Evidence map›Paper›PMID 28959047›Full record

ArticleScientific reports2017

Long non-coding RNA00544 serves as a potential novel predictive and prognostic marker for HR+ HER2- subtype breast cancer.

Lei Liu, Yayun Chi, Jiajian Chen, Jingyan Xue, Linlin Deng, Naisi Huang, Jianghua Shao, Jiong Wu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 86% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

8 authors at 4 institutions in 1 country.

Lei LiuDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Yayun ChiDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Jiajian ChenDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Jingyan XueDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Linlin DengDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Naisi HuangDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Jianghua ShaoDepartment of General Surgery, Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China. shao5022@163.com.
Jiong WuDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. wujiong1122@vip.sina.com.
Fudan University Shanghai Cancer Center · CNShanghai Medical College of Fudan University · CNNanchang University · CNSecond Affiliated Hospital of Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Luminal breast cancers (BC) account for majority of breast cancer. Due to its heterogeneity and the development of treatment resistance, luminal BC patients can vary substantially. Long noncoding RNAs (lncRNAs), as we known, is involved in breast cancer progression. Here, we aim to identify the lncRNAs which are involved in the particular type luminal BC progression. By Gene Chips analysis, we found a novel lncRNA00544, which was highly expressed in the metastatic axillary nodes compared with corresponding luminal BC tissues (fold change = 2.26, P = 0.043). This result was confirmed in luminal BC cell lines (p = 0.0113) and 49 paired breast cancer samples compared with in corresponding controls (p = 0.011). Furthermore, Kaplan-Meier survival curves of 373 breast cancer patients indicated that disease-free survival was significantly poor in breast cancer patients with high lncRNA00544 expression (p < 0.001). Univariate and multivariate Cox regression analyses showed that lncRNA00544 was a significant independent prognostic biomarker in luminal BC patients. Further analysis showed that the prognosis of high lncRNA00544 expression in breast cancer patients was actually related to HR + HER2- subtype. Together, our studies indicate that lncRNA00544 may represent a novel predictive and prognostic indicator in luminal BC patients.

Indexed as

AxillaBiomarkers, TumorBreast NeoplasmsCell Line, TumorDisease-Free SurvivalErb-b2 Receptor Tyrosine KinasesFemaleGene Expression ProfilingHumansKaplan-Meier EstimateLymph NodesMiddle AgedNeoplasm Recurrence, LocalOligonucleotide Array Sequence AnalysisPredictive Value of TestsPrognosisBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, ProgesteroneRNA, Long Noncoding

Identifiers

PMID28959047
PMCPMC5620366
OpenAlexW2759131985

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.