Evidence map›Paper›PMID 33569722›Full record

ArticleJournal of bone and mineral metabolism2021

LncPVT1 promotes cartilage degradation in diabetic OA mice by downregulating miR-146a and activating TGF-β/SMAD4 signaling.

Yan-Zhi Wang, Yao-Li, Sheng-Kai Liang, Luo-Bin Ding, Feng-Li, Jian Guan, Hua-Jun Wang

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In one paragraph

Article in Journal of bone and mineral metabolism, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Interaction between diabetes and osteoporosis: imbalance between inflammation and bone remodeling.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2025
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  14. MiR-19b-3p Attenuates Chondrocytes Injury by Inhibiting MAPK/NF-Κb Axis via Targeting SOCS1.Evidence-based complementary and alternative medicine : eCAM · 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

7 authors at 1 institution in 1 country.

Yan-Zhi WangDepartment of Orthopedic Surgery, Third Hospital of Shijiazhuang, ChangAn District, , Shijiazhuang, 050011, HeBei, China.
Yao-LiDepartment of Orthopedic Surgery, Third Hospital of Shijiazhuang, ChangAn District, , Shijiazhuang, 050011, HeBei, China.
Sheng-Kai LiangDepartment of Orthopedic Surgery, Third Hospital of Shijiazhuang, ChangAn District, , Shijiazhuang, 050011, HeBei, China.
Luo-Bin DingDepartment of Orthopedic Surgery, Third Hospital of Shijiazhuang, ChangAn District, , Shijiazhuang, 050011, HeBei, China.
Feng-LiDepartment of Orthopedic Surgery, Third Hospital of Shijiazhuang, ChangAn District, , Shijiazhuang, 050011, HeBei, China.
Jian GuanDepartment of Orthopedic Surgery, Third Hospital of Shijiazhuang, ChangAn District, , Shijiazhuang, 050011, HeBei, China. gjortho@outlook.com.
Hua-Jun WangDepartment of Orthopedic Surgery and Sports Medicine Center, The First Affiliated Hospital of Jinan University, Road West No. 613, Huang-Pu, Guangzhou, 510632, GuangDong, China. whjortho@hotmail.com.
First Affiliated Hospital of Jinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTo investigate the role of LncRNA PVT1 (plasmacytoma variant translocation 1) in hyperglycemia-triggered cartilage damage using the diabetic osteoarthritis (OA) mice model. MATERIALS AND

methodsStreptozotocin (STZ) was used to induce mouse diabetes. Knee OA model was induced through transection of anterior cruciate ligament (ACLT). Severity of arthritis was assessed histologically by Safranin O-Fast Green Staining using Mankin Scores. LncRNA PVT1 and miR-146a were detected by real-time polymerase chain reaction (PCR) in cartilage tissue. Moreover, the interaction among PVT1, miR-146a, and SMAD4 was examined by luciferase reporter assays. Mice were injected intra-articularly with ad-siRNA-PVT1 and ad-siRNA scramble control. Articular concentrations of TNF-α, IL-1, IL-6 and TGF-β1 were determined using enzyme-linked immunosorbent assay. Levels of type II Collagen (COL2A1), TGF-β1, p-SMAD2, SMAD2, p-SMAD3, SMAD3, SMAD4 and nuclear SMAD4 were detected by western blot analysis.

resultsPVT1 expression was significantly increased, whereas miR-146a was markedly decreased in diabetic OA mice than in non-diabetic OA and control. Increased PVT1 expression in diabetic OA mice was significantly associated with Mankin score and reduced miR-146a as well as Collagen alpha-1(II) (COL2A1) expressions. In vivo, intra-articular injection of ad-siRNA-PVT1 efficiently increased miR-146a and COL2A1 expressions, alleviated joint inflammation, decreased the expression of pro-inflammatory mediators, and suppressed TGF-β/SMAD4 pathway in diabetic OA mice.

conclusionsOur results demonstrate LncRNA PVT1 is involved in cartilage degradation in diabetic OA and correlated with disease severity. Efficiency of ad-siRNA-PVT1 in controlling joint inflammation in diabetic OA mice is associated with the suppression of the expression of miR-146a, pro-inflammatory cytokines and activation of TGF-β/SMAD4 pathway.

Indexed as

Down-RegulationAdenoviridaeAnimalsBase SequenceCartilage, ArticularCollagen Type IIDiabetes Mellitus, ExperimentalHEK293 CellsHumansHyperglycemiaMatrix Metalloproteinase 13Matrix Metalloproteinase 3MiceMice, Inbred C57BLMicroRNAsOsteoarthritisCol2a1 protein, mouseCollagen Type IIMatrix Metalloproteinase 13Matrix Metalloproteinase 3MicroRNAsMirn146 microRNA, mousePVT1 long-non-coding RNA, mouseRNA, Long NoncodingRNA, Small InterferingSmad4 ProteinTransforming Growth Factor betaTransforming Growth Factor beta1Tumor Necrosis Factor-alphaDiabetic osteoarthritisMiR-146PVT1TGF-β/SMAD signaling

Identifiers

PMID33569722
OpenAlexW3127509739

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.