Evidence map›Paper›PMID 31850052›Full record

ArticleFrontiers in genetics2019

Comprehensive Analysis of Therapy-Related Messenger RNAs and Long Noncoding RNAs as Novel Biomarkers for Advanced Colorectal Cancer.

Jibin Li, Siping Ma, Tao Lin, Yanxi Li, Shihua Yang, Wanchuan Zhang, Rui Zhang, Yongpeng Wang

Abstract read
In one paragraph

Article in Frontiers in genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. A concise review on the role of MIR100HG in human disorders.Journal of cellular and molecular medicine · 2023
    Review
  3. Review
  4. Article
  5. Article
  6. 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

8 authors.

Jibin LiDepartment of Colorectal Surgery, Liaoning Cancer Hospital, Cancer Hospital of China Medical University, Shenyang, China.
Siping MaDepartment of Colorectal Surgery, Liaoning Cancer Hospital, Cancer Hospital of China Medical University, Shenyang, China.
Tao LinDepartment of Colorectal Surgery, Liaoning Cancer Hospital, Cancer Hospital of China Medical University, Shenyang, China.
Yanxi LiDepartment of Colorectal Surgery, Liaoning Cancer Hospital, Cancer Hospital of China Medical University, Shenyang, China.
Shihua YangChina Medical University, Shenyang, China.
Wanchuan ZhangChina Medical University, Shenyang, China.
Rui ZhangDepartment of Colorectal Surgery, Liaoning Cancer Hospital, Cancer Hospital of China Medical University, Shenyang, China.
Yongpeng WangDepartment of Colorectal Surgery, Liaoning Cancer Hospital, Cancer Hospital of China Medical University, Shenyang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is one of the most common types of human cancers. However, the mechanisms underlying CRC progression remained elusive. This study identified differently expressed messenger RNAs (mRNAs), long noncoding RNAs (lncRNAs), and small nucleolar RNAs (snoRNAs) between pre-therapeutic biopsies and post-therapeutic resections of locally advanced CRC by analyzing a public dataset, GSE94104. We identified 427 dysregulated mRNAs, 4 dysregulated lncRNAs, and 19 dysregulated snoRNAs between pre- and post-therapeutic locally advanced CRC samples. By constructing a protein-protein interaction network and co-expressing networks, we identified 10 key mRNAs, 4 key lncRNAs, and 7 key snoRNAs. Bioinformatics analysis showed therapy-related mRNAs were associated with nucleosome assembly, chromatin silencing at recombinant DNA, negative regulation of gene expression, and DNA replication. Therapy-related lncRNAs were associated with cell adhesion, extracellular matrix organization, angiogenesis, and sister chromatid cohesion. In addition, therapy-related snoRNAs were associated with DNA replication, nucleosome assembly, and telomere organization. We thought this study provided useful information for identifying novel biomarkers for CRC.

Indexed as

co-expression analysiscolorectal cancerexpression profilinglong noncoding RNAprognostic markersprotein–protein interaction analysissnoRNAs

Identifiers

PMID31850052
PMCPMC6900565

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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.