Evidence map›Paper›PMID 32392629›Full record

ArticleMolecular oncology2020

Long non-coding NR2F1-AS1 is associated with tumor recurrence in estrogen receptor-positive breast cancers.

Anna Sanchez Calle, Tomofumi Yamamoto, Yumi Kawamura, Ai Hironaka-Mitsuhashi, Makiko Ono, Hitoshi Tsuda, Akihiko Shimomura, Kenji Tamura, Fumitaka Takeshita, Takahiro Ochiya and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

20 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  9. The genomic regulation of metastatic dormancy.Cancer metastasis reviews · 2023
    Review
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  20. Autophagy and Cancer Dormancy.Frontiers in oncology · 2021
    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

11 authors at 4 institutions in 1 country.

Anna Sanchez CalleDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Tomofumi YamamotoDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Yumi KawamuraDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Ai Hironaka-MitsuhashiDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Makiko OnoDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Hitoshi TsudaDepartment of Basic Pathology, National Defense Medical College, Saitama, Japan.
Akihiko ShimomuraDepartment of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Kenji TamuraDepartment of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Fumitaka TakeshitaDepartment of Functional analysis, National Cancer Center Research Institute, Tokyo, Japan.
Takahiro OchiyaDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Yusuke YamamotoDivision of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.ORCID 0000-0002-5262-8479
The Cancer Institute Hospital · JPTokyo Medical University · JPTokyo National Hospital · JPUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tenacity of late recurrence of estrogen receptor (ER)-positive breast cancer remains a major clinical issue to overcome. The administration of endocrine therapies within the first 5 years substantially minimizes the risk of relapse; however, some tumors reappear 10-20 years after the initial diagnosis. Accumulating evidence has strengthened the notion that long noncoding RNAs (lncRNAs) are associated with cancer in various respects. Because lncRNAs may display high tissue/cell specificity, we hypothesized this might provide new insights to tumor recurrence. By comparing transcriptome profiles of 24 clinical primary tumors obtained from patients who developed distant metastases and patients with no signs of recurrence, we identified lncRNA NR2F1-AS1 whose expression was associated with tumor recurrence. We revealed the relationship between NR2F1-AS1 and the hormone receptor expressions in ER-positive breast cancer cells. Gain of function of NR2F1-AS1 steered cancer cells into quiescence-like state by the upregulation of dormancy inducers and pluripotency markers, and activates representative events of the metastatic cascade. Our findings implicated NR2F1-AS1 in the dynamics of tumor recurrence in ER-positive breast cancers and introduce a new biomarker that holds a therapeutic potential, providing favorable prospects to be translated into the clinical field.

Indexed as

AnimalsBreast NeoplasmsCell CycleCell Line, TumorFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMiceNeoplasm MetastasisNeoplasm Recurrence, LocalReceptors, EstrogenReceptors, ProgesteroneRNA, Long NoncodingTranscription, GeneticReceptors, EstrogenReceptors, ProgesteroneRNA, Long NoncodingdormancyER-positive breast cancerlate recurrencelncRNAPR/ER transcriptional complex

Identifiers

PMID32392629
PMCPMC7463365
OpenAlexW3023360429

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.