Evidence map›Paper›PMID 32840881›Full record

ReviewJournal of cellular physiology2021

Chromatin regulators in retinoblastoma: Biological roles and therapeutic applications.

Chunsik Lee, Jong Kyong Kim

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of cellular physiology, 2021. 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
1.2field-weighted citation impact, top 22% 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, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Retinoblastoma: Review and new insights.Frontiers in oncology · 2022
    Review
  12. Article
  13. Article
  14. Netrin-1 promotes retinoblastoma-associated angiogenesis.Annals of translational medicine · 2021
    Article
  15. Article
  16. Review
  17. 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

2 authors at 1 institution in 1 country.

Chunsik LeeState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China.
Jong Kyong KimState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China.ORCID 0000-0001-7930-723X
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Retinoblastoma (RB) is a pediatric ocular tumor mostly occurring due to the biallelic loss of RB1 gene in the developing retina. Early studies of genomic aberrations in RB have provided a valuable insight into how RB can progress following the tumor-initiating RB1 mutations and have established a notion that inactivation of RB1 gene is critical to initiate RB but this causative genetic lesion alone is not sufficient for malignant progression. With the advent of high-throughput sequencing technologies, we now have access to the comprehensive genomic and epigenetic landscape of RB and have come to appreciate that RB tumorigenesis requires both genetic and epigenetic alterations that might be directly or indirectly driven by RB1 loss. This integrative perspective on RB tumorigenesis has inspired research efforts to better understand the types and functions of epigenetic mechanisms contributing to RB development, leading to the identification of multiple epigenetic regulators misregulated in RB in recent years. A complete understanding of the intricate network of genetic and epigenetic factors in modulation of gene expression during RB tumorigenesis remains a major challenge but would be crucial to translate these findings into therapeutic interventions. In this review, we will provide an overview of chromatin regulators identified to be misregulated in human RB among the numerous epigenetic factors implicated in RB development. For a subset of these chromatin regulators, recent findings on their functions in RB development and potential therapeutic applications are discussed.

Indexed as

Chromatin Assembly and DisassemblyEpigenesis, GeneticAnimalsCCAAT-Enhancer-Binding ProteinsDNA HelicasesDNA MethylationE2F Transcription FactorsEnhancer of Zeste Homolog 2 ProteinGene Expression Regulation, NeoplasticHistone Deacetylase InhibitorsHMGA2 ProteinHumansMolecular Targeted TherapyPolycomb Repressive Complex 1Retinal NeoplasmsRetinoblastomaBMI1 protein, humanCCAAT-Enhancer-Binding ProteinsDNA HelicasesE2F Transcription FactorsEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanHELLS protein, humanHistone Deacetylase InhibitorsHMGA2 ProteinHMGA2 protein, humanPolycomb Repressive Complex 1Transcription FactorsUbiquitin-Protein LigasesUHRF1 protein, humanchromatinepigenetic regulatorocular tumorretinoblastomaretinogenesistargeted therapy

Identifiers

PMID32840881
PMCPMC7891620
OpenAlexW3080427610

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.