Evidence map›Paper›PMID 33988757›Full record

ArticleJournal of bone and mineral metabolism2021

FSH modulated cartilage ECM metabolism by targeting the PKA/CREB/SOX9 pathway.

Mengqi Zhang, Yan Wang, Zhikun Huan, Yaping Liu, Wenwen Zhang, Dehuan Kong, Lei Kong, Jin Xu

Abstract read
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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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Independent Skeletal Actions of Pituitary Hormones.Endocrinology and metabolism (Seoul, Korea) · 2022
    Article
  9. Article
  10. Article
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 4 institutions in 1 country.

Mengqi ZhangSchool of Medicine, Shandong University, jinan, 250021, shandong, China.
Yan WangSchool of Medicine, Shandong University, jinan, 250021, shandong, China.
Zhikun HuanSchool of Medicine, Shandong University, jinan, 250021, shandong, China.
Yaping LiuSchool of Medicine, Shandong University, jinan, 250021, shandong, China.
Wenwen ZhangSchool of Medicine, Shandong University, jinan, 250021, shandong, China.
Dehuan KongDepartment of Geriatrics, Taian City Central Hospital, Taian, Shandong, China.
Lei Kong *School of Medicine, Shandong University, jinan, 250021, shandong, China. lgkonglei@hotmail.com.
Jin Xu *School of Medicine, Shandong University, jinan, 250021, shandong, China. xujin267903@163.com.
Shandong University · CNShandong Provincial Hospital · CNShandong First Medical University · CNTaian City Central Hospital · CN

Funding

Key Technology Research and Development Program of Shandong 2016GGH3118Key Technology Research and Development Program of Shandong 2016 GSF201025National Natural Science Foundation of China Grant no. 81370892
6 · The paper itself

Abstract

introductionOsteoarthritis (OA) is a common joint disease characterized by articular cartilage degeneration. The prevalence of OA is higher among women than men, and this prevalence is closely related to menopause. The classic view assumes that the underlying mechanism of postmenopausal OA is attributed to declining estrogen levels. Although follicle-stimulating hormone (FSH) levels become elevated in parallel, the effects of FSH on OA have been poorly explored. The present study aimed to study the effect of FSH on cartilage metabolism.

methodsChondrocyte-like ATDC5 cells were treated with recombinant FSH protein. Then the cell viability was measured using cell counting kit-8 assay. Expressions of crucial factors involved in the extracellular matrix (ECM) metabolic and PKA-CREB-SOX9 pathway were analyzed by western blot, RT-qPCR, and immunofluorescence staining. Intracellular cAMP levels were assessed by ELISA assay. Experimental OA in mice was induced by destabilization of the medial meniscus (DMM) surgery. Adeno-associated virus expressing shRNA against FSHR (AAV-shFSHR) was intra-articular (IA) injected into the OA model animals to specifically knock down FHSR in cartilage. Histological staining and OARSI scores were used to assess the efficacy of AAV-shFSHR injections.

resultsWe found that FSH down-regulated the expression of ECM-related proteins in chondrocyte-like ATDC5 cells. The underlying mechanism is probably associated with regulating PKA/CREB/SOX9 pathway. Besides, blocking FSH signaling via shRNA-mediated downregulation of FSHR in joint tissues effectively delayed the development of posttraumatic OA in mice.

conclusionsOur results collectively indicated that FSH plays an essential role in the pathogenesis of OA and acts as a crucial mediator.

Indexed as

Cartilage, ArticularOsteoarthritisAnimalsChondrocytesExtracellular MatrixFemaleFollicle Stimulating HormoneMiceMice, Inbred C57BLFollicle Stimulating HormoneExtracellular matrixFollicle-stimulating hormoneOsteoarthritisPKA

Identifiers

PMID33988757
OpenAlexW3160273816

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.