Evidence map›Paper›PMID 34849865›Full record

ArticleHuman molecular genetics2022

Disease-associated c-MYC downregulation in human disorders of transcriptional regulation.

Maria M Pallotta, Maddalena Di Nardo, Patrizia Sarogni, Ian D Krantz, Antonio Musio

Open access · greenAbstract read
In one paragraph

Article in Human molecular genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Cornelia de Lange syndrome and cancer: An open question.American journal of medical genetics. Part A · 2023
    Article
  7. The multifaceted roles of cohesin in cancer.Journal of experimental & clinical cancer research : CR · 2022
    Review
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

5 authors at 3 institutions in 2 countries.

Maria M PallottaInstitute for Genetic and Biomedical Research (IRGB), National Research Council (CNR), 56124 Pisa, Italy.
Maddalena Di NardoInstitute for Genetic and Biomedical Research (IRGB), National Research Council (CNR), 56124 Pisa, Italy.
Patrizia SarogniInstitute for Genetic and Biomedical Research (IRGB), National Research Council (CNR), 56124 Pisa, Italy.
Ian D KrantzRoberts Individualized Medical Genetics Center, Division of Human Genetics, The Department of Pediatrics, The Children's Hospital of Philadelphia, and the Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
Antonio MusioInstitute for Genetic and Biomedical Research (IRGB), National Research Council (CNR), 56124 Pisa, Italy.
Institute of Genetic and Biomedical Research · ITChildren's Hospital of Philadelphia · USNational Research Council · IT

Funding

Genomic Diagnostics in Cornelia de Lange Syndrome, Related Diagnosis and Structural Birth DefectsR03HD099530 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI KRANTZ, IAN D. · 2019 to 2020
$352k
NICHD NIH HHS R03 HD099530
6 · The paper itself

Abstract

Cornelia de Lange syndrome (CdLS) is a rare multiorgan developmental disorder caused by pathogenic variants in cohesin genes. It is a genetically and clinically heterogeneous dominant (both autosomal and X-linked) rare disease. Increasing experimental evidence indicates that CdLS is caused by a combination of factors, such as gene expression dysregulation, accumulation of cellular damage and cellular aging, which collectively contribute to the CdLS phenotype. The CdLS phenotype overlaps with a number of related diagnoses such as KBG syndrome and Rubinstein-Taybi syndrome both caused by variants in chromatin-associated factors other than cohesin. The molecular basis underlying these overlapping phenotypes is not clearly defined. Here, we found that cells from individuals with CdLS and CdLS-related diagnoses are characterized by global transcription disturbance and share common dysregulated pathways. Intriguingly, c-MYC (subsequently referred to as MYC) is downregulated in all cell lines and represents a convergent hub lying at the center of dysregulated pathways. Subsequent treatment with estradiol restores MYC expression by modulating cohesin occupancy at its promoter region. In addition, MYC activation leads to modification in expression in hundreds of genes, which in turn reduce the oxidative stress level and genome instability. Together, these results show that MYC plays a pivotal role in the etiopathogenesis of CdLS and CdLS-related diagnoses and represents a potential therapeutic target for these conditions.

Indexed as

Abnormalities, MultipleBone Diseases, DevelopmentalDe Lange SyndromeIntellectual DisabilityTooth AbnormalitiesCell Cycle ProteinsDown-RegulationFaciesHumansMutationPhenotypeProto-Oncogene Proteins c-mycCell Cycle ProteinsMYC protein, humanProto-Oncogene Proteins c-myc

Identifiers

PMID34849865
PMCPMC9122636
OpenAlexW3215681480

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.