Evidence map›Paper›PMID 30274213›Full record

ArticleToxins2018

The Effects of Autophagy and PI3K/AKT/m-TOR Signaling Pathway on the Cell-Cycle Arrest of Rats Primary Sertoli Cells Induced by Zearalenone.

Bing-Jie Wang, Wang-Long Zheng, Nan-Nan Feng, Tao Wang, Hui Zou, Jian-Hong Gu, Yan Yuan, Xue-Zhong Liu, Zong-Ping Liu, Jian-Chun Bian

Open access · goldAbstract read
In one paragraph

Article in Toxins, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 71 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

10 authors at 1 institution in 1 country.

Bing-Jie WangCollege of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China. wangbingjieyzh@outlook.com.
Wang-Long ZhengCollege of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China. wanglongzheng@vet.k-state.edu.
Nan-Nan FengCollege of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China. fengnannan8@outlook.com.
Tao WangCollege of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China. wtao6550@yzu.edu.cn.
Hui ZouCollege of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China. zouhui@yzu.edu.cn.
Jian-Hong GuCollege of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China. jhgu@yzu.edu.cn.
Yan YuanCollege of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China. yuanyan@yzu.edu.cn.
Xue-Zhong LiuCollege of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China. Liuxuezhong68@yzu.edu.cn.
Zong-Ping LiuCollege of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China. liuzongping@yzu.edu.cn.
Jian-Chun BianCollege of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China. jcbian@yzu.edu.cn.
Yangzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A high concentration of Zearalenone (ZEA) will perturb the differentiation of germ cells, and induce a death of germ cells, but the toxic mechanism and molecular mechanism remain unclear. The Sertoli cells (SCs) play an irreplaceable role in spermatogenesis. In order to explore the potential mechanism of ZEA male reproductive toxicity, we studied the effects of ZEA on cell proliferation, cell-cycle distribution, cell-cycle-related proteins and autophagy-related pathway the PI3K/Akt/mTOR signaling in primary cultured rats SCs, and the effects of autophagy and PI3K/AKT/m TOR signaling pathway on the SCs cell-cycle arrest induced by ZEA treated with the autophagy promoter RAPA, autophagy inhibitor CQ, and the PI3K inhibitor LY294002, respectively. The data revealed that ZEA could inhibit the proliferation of SCs by arresting the cell cycle in the G2/M phase and trigger the autophagy via inhibiting the PI3K/Akt/m TOR signaling pathway. Promoting or inhibiting the level of autophagy could either augment or reverse the arrest of cell cycle. And it was regulated by PI3K/Akt/m TOR signaling pathway. Taken together, this study provides evidence that autophagy and PI3K/Akt/m TOR signaling pathway are involved in regulating rats primary SCs cell-cycle arrest due to ZEA in vitro. To some extent, ZEA-induced autophagy plays a protective role in this process.

Indexed as

AnimalsAutophagyCell Cycle CheckpointsCells, CulturedMalePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRats, WistarSertoli CellsSignal TransductionTOR Serine-Threonine KinasesZearalenonemTOR protein, ratPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesZearalenoneAutophagycell cycleG2/M arrestPI3K/Akt/m TOR signalingSertoli cells (SCs)Zearalenone (ZEA)

Identifiers

PMID30274213
PMCPMC6215106
OpenAlexW2893781673

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.