Evidence map›Paper›PMID 29312798›Full record

ArticleAmerican journal of cancer research2017

uc.38 induces breast cancer cell apoptosis via PBX1.

Lin-Xin Zhang, Lu Xu, Chen-Han Zhang, Yi-Han Lu, Tian-Hao Ji, Li-Jun Ling

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2017. 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
0.4field-weighted citation impact, top 39% 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, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. The regulation of PBXs and their emerging role in cancer.Journal of cellular and molecular medicine · 2022
    Review
  9. Article
  10. Article
  11. PBX1: a key character of the hallmarks of cancer.Journal of molecular medicine (Berlin, Germany) · 2021
    Review
  12. Article
  13. Article
  14. The Role of lncRNA in the Development of Tumors, including Breast Cancer.International journal of molecular sciences · 2021
    Review
  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

6 authors at 1 institution in 1 country.

Lin-Xin ZhangBreast Disease Division, The First Affiliated Hospital of Nanjing Medical UniversityNanjing, Jiangsu Province, China.
Lu XuBreast Disease Division, The First Affiliated Hospital of Nanjing Medical UniversityNanjing, Jiangsu Province, China.
Chen-Han ZhangBreast Disease Division, The First Affiliated Hospital of Nanjing Medical UniversityNanjing, Jiangsu Province, China.
Yi-Han LuBreast Disease Division, The First Affiliated Hospital of Nanjing Medical UniversityNanjing, Jiangsu Province, China.
Tian-Hao JiBreast Disease Division, The First Affiliated Hospital of Nanjing Medical UniversityNanjing, Jiangsu Province, China.
Li-Jun LingBreast Disease Division, The First Affiliated Hospital of Nanjing Medical UniversityNanjing, Jiangsu Province, China.
Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs) are transcripts longer than 200 bp with no protein-coding capacity. Transcribed ultraconserved regions (T-UCRs) are a type of lncRNA and are conserved among human, chick, dog, mouse and rat genomes. These sequences are involved in cancer biology and tumourigenesis. Nevertheless, the clinical significance and biological mechanism of T-UCRs in breast cancer remain largely unknown. The expression of uc.38, a T-UCR, was down-regulated in both breast cancer tissues and breast cancer cell lines. However, uc.38 was expressed at significantly lower levels in larger tumours and tumours of more advanced stages. Based on the results of in vitro and in vivo experiments, up-regulation of uc.38 expression inhibited cell proliferation and induced cell apoptosis. Thus, uc.38 suppressed breast cancer. Additional experiments revealed that uc.38 negatively regulated the expression of the pre-B-cell leukaemia homeobox 1 (PBX1) protein and subsequently affected the expression of Bcl-2 family members, ultimately inducing breast cancer cell apoptosis. Describing the uc.38/PBX1 axis has improved our understanding of the molecular mechanisms involved in breast cancer apoptosis and has suggested that this axis is a potential therapeutic target for breast cancer.

Indexed as

apoptosisbreast cancerLong non-coding RNApre-B-cell leukaemia homeobox 1proliferation

Identifiers

PMID29312798
PMCPMC5752685
OpenAlexW2970433000

What OpenQuestion 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 OpenQuestion graph.