Evidence map›Paper›PMID 39207564›Full record

ArticleClinical and experimental medicine2024

TESC associated with poor prognosis enhances cancer stemness and migratory properties in liver cancer.

Peng Ye, Shahang Luo, Junyu Huang, Xihua Fu, Xiaoxia Chi, Jong-Ho Cha, Yumei Chen, Yanjun Mai, Kai-Wen Hsu, Xiuwen Yan and 1 more

Abstract read
In one paragraph

Article in Clinical and experimental medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Organoids and spheroids: advancedFrontiers in cell and developmental biology · 2024
    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

11 authors.

Peng Ye *Infection Medicine Research Institute of Panyu District, The Affiliated Panyu Central Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
Shahang Luo *Affiliated Cancer Hospital and Institute, Guangzhou Medical University, Guangzhou, Guangdong, China.
Junyu Huang *Graduate School of Guangzhou Medical University, Guangzhou Medical University, Guangzhou, Guangdong, China.
Xihua FuInfection Medicine Research Institute of Panyu District, The Affiliated Panyu Central Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
Xiaoxia ChiAffiliated Cancer Hospital and Institute, Guangzhou Medical University, Guangzhou, Guangdong, China.
Jong-Ho ChaDepartment of Biomedical Science, College of Medicine, and Program in Biomedical Sciences and Engineering, Inha University, Incheon, South Korea.
Yumei ChenInfection Medicine Research Institute of Panyu District, The Affiliated Panyu Central Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
Yanjun MaiInfection Medicine Research Institute of Panyu District, The Affiliated Panyu Central Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
Kai-Wen HsuInstitute of Translational Medicine and New Drug Development, China Medical University, Taichung, Taiwan. kwhsu@mail.cmu.edu.tw.
Xiuwen YanAffiliated Cancer Hospital and Institute, Guangzhou Medical University, Guangzhou, Guangdong, China. sure83@gzhmu.edu.cn.
Wen-Hao YangGraduate Institute of Cell Biology, China Medical University, Taichung, Taiwan. why0331@gmail.com.

Funding

Project of Educational Commission of Guangdong Province of China 2021KCXTD023the Internal Scientific Research Fund of Guangzhou Panyu Central Hospital PY-2023-025the National Natural Science Foundation of China 82172789the National Science and Technology Council, Taiwan NSTC 112-2320-B-039-024the Science and Technology Project of Guangzhou Health Commission 20241A011117the Science and Technology Project of Panyu District, Guangzhou 2023-Z04-021the YingTsai Young Scholar Award CMU108-YTY-04
6 · The paper itself

Abstract

Liver cancer stem cells (LCSCs) are responsible for recurrence, metastasis, and drug resistance in liver cancer. However, the genes responsible for inducing LCSCs have not been fully identified. Based on our previous study, we found that tescalcin (TESC), a calcium-binding EF hand protein that plays a crucial role in chromatin remodeling, transcriptional regulation, and epigenetic modifications, was up-regulated in LCSCs of spheroid cultures. By searching the Cancer Genome Atlas, International Cancer Genome Consortium, Human Protein Atlas, and Kaplan-Meier Plotter databases, we found that TESC expression was significantly elevated in liver cancer compared with that in normal liver tissue and was predictive of a decreased overall survival rate. Multivariate Cox analysis revealed TESC to be an independent prognostic factor for survival. High TESC expression was positively associated with cancer stem cell pathways, cancer stem cell surface markers, stemness transcription factors, epithelial-mesenchymal transition (EMT) factors, immune checkpoint proteins, and various cancer-related biological processes in liver cancer. Furthermore, TESC was implicated as promoting cancer stem cell properties through its influence on EMT. We demonstrated that TESC is a novel stemness-related gene that can serve as an independent prognostic factor for liver cancer.

Indexed as

Calcium-Binding ProteinsLiver NeoplasmsNeoplastic Stem CellsBiomarkers, TumorCell Line, TumorCell MovementEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedPrognosisBiomarkers, TumorCalcium-Binding ProteinsCancer stem cellsEMTHepatocellular carcinomaTESCTumor immunity

Identifiers

PMID39207564
PMCPMC11362204

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LicenceCC BY-NC-ND
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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.