Evidence map›Paper›PMID 22227519›Full record

ArticleThe EMBO journal2012

Ablation of Rassf2 induces bone defects and subsequent haematopoietic anomalies in mice.

Hoogeun Song, Hyunsoo Kim, Kyunghee Lee, Da-Hye Lee, Tae-Shin Kim, Ji Yun Song, Dongjun Lee, Dongwook Choi, Chang-Yong Ko, Han-Sung Kim and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.7field-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

24 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. The Role of Aryl Hydrocarbon Receptor in Bone Biology.International journal of tryptophan research : IJTR · 2024
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Tumor suppressor C-RASSF proteins.Cellular and molecular life sciences : CMLS · 2018
    Review
  12. Article
  13. Article
  14. Ras signaling through RASSF proteins.Seminars in cell & developmental biology · 2016
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

16 authors at 7 institutions in 2 countries.

Hoogeun SongDepartment of Biological Sciences, National Creative Research Initiatives Center, Graduate School of Nanoscience and Technology, Korea Advanced Institute of Science and Technology, Daejeon, Korea.
Hyunsoo Kim
Kyunghee Lee
Da-Hye Lee
Tae-Shin Kim
Ji Yun Song
Dongjun Lee
Dongwook Choi
Chang-Yong Ko
Han-Sung Kim
Hong-In Shin
Juhyun Choi
Heedong Park
Chankyu Park
Daewon Jeong
Dae-Sik Lim
Korea Advanced Institute of Science and Technology · KRCreative Research · GBKorea Development Institute · KRYeungnam University Medical Center · KRYonsei University · KRKyungpook National University · KRYeungnam University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RASSF2 belongs to the Ras-association domain family (RASSF) of proteins, which may be involved in the Hippo signalling pathway. However, the role of RASSF2 in vivo is unknown. Here, we show that Rassf2 knockout mice manifest a multisystemic phenotype including haematopoietic anomalies and defects in bone remodelling. Bone marrow (BM) transplantation showed that Rassf2(-/-) BM cells had a normal haematopoietic reconstitution activity, indicating no intrinsic haematopoietic defects. Notably, in vitro differentiation studies revealed that ablation of Rassf2 suppressed osteoblastogenesis but promoted osteoclastogenesis. Co-culture experiments showed that an intrinsic defect in osteoblast differentiation from Rassf2(-/-) osteoblast precursors likely leads to both haematopoiesis and osteoclast defects in Rassf2(-/-) mice. Moreover, Rassf2 deficiency resulted in hyperactivation of nuclear factor (NF)-κB during both osteoclast and osteoblast differentiation. RASSF2 associated with IκB kinase (IKK) α and β forms, and suppressed IKK activity. Introduction of either RASSF2 or a dominant-negative form of IKK into Rassf2(-/-) osteoclast or osteoblast precursors inhibited NF-κB hyperactivation and normalized osteoclast and osteoblast differentiation. These observations indicate that RASSF2 regulates osteoblast and osteoclast differentiation by inhibiting NF-κB signalling.

Indexed as

HematopoiesisAnimalsBone ResorptionCell DifferentiationCell ProliferationI-kappa B KinaseMiceMice, KnockoutNF-kappa BOsteoblastsOsteoclastsOsteogenesisProtein BindingProtein Interaction MappingTumor Suppressor ProteinsI-kappa B KinaseNF-kappa BRASSF2 protein, mouseTumor Suppressor Proteins

Identifiers

PMID22227519
PMCPMC3297990
OpenAlexW2163667557

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.