Evidence map›Paper›PMID 34350720›Full record

ArticleJournal of cellular and molecular medicine2021

Fluid shear stress regulates osteoblast proliferation and apoptosis via the lncRNA TUG1/miR-34a/FGFR1 axis.

Xingwen Wang, Jinwen He, Hong Wang, Dacheng Zhao, Bin Geng, Shenghong Wang, Jiangdong An, Cuifang Wang, Hua Han, Yayi Xia

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 36 citations in OpenAlex.

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  14. Noncoding RNAs: the crucial role of programmed cell death in osteoporosis.Frontiers in cell and developmental biology · 2024
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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.

Xingwen WangDepartment of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Jinwen HeDepartment of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Hong WangDepartment of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Dacheng ZhaoDepartment of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Bin GengDepartment of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Shenghong WangDepartment of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Jiangdong AnDepartment of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Cuifang WangDepartment of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Hua HanDepartment of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Yayi XiaDepartment of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, Gansu, China.ORCID 0000-0002-3776-4560
Lanzhou University Second Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

LncRNAs and microRNAs play critical roles in osteoblast differentiation and bone formation. However, their exact roles in osteoblasts under fluid shear stress (FSS) and the possible mechanisms remain unclear. The aim of this study was to explore whether and how miR-34a regulates osteoblast proliferation and apoptosis under FSS. In this study, FSS down-regulated miR-34a levels of MC3T3-E1 cells. MiR-34a up-regulation attenuated FSS-induced promotion of proliferation and suppression of apoptosis. Luciferase reporter assay revealed that miR-34a directly targeted FGFR1. Moreover, miR-34a regulated osteoblast proliferation and apoptosis via FGFR1. Further, we validated that lncRNA TUG1 acted as a competing endogenous RNA (ceRNA) to interact with miR-34a and up-regulate FGFR1 protein expression. Furthermore, lncRNA TUG1 could promote proliferation and inhibit apoptosis. Taken together, our study revealed the key role of the lncRNA TUG1/miR-34a/FGFR1 axis in FSS-regulated osteoblast proliferation and apoptosis and may provide potential therapeutic targets for osteoporosis.

Indexed as

OsteoblastsAnimalsCell DifferentiationCell ProliferationHEK293 CellsHumansMiceMicroRNAsReceptor, Fibroblast Growth Factor, Type 1RNA, Long NoncodingStress, MechanicalFgfr1 protein, mouselong non-coding RNA TUG1, mouseMicroRNAsMIRN34a microRNA, mouseReceptor, Fibroblast Growth Factor, Type 1RNA, Long NoncodingapoptosisFGFR1fluid shear stresslncRNA TUG1miR-34aosteoblastproliferation

Identifiers

PMID34350720
PMCPMC8435422
OpenAlexW3190371491

What OpenQuestion holds

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LicenceCC BY
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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.