Evidence map›Paper›PMID 31849836›Full record

ArticleFrontiers in endocrinology2019

The Apoptosis Regulator 14-3-3η and Its Potential as a Therapeutic Target in Pituitary Oncocytoma.

Sida Zhao, Bin Li, Chuzhong Li, Hua Gao, Yazhou Miao, Yue He, Hongyun Wang, Lei Gong, Dan Li, Yazhuo Zhang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

3 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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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

11 authors at 3 institutions in 1 country.

Sida ZhaoCell Biology, Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Bin LiBeijing Tiantan Hospital, Capital Medical University, Beijing, China.
Chuzhong LiCell Biology, Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Hua GaoCell Biology, Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Yazhou MiaoCell Biology, Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Yue HeCell Biology, Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Hongyun WangCell Biology, Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Lei GongCell Biology, Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Dan LiCell Biology, Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Yazhuo ZhangCell Biology, Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Jie FengCell Biology, Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Beijing Institute of Neurosurgery · CNCapital Medical University · CNBeijing Tian Tan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 14-3-3 protein family has attracted much attention in research into the pathogenesis of human tumors because of its involvement in tumorigenesis. In previous studies, we found that 14-3-3η was highly expressed in pituitary oncocytoma. However, the mechanism by which 14-3-3η regulates tumorigenesis in pituitary oncocytoma is unclear. 14-3-3η-binding proteins were investigated in pituitary oncocytoma by immunoprecipitation and proteomic analysis. A total of 443 proteins were identified as 14-3-3η binding proteins. The interactions of 14-3-3η and its binding partners were identified by a network analysis using the STRING database. The network included 433 nodes and 564 edges. PRAS40 (AKT1S1) was a binding protein of 14-3-3η and showed experimental interactions with 14-3-3η in the STRING database. The combined score was 0.407, which suggested a functional link. The 443 binding proteins of 14-3-3η showed enriched molecular signatures in GSEA and GO analysis. PRAS40 (AKT1S1) was enriched in the mTOR signaling pathway. Western blot analysis showed that the relative expression of p-PRAS40 (T246)/PRAS40 was significantly higher in pituitary oncocytoma than in normal pituitary tissues (

Indexed as

14-3-3ηadenoma-pathologyCoIP coimmunoprecipitationmass spectrumpituitaryproteomicstumor proliferation

Identifiers

PMID31849836
PMCPMC6893364
OpenAlexW2991215957

What OpenQuestion holds

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LicenceCC BY
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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.