Evidence map›Paper›PMID 33257565›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

HSATII RNA is induced via a noncanonical ATM-regulated DNA damage response pathway and promotes tumor cell proliferation and movement.

Maciej T Nogalski, Thomas Shenk

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. 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
3.1field-weighted citation impact, top 7% 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, 27 citations in OpenAlex.

  1. Review
  2. Modeling the Copy Number of HSATII Repeats in Human Pericentromere.International journal of molecular sciences · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. Alpha Satellite DNA in Targeted Drug Therapy for Prostate Cancer.International journal of molecular sciences · 2023
    Article
  7. Review
  8. Chromatin conformational changes at human satellite II contribute to the senescence phenotype in the tumor microenvironment.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
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  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.

Maciej T NogalskiDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544-1014 nogalski@princeton.edu tshenk@princeton.edu.
Thomas ShenkDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544-1014 nogalski@princeton.edu tshenk@princeton.edu.
Princeton University · US

Funding

Human cytomegalovirus-induced alterations to cell-surface adhesion proteinsR01AI112951 · NIAID · PRINCETON UNIVERSITY · PI SHENK, THOMAS E · 2015 to 2019
$1.8M
An experimental system designed to identify human cytomegalovirus-induced alterations in tumor cells and test their dependence on continued viral gene expressionR21AI142520 · NIAID · PRINCETON UNIVERSITY · PI SHENK, THOMAS E · 2019 to 2020
$446k
Human cytomegalovirus-induced alterations to cell-surface adhesion proteinsR56AI112951 · NIAID · PRINCETON UNIVERSITY · PI SHENK, THOMAS E · 2014 to 2014
$399k
NIAID NIH HHS R01 AI112951NIAID NIH HHS R21 AI142520NIAID NIH HHS R56 AI112951
6 · The paper itself

Abstract

Pericentromeric human satellite II (HSATII) repeats are normally silent but can be actively transcribed in tumor cells, where increased HSATII copy number is associated with a poor prognosis in colon cancer, and in human cytomegalovirus (HCMV)-infected fibroblasts, where the RNA facilitates viral replication. Here, we report that HCMV infection or treatment of ARPE-19 diploid epithelial cells with DNA-damaging agents, etoposide or zeocin, induces HSATII RNA expression, and a kinase-independent function of ATM is required for the induction. Additionally, various breast cancer cell lines growing in adherent, two-dimensional cell culture express HSATII RNA at different levels, and levels are markedly increased when cells are infected with HCMV or treated with zeocin. High levels of HSATII RNA expression correlate with enhanced migration of breast cancer cells, and knockdown of HSATII RNA reduces cell migration and the rate of cell proliferation. Our investigation links high expression of HSATII RNA to the DNA damage response, centered on a noncanonical function of ATM, and demonstrates a role for the satellite RNA in tumor cell proliferation and movement.

Indexed as

Ataxia Telangiectasia Mutated ProteinsBleomycinBreast NeoplasmsCell Line, TumorCell MovementCell ProliferationCytomegalovirus InfectionsDisease ProgressionDNA DamageDNA RepairDNA, SatelliteEtoposideFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesGenetic FitnessAtaxia Telangiectasia Mutated ProteinsATM protein, humanBleomycinDNA, SatelliteEtoposideRNA, UntranslatedZeocinbreast cancer cellsDNA damage responseHSATIIhuman cytomegalovirushuman satellite II

Identifiers

PMID33257565
PMCPMC7749351
OpenAlexW3109989542

What Socratic 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 Socratic graph.