Evidence map›Paper›PMID 26847082›Full record

ArticleBMC cancer2016

Establishment and characterization of a metastasis model of human gastric cancer in nude mice.

Kesheng Li, Huifen Du, Xiaowen Lian, Dandan Chai, Xinwen Li, Rong Yang, Chunya Wang

Abstract read
In one paragraph

Article in BMC cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

7 authors.

Kesheng LiDepartment of Medicine Biotechnology, Medicine and Science Research Institute of Gansu province, Lanzhou, China. likesheng63@hotmail.com.
Huifen DuDepartment of Medicine Biotechnology, Medicine and Science Research Institute of Gansu province, Lanzhou, China.
Xiaowen LianDepartment of Medicine Biotechnology, Medicine and Science Research Institute of Gansu province, Lanzhou, China.
Dandan ChaiDepartment of Medicine Biotechnology, Medicine and Science Research Institute of Gansu province, Lanzhou, China.
Xinwen LiDepartment of Surgery, Tumor Hospital of Gansu province, Lanzhou, China.
Rong YangDepartment of pathology, Tumor Hospital of Gansu province, Lanzhou, China.
Chunya WangDepartment of Medicine Biotechnology, Medicine and Science Research Institute of Gansu province, Lanzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA mouse model of metastasis of human gastric cancer is one of the most important tools for studying the biological mechanisms underlying human gastric cancer metastasis. In this paper, we established a mouse model of metastatic human gastric cancer in nude mice that has a higher rate of tumor formation and metastasis than existing models.

methodsTo generate the mouse model of metastatic human gastric cancer, fresh tumor tissues from patients that have undergone surgery for gastric cancer were subcutaneously implanted in the right and left groins of nude mice. When the implanted tissue grew to 1 cubic centimeter, the mice were killed, and the tumor tissues were examined and resected. The tumor tissues were implanted into nude mice and subjected to pathological examination, immunohistochemical staining, and real-time PCR for cytokeratin 8/18 (CK8/18), E-cadherin, vascular cell adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1). The mice were also analyzed for metastasis in their peritoneum, abdominal cavity, and internal organs by histopathological examination. Tissues collected from these organs were examined for pathology.

resultsAfter ten generations of implantation, all mice developed tumor growth at the implanted position, 94% of the mice developed metastasis to the retroperitoneum and viscera. The implanted and metastatic tumor maintained the same histological features across all generations, and metastasis was observed in the esophagus, stomach, spleen, liver, kidney, adrenal, intestine, and pancreas. These metastatic tumors revealed no detectable expression of CK8/18, E-cadherin, VCAM-1, and ICAM-1.

conclusionsThis model will serve as valuable tool for understanding the metastatic process of human gastric cancer.

Indexed as

AnimalsCadherinsCell Line, TumorDisease Models, AnimalGene Expression Regulation, NeoplasticHumansIntercellular Adhesion Molecule-1Keratin-8MiceNeoplasm MetastasisStomach NeoplasmsTissue DistributionVascular Cell Adhesion Molecule-1CadherinsIntercellular Adhesion Molecule-1Keratin-8Vascular Cell Adhesion Molecule-1

Identifiers

PMID26847082
PMCPMC4741000

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LicenceCC BY
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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.