Evidence map›Paper›PMID 29765542›Full record

ArticleOncotarget2018

SMAR1 inhibits Wnt/β-catenin signaling and prevents colorectal cancer progression.

Nandaraj Taye, Aftab Alam, Suvankar Ghorai, Deya Ghosh Chatterji, Apoorva Parulekar, Devraj Mogare, Snahlata Singh, Pallabi Sengupta, Subhrangsu Chatterjee, Manoj Kumar Bhat and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Histone Modification of Colorectal Cancer by Natural Products.Pharmaceuticals (Basel, Switzerland) · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. The Role ofJournal of immunology research · 2021
    Article
  12. Review
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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

14 authors at 6 institutions in 1 country.

Nandaraj TayeNational Centre for Cell Science, Pune 411 007, India.
Aftab AlamNational Centre for Cell Science, Pune 411 007, India.
Suvankar GhoraiSRM University, Tamil Nadu, Kattankulathur 603 203, India.
Deya Ghosh ChatterjiNKP Salve Institute of Medical Sciences, Nagpur, 440 019, India.
Apoorva ParulekarNational Centre for Cell Science, Pune 411 007, India.
Devraj MogareNational Centre for Cell Science, Pune 411 007, India.
Snahlata SinghNational Centre for Cell Science, Pune 411 007, India.
Pallabi SenguptaDepartment of Biophysics, Bose Institute, Kolkata 700 054, India.
Subhrangsu ChatterjeeDepartment of Biophysics, Bose Institute, Kolkata 700 054, India.
Manoj Kumar BhatNational Centre for Cell Science, Pune 411 007, India.
Manas Kumar SantraNational Centre for Cell Science, Pune 411 007, India.
Prabhakar Budha SalunkheAmrita Therapeutics Limited, Ahmedabad 380 054, India.
Susan Kling FinstonAmrita Therapeutics Limited, Ahmedabad 380 054, India.
Samit ChattopadhyayNational Centre for Cell Science, Pune 411 007, India.
National Centre for Cell Science · INAmrita Therapeutics (India) · INBose Institute · INIndian Institute of Chemical Biology · INNKP Salve Institute of Medical Sciences and Lata Mangeshkar Hospital · INSRM University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reduced expression of Scaffold/Matrix Attachment Region Binding Protein 1 (SMAR1) is associated with various cancers resulting in poor prognosis of the diseases. However, the precise underlying mechanism elucidating the loss of SMAR1 requires ongoing study. Here, we show that SMAR1 is highly downregulated during aberrant Wnt3a signaling due to proteasomal degradation and predicted poor prognosis of colorectal cancer. However, substitution mutation (Arginine and Lysine to Alanine) in the D-box elements of SMAR1 viz. "RCHL" and "RQRL" completely abrogated its proteasomal degradation despite Wnt3a activity. SMAR1 inhibited Wnt/β-catenin signaling by recruiting Histone deacetylase-5 to β-catenin promoter resulting in reduced cell migration and invasion. Consequently, reduced tumor sizes in

Indexed as

conditioned mediumpeptideSMAR1Wnt3aβ-catenin

Identifiers

PMID29765542
PMCPMC5940383
OpenAlexW2803052455

What OpenQuestion holds

Textmetadata
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.