Evidence map›Paper›PMID 29115419›Full record

ArticleMolecular medicine reports2018

Effect of β‑ecdysterone on glucocorticoid‑induced apoptosis and autophagy in osteoblasts.

Yang-Hua Tang, Zhen-Shuang Yue, Guo-Song Li, Lin-Ru Zeng, Da-Wei Xin, Zhong-Qing Hu, Can-Da Xu

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

  1. mClinical and translational medicine · 2026
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  19. The Effects of Biomaterial Implant Wear Debris on Osteoblasts.Frontiers in cell and developmental biology · 2020
    Review
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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

7 authors.

Yang-Hua TangDepartment of Orthopedics, Xiaoshan TCM Hospital, Hangzhou, Zhejiang 311201, P.R. China.
Zhen-Shuang YueDepartment of Orthopedics, Xiaoshan TCM Hospital, Hangzhou, Zhejiang 311201, P.R. China.
Guo-Song LiDepartment of Anesthesiology, Xiaoshan TCM Hospital, Hangzhou, Zhejiang 311201, P.R. China.
Lin-Ru ZengDepartment of Orthopedics, Xiaoshan TCM Hospital, Hangzhou, Zhejiang 311201, P.R. China.
Da-Wei XinDepartment of Orthopedics, Xiaoshan TCM Hospital, Hangzhou, Zhejiang 311201, P.R. China.
Zhong-Qing HuDepartment of Orthopedics, Xiaoshan TCM Hospital, Hangzhou, Zhejiang 311201, P.R. China.
Can-Da XuDepartment of Orthopedics, Xiaoshan TCM Hospital, Hangzhou, Zhejiang 311201, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study was to investigate the effect of glucocorticoids in osteoblasts and to examine the role of β‑ecdysterone in the pathogenesis of glucocorticoid‑induced osteoporosis. Osteoblasts were induced from bone marrow mesenchymal stem cells, which were isolated from C57BL/6 mice. Cell viability and apoptosis of osteoblasts were measured by Cell Counting Kit‑8 and flow cytometry analysis, respectively. The expression of related genes and proteins was measured by reverse transcription quantitative polymerase chain reaction and western blot analysis respectively. Dose‑dependent decreases in the cell proliferation and differentiation were observed in dexamethasone (Dex)‑treated osteoblasts, evidenced by downregulation in the activity of alkaline phosphatasedecreased expression levels of Runt‑related transcription factor 2 and osteocalcin, and upregulated expression of RANK ligand. Dex also induced apoptosis and inhibited autophagy of osteoblasts, evidenced by upregulated B‑cell lymphoma 2 (Bcl‑2)‑associated X protein/Bcl‑2 ratio and the activation of mammalian target of rapamycin (mTOR), and decreased expression levels of Beclin‑1, autophagy protein 5 and microtubule‑associated protein 1 light chain 3 II. The effects on cell proliferation, apoptosis and autophagy induced by Dex were reversed by β‑ecdysterone in a dose‑dependent manner. Therefore, β‑ecdysterone may be a promising candidate drug for the treatment of osteoporosis through inducing osteoblast autophagic activity by inactivating mTOR.

Indexed as

AnimalsApoptosisAutophagyCell DifferentiationEcdysteroneGlucocorticoidsMaleMesenchymal Stem CellsMiceOsteoblastsEcdysteroneGlucocorticoids

Identifiers

PMID29115419
PMCPMC5780097
OpenAlexW2766251313

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.