Evidence map›Paper›PMID 30349003›Full record

ArticleCell death & disease2018

Depletion of MOB1A/B causes intestinal epithelial degeneration by suppressing Wnt activity and activating BMP/TGF-β signaling.

June Sung Bae, Yoon Jeon, Sun Mi Kim, Ji Yun Jang, Mi Kyung Park, In-Hoo Kim, Deog Su Hwang, Dae-Sik Lim, Ho Lee

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Hippo-Yap/Taz signaling: Complex network interactions and impact in epithelial cell behavior.Wiley interdisciplinary reviews. Developmental biology · 2020
    Review
  11. Stem Cell Signaling Pathways in the Small Intestine.International journal of molecular sciences · 2020
    Review
  12. Role of Hippo-YAP1/TAZ pathway and its crosstalk in cardiac biology.International journal of biological sciences · 2020
    Review
  13. Review
  14. Article
  15. Review
  16. 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

9 authors at 4 institutions in 2 countries.

June Sung BaeResearch Institute, National Cancer Center, Goyang, Gyeonggi, 10408, Republic of Korea.
Yoon JeonResearch Institute, National Cancer Center, Goyang, Gyeonggi, 10408, Republic of Korea.
Sun Mi KimGraduate School of Cancer Science and Policy, National Cancer Center, Goyang, Gyeonggi, 10408, Republic of Korea.ORCID http://orcid.org/0000-0002-6918-2100
Ji Yun JangResearch Institute, National Cancer Center, Goyang, Gyeonggi, 10408, Republic of Korea.
Mi Kyung ParkGraduate School of Cancer Science and Policy, National Cancer Center, Goyang, Gyeonggi, 10408, Republic of Korea.
In-Hoo KimGraduate School of Cancer Science and Policy, National Cancer Center, Goyang, Gyeonggi, 10408, Republic of Korea.
Deog Su HwangDepartment of Biological Sciences, Seoul National University, Seoul, 08826, Republic of Korea.
Dae-Sik LimDepartment of Biological Sciences, Biomedical Research Center, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, Republic of Korea.
Ho LeeResearch Institute, National Cancer Center, Goyang, Gyeonggi, 10408, Republic of Korea. ho25lee@ncc.re.kr.
National Cancer Center · KRSeoul National University · KRKorea Advanced Institute of Science and Technology · KRNational Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Hippo pathway is involved in intestinal epithelial homeostasis with Wnt, BMP, Notch, and EGF signaling. We investigated the relationship between Hippo and other signaling pathways and the role of MOB kinase activator 1A/1B (MOB1A/B) in intestinal homeostasis. Mice with intestinal epithelial cell (IEC)-specific depletion of MOB1A/B showed hyperproliferation in IECs, defects in secretory lineage differentiation and loss of intestinal stem cells and eventually died at 10-12 days after tamoxifen treatment. In MOB1A/B-depleted IECs, expression of Wnt target genes were downregulated but Bmp2 and Tgfbr2 were transcriptionally activated with enhanced YAP activity. In in vivo and in vitro experiments with several signaling inhibitors, it has been shown that the BMP inhibitor LDN193189 or TGF-β inhibitor SB431542 had effects on partial restoration of the intestinal degenerative phenotype. Treatment with these inhibitors restored differentiation of secretory lineage cells in MOB1A/B-deficient mice, but not ISC pools in the crypt region. These studies reveal that IEC-specific depletion of MOB1A/B induced overexpression of Bmp2 and Tgfbr2 and inhibited Wnt activity, finally leading to loss of ISCs and functional epithelia in the mouse intestine. These results suggest that MOB1A/B has an essential function for intestinal epithelial homeostasis by regulating YAP, Wnt activity, and BMP/TGF-β signaling.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsBone Morphogenetic ProteinsCaco-2 CellsCell DifferentiationCell LineageCell Line, TumorCell ProliferationEpithelial CellsEpitheliumHomeostasisHumansIntestinal MucosaIntestinesIntracellular Signaling Peptides and ProteinsMiceAdaptor Proteins, Signal TransducingBone Morphogenetic ProteinsIntracellular Signaling Peptides and ProteinsMob1b protein, mouseMOB1 protein, mousePhosphoproteinsProtein KinasesTransforming Growth Factor beta

Identifiers

PMID30349003
PMCPMC6197243
OpenAlexW2897372492

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.