Evidence map›Paper›PMID 35027542›Full record

ArticleCell death & disease2022

ZC3H15 promotes glioblastoma progression through regulating EGFR stability.

Jianbing Hou, Minghao Xu, Hongyu Gu, Dakun Pei, Yudong Liu, Pan Huang, Hongbo Chang, Hongjuan Cui

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

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  18. RAI14 Promotes Melanoma Progression by Regulating the FBXO32/c-MYC Pathway.International journal of molecular sciences · 2022
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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

8 authors at 1 institution in 1 country.

Jianbing HouState Key Laboratory of Silkworm Genome Biology, Southwest University, 400716, Chongqing, China.
Minghao XuState Key Laboratory of Silkworm Genome Biology, Southwest University, 400716, Chongqing, China.ORCID 0000-0003-0535-8231
Hongyu GuState Key Laboratory of Silkworm Genome Biology, Southwest University, 400716, Chongqing, China.
Dakun PeiState Key Laboratory of Silkworm Genome Biology, Southwest University, 400716, Chongqing, China.
Yudong LiuState Key Laboratory of Silkworm Genome Biology, Southwest University, 400716, Chongqing, China.
Pan HuangState Key Laboratory of Silkworm Genome Biology, Southwest University, 400716, Chongqing, China.
Hongbo ChangState Key Laboratory of Silkworm Genome Biology, Southwest University, 400716, Chongqing, China.
Hongjuan CuiState Key Laboratory of Silkworm Genome Biology, Southwest University, 400716, Chongqing, China. hongjuan.cui@gmail.com.ORCID 0000-0003-1178-1570
Southwest University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zinc finger CCCH-type containing 15 (ZC3H15), a highly conserved protein involved in several cellular processes, which was responsible for tumorigenesis and may be a promising marker in myeloid leukemia (AML) and hepatocellular carcinoma (HCC). However, little is known about the biological significance and molecular mechanisms of ZC3H15 in GBM. In this study, we revealed that ZC3H15 was overexpressed in GBM and high ZC3H15 expression was associated with poor survival of patients with GBM. We found that ZC3H15 promoted the proliferation, migration, invasion, and tumorigenesis of GBM cells by activating the EGFR signaling pathway. We also revealed that ZC3H15 reduced EGFR ubiquitination, which was responsible for EGFR protein stabilization. In addition, we demonstrated that ZC3H15 inhibited the transcription of CBL, which was an E3 ubiquitin ligase for EGFR proteasomal degradation. And silencing of CBL could partly abrogate the inhibitory effects on cell proliferation, migration, and invasion of GBM cells induced by ZC3H15 knockdown. Thus, our research revealed the important roles of ZC3H15 in GBM development and provided a brand-new insight for improving the treatment of GBMs.

Indexed as

Brain NeoplasmsCarcinoma, HepatocellularGlioblastomaLiver NeoplasmsCarcinogenesisCell Line, TumorCell MovementCell ProliferationCell Transformation, NeoplasticErbB ReceptorsGene Expression Regulation, NeoplasticHumansRNA-Binding ProteinsEGFR protein, humanErbB ReceptorsRNA-Binding ProteinsZC3H15 protein, human

Identifiers

PMID35027542
PMCPMC8758739
OpenAlexW4206814225

What OpenQuestion holds

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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.