Evidence map›Paper›PMID 37079115›Full record

ArticleFunctional & integrative genomics2023

Analysis of the regulatory role of miR-34a-5p/PLCD3 in the progression of osteoarthritis.

Pu Ying, Yue Xu, Xiaowei Jiang, Kejie Wang, Yi Xue, Qiang Wang, Wenge Ding, Xiaoyu Dai

Abstract read
PubMed Publisher
In one paragraph

Article in Functional & integrative genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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 2 institutions in 1 country.

Pu YingDepartment of Orthopaedics, Changshu Hospital Affiliated to Nanjing University of Chinese Medicine, Changshu, China.
Yue XuDepartment of Orthopaedics, Changshu Hospital Affiliated to Nanjing University of Chinese Medicine, Changshu, China.
Xiaowei JiangDepartment of Orthopaedics, Changshu Hospital Affiliated to Nanjing University of Chinese Medicine, Changshu, China.
Kejie WangDepartment of Orthopedics, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Yi XueDepartment of Orthopaedics, Changshu Hospital Affiliated to Nanjing University of Chinese Medicine, Changshu, China.
Qiang WangDepartment of Orthopaedics, Changshu Hospital Affiliated to Nanjing University of Chinese Medicine, Changshu, China.
Wenge DingDepartment of Orthopedics, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Xiaoyu DaiDepartment of Orthopedics, The Third Affiliated Hospital of Soochow University, Changzhou, China. dxyiverson3@163.com.
Nanjing University of Chinese Medicine · CNSoochow University · CN

Funding

the Basic Research Project of Changzhou science and Technology Bureau CJ20200112the Project of Changshu Hospital Affiliated to Nanjing University of Chinese Medicine cszyy201910the Youth Project "Science and Education" of Suzhou KJXW2020068
6 · The paper itself

Abstract

Osteoarthritis is a heterogeneous disease with a complex etiology. However, there is no effective treatment strategy at present. The purpose of this study was to explore the miRNA‒mRNA regulatory network and molecular mechanism that regulate the progression of osteoarthritis. In this article, we downloaded datasets (GSE55457, GSE82107, GSE143514 and GSE55235) from Gene Expression Omnibus (GEO) to screen differentially expressed mRNAs in osteoarthritis. Then, through weighted gene coexpression network (WGCNA), functional enrichment, protein‒protein interaction (PPI) network, miRNA‒mRNA coexpression network, ROC curve, and immune infiltration analyses and qPCR, the mRNA PLCD3, which was highly expressed in osteoarthritis and had clinical predictive value, was screened. We found that PLCD3 directly targets miR-34a-5p through DIANA and dual-luciferase experiments. The expression levels of PLCD3 and miR-34a-5p were negatively correlated. In addition, CCK-8 and wound healing assays showed that the miR-34a-5p mimic inhibited hFLS-OA cell proliferation and promoted hFLS-OA cell migration. PLCD3 overexpression showed the opposite trend. Western blotting further found that overexpression of miR-34a-5p reduced the protein expression levels of p-PI3K and p-AKT, while overexpression of PLCD3 showed the opposite trend. In addition, combined with the effect of the PI3K/AKT pathway inhibitor BIO (IC50 = 5.95 μM), the results showed that overexpression of miR-34a-5p increased the inhibitory effects of BIO on p-PI3K and p-AKT protein expression, while overexpression of PLCD3 significantly reversed these inhibitory effects. Overall, the miR-34a-5p/PLCD3 axis may mediate the PI3K/AKT pathway in regulating cartilage homeostasis in synovial osteoarthritis. These data indicate that miR-34a-5p/PLCD3 may be a new prognostic factor in the pathology of synovial osteoarthritis.

Indexed as

MicroRNAsOsteoarthritisApoptosisCell ProliferationHumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRNA, MessengerMicroRNAsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRNA, MessengermiR-34a-5p/PLCD3OsteoarthritisPI3K-Akt pathwayProgressionSynovial fibroblasts

Identifiers

PMID37079115
OpenAlexW4366463545

What OpenQuestion holds

Textmetadata
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.