Evidence map›Paper›PMID 31632466›Full record

ArticleTherapeutic advances in medical oncology2019

High-CLDN4 ESCC cells harbor stem-like properties and indicate for poor concurrent chemoradiation therapy response in esophageal squamous cell carcinoma.

Cheng-Han Lin, Hao-Yi Li, Yu-Peng Liu, Pei-Fung Kuo, Wen-Ching Wang, Forn-Chia Lin, Wei-Lun Chang, Bor-Shyang Sheu, Yi-Ching Wang, Wan-Chun Hung and 5 more

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

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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

15 authors at 4 institutions in 1 country.

Cheng-Han LinInstitute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan.
Hao-Yi LiInstitute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan.
Yu-Peng LiuInstitute of Clinical Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung.
Pei-Fung KuoInstitute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan.
Wen-Ching WangDepartment of Surgery, Chi Mei Medical Center, Tainan.
Forn-Chia LinDepartment of Radiation Oncology, National Cheng Kung University Hospital, Tainan.
Wei-Lun ChangInstitute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan.
Bor-Shyang SheuInstitute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan.
Yi-Ching WangDepartment of Pharmacology, College of Medicine, National Cheng Kung University, Tainan.ORCID https://orcid.org/0000-0002-7694-2067
Wan-Chun HungInstitute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan.
Hui-Chuan ChengInstitute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan.
Yun-Chin YaoClinical Medicine Research Center, National Cheng Kung University, Tainan.
Marcus J CalkinsInstitute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan.
Michael HsiaoGenomics Research Center, Academia Sinica, Taipei.ORCID https://orcid.org/0000-0001-8529-9213
Pei-Jung LuInstitute of Clinical Medicine, College of Medicine, National Cheng Kung University, No. 35, Siaodong Road, 704, Tainan.
National Cheng Kung University · TWNational Cheng Kung University Hospital · TWKaohsiung Medical University · TWChi Mei Medical Center · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEsophageal squamous cell carcinoma (ESCC) is the major type of esophageal cancer in Asia and demonstrates poor survival rates following a therapeutic regimen.

methodsCancer stem cells (CSCs) are responsible for tumor initiation, progression, and treatment failure in cancers. Therefore, identification and characterization of CSCs may help to improve clinical outcomes for ESCC patients. Tumor sphere formation assay are performed to isolate cancer stem-like ESCC cells. QRT-PCR, tumor initiation, metastasis, CCRT treatment are used to evaluate ESCC cells' stemness properties

resultsThe authors' data demonstrates that cancer stem-like ESCC cells harbored stemness characteristics including self-renewal, differentiation, and transdifferentiation, and possess tumor initiation, metastasis, and treatment inefficiency properties. For the identification of useful biomarkers of cancer stem-like ESCC cells, the authors further identified that CLDN4 was upregulated in cancer stem-like ESCC cells when compared with bulk cancer cells. High-CLDN4 cells harbored stemness and cisplatin/concurrent chemoradiation therapy (CCRT) resistance properties and a high level of CLDN4 was correlated with poor prognosis and poor CCRT response in ESCC patients. Importantly, thiamine tetrahydrofurfuryl disulfide (TTFD) decreased CLDN4 and attenuated stemness in ESCC cells, and TTFD combined with CCRT improved CCRT response

conclusionsCLDN4 was suggested as prognostic and a CCRT response indicator for ESCC patients. TTFD combined with CCRT has potential to improve ESCC patient's clinical outcomes in the future.

Indexed as

biomarkercancer stem-like cellsCCRTCLDN4concurrent chemoradiation therapyesophageal squamous cell carcinomathiamine tetrahydrofurfuryl disulfide (TTFD)

Identifiers

PMID31632466
PMCPMC6767752
OpenAlexW2975973552

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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.