Evidence map›Paper›PMID 32311840›Full record

ArticleCancer medicine2020

Identification of cancer stem cell characteristics in liver hepatocellular carcinoma by WGCNA analysis of transcriptome stemness index.

Kun-Hao Bai, Si-Yuan He, Ling-Ling Shu, Wei-Da Wang, Shi-Yong Lin, Qian-Yi Zhang, Liang Li, Lei Cheng, Yu-Jun Dai

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

71 citing papers in PubMed, 114 citations in OpenAlex.

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  15. Unveiling the oncogenic role of LZTS1 in colorectal cancer.Journal of cellular and molecular medicine · 2024
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11 more citing papers are in PubMed but not listed here.

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

9 authors at 5 institutions in 2 countries.

Kun-Hao BaiDepartment of Endoscopy, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Si-Yuan HeThe University of Texas MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, Houston, TX, USA.
Ling-Ling ShuState Key Laboratory of Oncology in South China, Guangzhou, China.
Wei-Da WangState Key Laboratory of Oncology in South China, Guangzhou, China.
Shi-Yong LinDepartment of Endoscopy, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Qian-Yi ZhangState Key Laboratory of Oncology in South China, Guangzhou, China.
Liang LiState Key Laboratory of Oncology in South China, Guangzhou, China.
Lei ChengCollaborative Innovation Center for Cancer Medicine, Cancer Institute, Fudan University Shanghai Cancer Center, Shanghai, China.
Yu-Jun DaiState Key Laboratory of Oncology in South China, Guangzhou, China.
Sun Yat-sen University Cancer Center · CNState Key Laboratory of Oncology in South ChinaFudan University Shanghai Cancer Center · CNSun Yat-sen University · CNThe University of Texas Health Science Center at Houston · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer stem cells (CSCs) are characterized by self-renewal and -differential potential as compared to common cancer cells and play an important role in the development and therapeutic resistance of liver hepatocellular carcinoma (LIHC). However, the specific pathogenesis of LIHC stem cells is still unclear, and the genes involved in the stemness of LIHC stem cells are currently unknown. In this study, we investigated novel biomarkers associated with LIHC and explored the expression characteristics of stem cell-related genes in LIHC. We found that mRNA expression-based stemness index (mRNAsi) was significantly overexpressed in liver cancer tissues. Further, mRNAsi expression in LIHC increased with the tumor pathological grade, with grade 4 tumors harboring the greatest stem cell features. Upon establishing mRNAsi scores based on mRNA expression of every gene, we found an association with poor overall survival in LIHC. Moreover, modules of interest were determined based on weighted gene co-expression network analysis (WGCNA) inclusion criteria, and three significant modules (red, green, and brown) and 21 key genes (DCN, ECM1, HAND2, PTGIS, SFRP1, SRPX, COLEC10, GRP182, ADAMTS7, CD200, CDH11, COL8A1, FAP, LZTS1, MAP1B, NAV1, NOTCH3, OLFML2A, PRR16, TMEM119, and VCAN) were identified. Functional analysis of these 21 genes demonstrated their enrichment in pathways involved in angiogenesis, negative regulation of DNA-binding transcription factor activity, apoptosis, and autophagy. Causal relationship with proteins indicated that the Wnt, Notch, and Hypoxia pathways are closely related to LIHC tumorigenesis. To our knowledge, this is the first report of a novel CSC biomarker, mRNAsi, to predict the prognosis of LIHC. Further, we identified 21 key genes through mRNA expression network analysis, which could be potential therapeutic targets to inhibit the stemness of cancer cells in LIHC.

Indexed as

Gene Expression Regulation, NeoplasticTranscriptomeBiomarkers, TumorCarcinoma, HepatocellularGene Expression ProfilingGene Regulatory NetworksHumansLiver NeoplasmsNeoplastic Stem CellsBiomarkers, Tumorbiomarkercancer stem cells (CSCs)co-expression networkliver hepatocellular carcinoma (LIHC)mRNAsi indexWGCNA analysis

Identifiers

PMID32311840
PMCPMC7300398
OpenAlexW3017331726

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.