Evidence map›Paper›PMID 37247031›Full record

ArticleCell and tissue research2023

The histone acetyltransferase Mof regulates Runx2 and Osterix for osteoblast differentiation.

Jianmei Chen, Di Liu, Bo Chen, Yang Yang, Hongying Zhu, Danyang Li, Kun Liu, Lina Zhu, Hongrui Liu, Minqi Li and 2 more

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In one paragraph

Article in Cell and tissue research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 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

12 authors at 3 institutions in 1 country.

Jianmei Chen *Shandong Provincial Key Laboratory of Animal Cells and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, 266237, China.
Di Liu *School of Stomatology, Shandong University, Jinan, 250012, China.
Bo Chen *Qilu Hospital of Shandong University, Jinan, 250012, China.
Yang YangSchool of Pharmacy, Binzhou Medical University, Yantai, 264003, China.
Hongying ZhuShandong Provincial Key Laboratory of Animal Cells and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, 266237, China.
Danyang LiQilu Hospital of Shandong University, Jinan, 250012, China.
Kun LiuShandong Provincial Key Laboratory of Animal Cells and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, 266237, China.
Lina ZhuShandong Provincial Key Laboratory of Animal Cells and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, 266237, China.
Hongrui LiuSchool of Stomatology, Shandong University, Jinan, 250012, China.
Minqi LiSchool of Stomatology, Shandong University, Jinan, 250012, China.
Xu ZhangShandong Provincial Key Laboratory of Animal Cells and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, 266237, China. olive3072002@aliyun.com.
Xiangzhi LiShandong Provincial Key Laboratory of Animal Cells and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, 266237, China. xiangzhi@sdu.edu.cn.ORCID http://orcid.org/0000-0002-2411-2491
Shandong University · CNQilu Hospital of Shandong University · CNBinzhou Medical University · CN

Funding

National Key R&D Program of China 2016YFE0129200National Natural Science Foundation of China 31571321National Natural Science Foundation of China 81601337
6 · The paper itself

Abstract

Osteoblast differentiation is regulated by various transcription factors, signaling molecules, and posttranslational modifiers. The histone acetyltransferase Mof (Kat8) is involved in distinct physiological processes. However, the exact role of Mof in osteoblast differentiation and growth remains unknown. Herein, we demonstrated that Mof expression with histone H4K16 acetylation increased during osteoblast differentiation. Inhibition of Mof by siRNA knockdown or small molecule inhibitor, MG149 which is a potent histone acetyltransferase inhibitor, reduced the expression level and transactivation potential of osteogenic key markers, Runx2 and Osterix, thus inhibiting osteoblast differentiation. Besides, Mof overexpression also enhanced the protein levels of Runx2 and Osterix. Mof could directly bind the promoter region of Runx2/Osterix to potentiate their mRNA levels, possibly through Mof-mediated H4K16ac to facilitate the activation of transcriptional programs. Importantly, Mof physically interacts with Runx2/Osterix for the stimulation of osteoblast differentiation. Yet, Mof knockdown showed indistinguishable effect on cell proliferation or apoptosis in MSCs and preosteoblast cells. Taken together, our results uncover Mof functioning as a novel regulator of osteoblast differentiation via the promotional effects on Runx2/Osterix and rationalize Mof as a potential therapeutic target, like possible application of inhibitor MG149 for the treatment of osteosarcoma or developing specific Mof activator to ameliorate osteoporosis.

Indexed as

OsteogenesisTranscription FactorsAnimalsCell DifferentiationCore Binding Factor Alpha 1 SubunitHistone AcetyltransferasesMiceOsteoblastsSp7 Transcription FactorCore Binding Factor Alpha 1 SubunitHistone AcetyltransferasesKat8 protein, mouseRunx2 protein, mouseSp7 protein, mouseSp7 Transcription FactorTranscription FactorsExpressionMofOsteoblast DifferentiationOsterixRunx2

Identifiers

PMID37247031
OpenAlexW4378640246

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.