Evidence map›Paper›PMID 24618814›Full record

ArticlePloS one2014

Detection of esophageal squamous cell carcinoma by cathepsin B activity in nude mice.

Wei Ma, Lie Ma, Hong Zhe, Cihang Bao, Nana Wang, Shaoqi Yang, Kai Wang, Fangli Cao, Yanna Cheng, Yufeng Cheng

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. A single nucleotide polymorphismInternational journal of clinical and experimental pathology · 2019
    Article
  4. Review
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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

10 authors.

Wei MaDepartment of Radiation Oncology, Qilu Hospital of Shandong University, Jinan, China; Department of Radiation Oncology, Cancer Hospital, General Hospital of Ningxia Medical University, Yinchuan, China.
Lie MaDepartment of Cardiology, Cardiovascular and Cerebrovascular Disease Hospital, General Hospital of Ningxia Medical University, Yinchuan, China.
Hong ZheDepartment of Radiation Oncology, Cancer Hospital, General Hospital of Ningxia Medical University, Yinchuan, China.
Cihang BaoDepartment of Radiation Oncology, Qilu Hospital of Shandong University, Jinan, China.
Nana WangDepartment of Radiation Oncology, Qilu Hospital of Shandong University, Jinan, China.
Shaoqi YangDigestive System Department, General Hospital of Ningxia Medical University, Yinchuan, China.
Kai WangDepartment of Oncology, Wendeng Center Hospital, Weihai, China.
Fangli CaoDepartment of Oncology, Liaocheng People's Hospital, Liaocheng, China.
Yanna ChengSchool of Pharmaceutical Sciences, Shandong University, Jinan, China.
Yufeng ChengDepartment of Radiation Oncology, Qilu Hospital of Shandong University, Jinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveDespite great progress in treatment, the prognosis for patients with esophageal squamous cell carcinoma (ESCC) remains poor, highlighting the importance of early detection. Although upper endoscopy can be used for the screening of esophagus, it has limited sensitivity for early stage disease. Thus, development of new diagnosis approach to improve diagnostic capabilities for early detection of ESCC is an important need. The aim of this study was to assess the feasibility of using cathepsin B (CB) as a novel imaging target for the detection of human ESCC by near-infrared optical imaging in nude mice.

methodsInitially, we examined specimens from normal human esophageal tissue, intraepithelial neoplasia lesions, tumor in situ, ESCC and two cell lines including one human ESCC cell line (Eca-109) and one normal human esophageal epithelial cell line (HET-1A) for CB expression by immunohistochemistry and western blot, respectively. Next, the ability of a novel CB activatable near-infrared fluorescence (NIRF) probe detecting CB activity presented in Eca-109 cells was confirmed by immunocytochemistry. We also performed in vivo imaging of tumor bearing mice injected with the CB probe and ex vivo imaging of resected tumor xenografts and visceral organs using a living imaging system. Finally, the sources of fluorescence signals in tumor tissue and CB expression in visceral organs were identified by histology.

resultsCB was absent in normal human esophageal mucosa, but it was overexpressed in ESCC and its precursor lesions. The novel probe for CB activity specifically detected ESCC xenografts in vivo and in vitro.

conclusionsCB was highly upregulated in human ESCC and its precursor lesions. The elevated CB expression in ESCC allowed in vivo and in vitro detection of ESCC xenografts in nude mice. Our results support the usefulness of CB activity as a potential imaging target for the detection of human ESCC.

Indexed as

AnimalsBiomarkers, TumorCarcinoma, Squamous CellCathepsin BCell Line, TumorDisease Models, AnimalEnzyme ActivationEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaGene ExpressionHeterograftsHumansMaleMiceMice, NudeMolecular ImagingBiomarkers, TumorCathepsin B

Identifiers

PMID24618814
PMCPMC3950293

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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.