Evidence map›Paper›PMID 28327601›Full record

ArticleScientific reports2017

BCIP: a gene-centered platform for identifying potential regulatory genes in breast cancer.

Jiaqi Wu, Shuofeng Hu, Yaowen Chen, Zongcheng Li, Jian Zhang, Hanyu Yuan, Qiang Shi, Ningsheng Shao, Xiaomin Ying

Erratum issuedOpen 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. An erratum has been issued. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.1field-weighted citation impact, top 22% 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.

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  14. Diagnostic and prognostic value of thymidylate synthase expression in breast cancer.Clinical and experimental pharmacology & physiology · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Jiaqi WuBeijing Institute of Basic Medical Sciences, Beijing 100850, China.
Shuofeng HuBeijing Institute of Basic Medical Sciences, Beijing 100850, China.
Yaowen ChenBeijing Institute of Basic Medical Sciences, Beijing 100850, China.
Zongcheng LiBeijing Institute of Basic Medical Sciences, Beijing 100850, China.
Jian ZhangBeijing Institute of Basic Medical Sciences, Beijing 100850, China.
Hanyu YuanBeijing Institute of Basic Medical Sciences, Beijing 100850, China.
Qiang ShiBeijing Institute of Basic Medical Sciences, Beijing 100850, China.
Ningsheng ShaoBeijing Institute of Basic Medical Sciences, Beijing 100850, China.
Xiaomin YingBeijing Institute of Basic Medical Sciences, Beijing 100850, China.
Beijing Institute of Education · CNInstitute of Basic Medical Sciences of the Chinese Academy of Medical Sciences

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is a disease with high heterogeneity. Many issues on tumorigenesis and progression are still elusive. It is critical to identify genes that play important roles in the progression of tumors, especially for tumors with poor prognosis such as basal-like breast cancer and tumors in very young women. To facilitate the identification of potential regulatory or driver genes, we present the Breast Cancer Integrative Platform (BCIP, http://omics.bmi.ac.cn/bcancer/). BCIP maintains multi-omics data selected with strict quality control and processed with uniform normalization methods, including gene expression profiles from 9,005 tumor and 376 normal tissue samples, copy number variation information from 3,035 tumor samples, microRNA-target interactions, co-expressed genes, KEGG pathways, and mammary tissue-specific gene functional networks. This platform provides a user-friendly interface integrating comprehensive and flexible analysis tools on differential gene expression, copy number variation, and survival analysis. The prominent characteristic of BCIP is that users can perform analysis by customizing subgroups with single or combined clinical features, including subtypes, histological grades, pathologic stages, metastasis status, lymph node status, ER/PR/HER2 status, TP53 mutation status, menopause status, age, tumor size, therapy responses, and prognosis. BCIP will help to identify regulatory or driver genes and candidate biomarkers for further research in breast cancer.

Indexed as

Gene Expression Regulation, NeoplasticGene Regulatory NetworksSoftwareBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesFemaleHumansNeoplasm MetastasisTumor Suppressor Protein p53ERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID28327601
PMCPMC5361122
OpenAlexW2598588612

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.