Evidence map›Paper›PMID 31497347›Full record

ArticleAmerican journal of cancer research2019

Profiling the epigenetic interplay of lncRNA RUNXOR and oncogenic RUNX1 in breast cancer cells by gene in situ cis-activation.

Yuanyuan Nie, Lei Zhou, Hong Wang, Naifei Chen, Lin Jia, Cong Wang, Yichen Wang, Jingcheng Chen, Xue Wen, Chao Niu and 7 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Unveiling the Hidden Regulators: The Impact of lncRNAs on Zoonoses.International journal of molecular sciences · 2024
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Berberine Inhibits the Expression of SCT through miR-214-3p Stimulation in Breast Cancer Cells.Evidence-based complementary and alternative medicine : eCAM · 2020
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 1 institution in 1 country.

Yuanyuan NieStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Lei ZhouStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Hong WangStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Naifei ChenStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Lin JiaStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Cong WangStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Yichen WangStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Jingcheng ChenStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Xue WenStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Chao NiuStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Hui LiStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Rui GuoStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Songling ZhangStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Jiuwei CuiStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Andrew R HoffmanStanford University Medical School, VA Palo Alto Health Care System Palo Alto, CA 94304, USA.
Ji-Fan HuStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Wei LiStem Cell and Cancer Center, First Hospital, Jilin University Changchun 130061, Jilin, China.
Stanford University · US

Funding

BLRD VA I01 BX002905
6 · The paper itself

Abstract

RUNX1 is frequently mutated as chromosomal translocations in a variety of hematological malignancies. Recent studies show that RUNX1 is also mutated somatically in many solid tumors. We have recently identified a 260 kb un-spliced intragenic overlapping long noncoding RNA RUNXOR in the RUNX1 locus, yet its role as an epigenetic regulator in tumors remains to be characterized. To delineate this RUNXOR-RUNX1 regulatory interplay in breast cancer cells, we devised a novel "gene in situ cis-activation" approach to activate the endogenous RUNXOR gene. We found that the in situ activation of RUNXOR lncRNA upregulated RUNX1 in cis from the P1 promoter. The preferred activation of the P1 promoter caused a shift to the RUNX1c isoform expression. Using a chromatin conformation capture (3C) approach, we showed that RUNXOR lncRNA epigenetically activated the RUNX1 P1 promoter in cis by altering the local chromatin structure. The binding of RUNXOR lncRNA triggered DNA demethylation and induced active histone modification markers in the P1 CpG island. Changes in RUNX1 isoform composition correlated with a trend to cell cycle arrest at G0/G1, although cell proliferation rate, apoptosis, and migration ability were not significantly changed. Our results reveal an underlying epigenetic mechanism by which the lncRNA regulates in cis the RUNX1 promoter usage in breast cancer cells, thereby shedding light on potential genetic therapies in malignancies in which RUNX1 loss-of-function mutations frequently occur.

Indexed as

breast cancerEpigeneticslong noncoding RNARUNX1RUNXOR

Identifiers

PMID31497347
PMCPMC6726995
OpenAlexW2980489513

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.