Evidence map›Paper›PMID 35565907›Full record

ArticleNutrients2022

Novel Soy Peptide CBP: Stimulation of Osteoblast Differentiation via TβRI-p38-MAPK-Depending RUNX2 Activation.

Kuaitian Wang, Xiao Kong, Mengdi Du, Wei Yu, Zhenhua Wang, Bo Xu, Jianrong Yang, Jingru Xu, Zhili Liu, Yongqiang Cheng and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 30 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

11 authors at 2 institutions in 1 country.

Kuaitian WangCollege of Life Science, Yantai University, Yantai 264000, China.
Xiao KongCollege of Life Science, Yantai University, Yantai 264000, China.
Mengdi DuCollege of Life Science, Yantai University, Yantai 264000, China.
Wei YuCollege of Life Science, Yantai University, Yantai 264000, China.
Zhenhua WangCollege of Life Science, Yantai University, Yantai 264000, China.
Bo XuCollege of Life Science, Yantai University, Yantai 264000, China.
Jianrong YangCollege of Life Science, Yantai University, Yantai 264000, China.
Jingru XuCollege of Life Science, Yantai University, Yantai 264000, China.
Zhili LiuCollege of Life Science, Yantai University, Yantai 264000, China.
Yongqiang ChengBeijing Key Laboratory of Functional Food from Plant Resources, College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 100083, China.
Jing GanCollege of Life Science, Yantai University, Yantai 264000, China.
Yantai University · CNChina Agricultural University · CN

Funding

National Science Foundation of China 32172161
6 · The paper itself

Abstract

DEDEQIPSHPPR, the calcium-binding peptide (CBP) identified in soy yogurt, was proven to be a potential cofactor in osteoporosis prevention in our previous study, but the mechanism was unknown. In this study, the activity of alkaline phosphatase (ALP) and osteocalcin (OCN), the regulation of RUNX2, and the expression of TβRI were investigated to elucidate the underlying mechanism. The results show that CBP upregulated ALP activity and OCN concentration and increased the expression of RUNX2 and the activation of the MAPK signaling pathway. Similarly, the expression of osteogenesis-related genes in osteoblasts also increased upon CBP treatment. Moreover, the CBP-induced enhancement of ALP activity and phosphorylation levels in the p38 pathway was inhibited by treatment with a p38 inhibitor (SB203538) and TβRI inhibitor (SB431542), respectively, suggesting that p38 and TβRI were involved in the osteogenic action. Based on the signaling pathways, the intracellular calcium concentration was significantly elevated by CBP, which was correlated with the increased behavioral functions and the relative fluorescence intensity of the bone mass. These findings suggest that CBP stimulates osteoblast differentiation and bone mineralization through the activation of RUNX2 via mechanisms related to the TβRI-p38-MAPK signaling pathways, further highlighting CBP's important potential for treating osteoporosis.

Indexed as

Core Binding Factor Alpha 1 SubunitOsteoporosisAlkaline PhosphataseCalciumCell DifferentiationHumansOsteoblastsOsteocalcinOsteogenesisp38 Mitogen-Activated Protein KinasesPeptidesAlkaline PhosphataseCalciumCore Binding Factor Alpha 1 SubunitOsteocalcinp38 Mitogen-Activated Protein KinasesPeptidesRUNX2 protein, humanbone remodelingdifferentiationosteoblastp38-MAPKRUNX2soy peptide CBP

Identifiers

PMID35565907
PMCPMC9105634
OpenAlexW4229056282

What OpenQuestion holds

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LicenceCC BY
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.