Evidence map›Paper›PMID 24403568›Full record

ArticleJournal of molecular endocrinology2014

PCP4: a regulator of aldosterone synthesis in human adrenocortical tissues.

Saulo J A Felizola, Yasuhiro Nakamura, Yoshikiyo Ono, Kanako Kitamura, Kumi Kikuchi, Yoshiaki Onodera, Kazue Ise, Kei Takase, Akira Sugawara, Namita Hattangady and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of molecular endocrinology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

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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 3 institutions in 2 countries.

Saulo J A FelizolaDepartment of Pathology, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8575, Japan Division of Nephrology, Endocrinology and Vascular Medicine, Tohoku University Hospital, Sendai, Japan Departments of Diagnostic Radiology Molecular Endocrinology, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8575, Japan Department of Physiology and Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Yasuhiro Nakamura
Yoshikiyo Ono
Kanako Kitamura
Kumi Kikuchi
Yoshiaki Onodera
Kazue Ise
Kei Takase
Akira Sugawara
Namita Hattangady
William E Rainey
Fumitoshi Satoh
Hironobu Sasano
Tohoku University · JPTohoku University Hospital · JPUniversity of Michigan–Ann Arbor · US

Funding

Molecular Mechanisms of AdrenarcheR01DK069950 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RAINEY, WILLIAM E · 2005 to 2019
$4.4M
NIDDK NIH HHS R01 DK069950
6 · The paper itself

Abstract

Purkinje cell protein 4 (PCP4) is a calmodulin (CaM)-binding protein that accelerates calcium association and dissociation with CaM. It has been previously detected in aldosterone-producing adenomas (APA), but details on its expression and function in adrenocortical tissues have remained unknown. Therefore, we performed the immunohistochemical analysis of PCP4 in the following tissues: normal adrenal (NA; n=15), APA (n=15), cortisol-producing adenomas (n=15), and idiopathic hyperaldosteronism cases (IHA; n=5). APA samples (n=45) were also submitted to quantitative RT-PCR of PCP4, CYP11B1, and CYP11B2, as well as DNA sequencing for KCNJ5 mutations. Transient transfection analysis using PCP4 siRNA was also performed in H295R adrenocortical carcinoma cells, following ELISA analysis, and CYP11B2 luciferase assays were also performed after PCP4 vector transfection in order to study the regulation of PCP4 protein expression. In our findings, PCP4 immunoreactivity was predominantly detected in APA and in the zona glomerulosa of NA and IHA. In APA, the mRNA levels of PCP4 were significantly correlated with those of CYP11B2 (P<0.0001) and were significantly higher in cases with KCNJ5 mutation than WT (P=0.005). Following PCP4 vector transfection, CYP11B2 luciferase reporter activity was significantly higher than controls in the presence of angiotensin-II. Knockdown of PCP4 resulted in a significant decrease in CYP11B2 mRNA levels (P=0.012) and aldosterone production (P=0.011). Our results indicate that PCP4 is a regulator of aldosterone production in normal, hyperplastic, and neoplastic human adrenocortical cells.

Indexed as

AdenomaAdrenal CortexAdrenal Cortex NeoplasmsAldosteroneAngiotensin IIBlotting, WesternCell LineColforsinCytochrome P-450 CYP11B2DNAEnzyme AssaysEnzyme-Linked Immunosorbent AssayGene Expression Regulation, NeoplasticHumansImmunohistochemistryLuciferasesAldosteroneAngiotensin IIColforsinCytochrome P-450 CYP11B2DNALuciferasesNerve Tissue ProteinsPCP4 protein, humanRNA, Small InterferingSteroid 11-beta-Hydroxylaseadrenal cortexaldosteronecalmodulin (CaM)CYP11B2Purkinje cell protein 4 (PCP4)

Identifiers

PMID24403568
PMCPMC4103644
OpenAlexW2114892346

What OpenQuestion holds

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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.