocorticoid anti-inflammatory effects. GILZ and the isoform L-GILZ are expressed in a variety of cell types, especially of hematopoietic origin, including macrophages, lymphocytes and epithelial cells, and strongly upregulated upon glucocorticoid treatment. A quantitative analysis of GILZ expression in mouse tissues is technically difficult to perform because of the presence of a pseudogene and the high homology of GILZ gene with other genes of TSC22 family. We here propose specific primer pairs to be used in Real Time PCR to avoid unwanted amplification of GILZ pseudogene and TSC-22 family member d1iso3. These primer pairs were used to determine GILZ and L-GILZ expression, in either untreated or in vivo and in vitro dexamethasone-treated tissues. Results indicate that GILZ and L-GILZ are upregulated by glucocorticoids, being GILZ more sensitive to glucocorticoid induction than L-GILZ, but they are differently expressed in all examined tissues, confirming a different role in specific cells. An inappropriate primer pair amplified also GILZ pseudogene and TSC22d1iso3, thus producing misleading results. This quantitative evaluation may be used to better characterize the role of GILZ and L-GILZ in mice and may be translated to humans.

Indexed as

GILZGILZ pseudogeneGlucocorticoidsL-GILZReal Time PCRTSC22d1

Identifiers

PMID26697291
PMCPMC4664734
OpenAlexW2192253841

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.