Evidence map›Paper›PMID 29993199›Full record

ArticleJournal of cellular and molecular medicine2018

The oncogenic potentials and diagnostic significance of long non-coding RNA LINC00310 in breast cancer.

Juan Li, Wanxin Peng, Lutao Du, Qifeng Yang, Chuanxin Wang, Yin-Yuan Mo

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Arterial dissections: Common features and new perspectives.Frontiers in cardiovascular medicine · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Observational
  13. Cancer-associated methylated lncRNAs in patients with bladder cancer.American journal of translational research · 2019
    Article
  14. 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 4 institutions in 2 countries.

Juan LiDepartment of Clinical Laboratory, The Second Hospital of Shandong University, Jinan, Shandong Province, China.
Wanxin PengCancer Institute, University of Mississippi Medical Center, Jackson, MS, USA.
Lutao DuDepartment of Clinical Laboratory, The Second Hospital of Shandong University, Jinan, Shandong Province, China.
Qifeng YangDepartment of Breast Surgery, Qilu Hospital, Shandong University, Jinan, Shandong Province, China.
Chuanxin WangDepartment of Clinical Laboratory, The Second Hospital of Shandong University, Jinan, Shandong Province, China.ORCID 0000-0002-3796-6293
Yin-Yuan MoCancer Institute, University of Mississippi Medical Center, Jackson, MS, USA.
Jackson Memorial Hospital · USSecond Hospital of Shandong University · CNJiangsu University · CNQilu Hospital of Shandong University · CN

Funding

The Akt-associated microRNAs in cancer cellsR01CA154989 · NCI · UNIVERSITY OF MISSISSIPPI MED CTR · PI MO, YIN-YUAN · 2011 to 2015
$1.5M
NCI NIH HHS R01 CA154989
6 · The paper itself

Abstract

Recent studies have revealed that long non-coding RNAs (lncRNAs) are involved in different physiological processes and human diseases. However, to date, the function and overall clinical significance of the vast majority of lncRNAs in breast cancer remain largely unexplored. Here, we focused on LINC00310 by interrogating the breast invasive carcinoma data set of the Cancer Genome Atlas (TCGA). The results showed that LINC00310 was increased as breast cancer progressed, and the deregulation of LINC00310 was significantly associated with patients' survival. Experiments with knockout (KO) approach by CRISPR/Cas9 system and the subsequent rescue experiments revealed that LINC00310 promoted cell proliferation by regulating c-Myc expression in vitro. Nude mouse xenograft assay demonstrated that LINC00310 KO significantly suppressed tumour growth in vivo. Furthermore, we found that serum LINC00310 expression was significantly up-regulated in patients with breast cancer, and receiver operating characteristic (ROC) curve analysis indicated that LINC00310 had a powerful capability of distinguishing patients with breast cancer from healthy individuals (the area under curve 0.828). Taken together, these results provide a more intuitive approach to explore the clinical relevance and functional roles of lncRNAs. As a result, lncRNAs, such as LINC00310, may be used in clinical applications as circulating markers for breast cancer.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBreast NeoplasmsCarcinogenesisCase-Control StudiesCell Line, TumorCell ProliferationCRISPR-Cas SystemsFemaleHumansMiceMice, NudeOligoribonucleotidesPrognosisProto-Oncogene Proteins c-mycRNA, Long NoncodingMYC protein, humanOligoribonucleotidesProto-Oncogene Proteins c-mycRNA, Long Noncodingbreast cancerdiagnosisLINC00310oncogenic roleprognosis

Identifiers

PMID29993199
PMCPMC6111859
OpenAlexW2859718959

What OpenQuestion holds

Textmetadata
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.