Evidence map›Paper›PMID 36992525›Full record

ArticleCancer medicine2023

Inhibition of lncRNA PCAT19 promotes breast cancer proliferation.

Jianyuan Feng, Jiarui Zhang, Yanling Li, Weilun Cheng, Yansong Liu, Ziang Chen, Yunqiang Duan, Tianshui Yu, Anbang Hu, Ting Wang and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. PCAT19: the role in cancer pathogenesis and beyond.Frontiers in cell and developmental biology · 2024
    Review
  8. Article
  9. 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

15 authors at 1 institution in 1 country.

Jianyuan FengDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Jiarui ZhangDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Yanling LiDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Weilun ChengDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Yansong LiuDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Ziang ChenDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Yunqiang DuanDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Tianshui YuDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Anbang HuDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Ting WangDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Hanyu ZhangDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Mingcui LiDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Zhiyuan RongDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Fei MaDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Baoliang GuoDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.ORCID 0000-0002-4022-6739
Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer (BC) is the most common malignancy affecting women. It is vital to explore sensitive biological markers to diagnose and treat BC patients. Recent studies have proved that long noncoding RNAs (lncRNAs) were involved in breast tumor progression. Nonetheless, whether lncRNA prostate cancer-associated transcript 19 (PCAT19) impacts BC development remains unknown.

methodsWe performed various bioinformatic analyses, including machine learning models to identify critical regulatory lncRNAs affecting prognosis in BC. The in situ hybridization (ISH) assay was carried out to confirm the expression levels of lncRNA PCAT19 in tissue specimens. MTT assay, wound healing assay, and transwell assay were performed to investigate PCAT19's impact on proliferation, migration, and invasion of BC cells. Mouse xenografts were used to examine the proliferation-inhibiting function of PCAT19 in vivo.

resultsAmong the prognosis-associated lncRNAs, PCAT19 predicted a favorable prognosis in BC. Patients with high expression levels of PCAT19 had a lower clinical stage and less lymph node metastasis. The PCAT19-related genes were enriched in signaling pathways involved in tumor development, indicating PCAT19 was an essential regulator of BC. Using the ISH assay, we confirmed the expression level of lncRNA PCAT19 in human BC tissues was lower than normal breast tissues. Moreover, the knockdown of PCAT19 further confirmed its inhibiting ability in BC cell proliferation. Correspondingly, overexpressing PCAT19 reduced tumor size in mouse xenografts.

conclusionsOur study demonstrated that lncRNA PCAT19 suppressed the development of BC. PCAT19 might be a promising prognostic biomarker, which provides new insights into risk stratification for BC patients.

Indexed as

Breast NeoplasmsMicroRNAsRNA, Long NoncodingAnimalsCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMaleMicePrognosisMicroRNAsRNA, Long Noncodingbioinformaticsbreast cancerlong noncoding RNAtumor biology

Identifiers

PMID36992525
PMCPMC10242319
OpenAlexW4361276850

What OpenQuestion holds

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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.