Evidence map›Paper›PMID 17260103›Full record

ArticleClinical & experimental metastasis2007

Isolation of a human gallbladder cancer cell clone with high invasive phenotype in vitro and metastatic potential in orthotopic model and inhibition of its invasiveness by heparanase antisense oligodeoxynucleotides.

Xin-Zhong Chang, Zhan-Min Wang, Jin-Ming Yu, Fu-Guo Tian, Wei Jin, Yi Zhang, Jie Yu, Lian-Fang Li, Xiao-Feng Liu, Zhi-Wei Li and 1 more

Abstract read
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Article in Clinical & experimental metastasis, 2007. 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
0.9field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

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  7. Mammalian heparanase: what is the message?Journal of cellular and molecular medicine
    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 at 7 institutions in 2 countries.

Xin-Zhong ChangCentral Laboratory, Cancer Hospital/Cancer Institute, Fudan University, Shanghai 200032, P. R. China.
Zhan-Min Wang
Jin-Ming Yu
Fu-Guo Tian
Wei Jin
Yi Zhang
Jie Yu
Lian-Fang Li
Xiao-Feng Liu
Zhi-Wei Li
Zhi-Min Shao
Fudan University Shanghai Cancer Center · CNQilu Hospital of Shandong University · CNBreast Cancer Research Foundation · USShandong First Medical University · CNShandong Tumor Hospital · CNShanxi Provincial Cancer Hospital · CNWeifang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mechanisms involved in gallbladder cancer metastasis still remain unclear to date. The poor understanding is due, in part, to the lack of ideal cell line and animal model for study. In the present study, 21 cell clones were isolated from the human gallbladder carcinoma cells GBC-SD and the cell clone GBC-SDH(i) with high invasive phenotype was fished out. The invasive phenotype and metastatic potential of GBC-SDH(i) were confirmed in a novel surgical orthotopic implantation model of gallbladder cancer in nude mice. Heparanase, an endoglycosidase that degrades heparan sulfate, is a critical mediator of tumor metastasis and angiogenesis. RT-PCR, real time RT-PCR and western blot showed that the expression levels of heparanase were significant difference between GBC-SDH(i) and its parent cells. After treated with antisense oligodeoxynucleotides, the heparanase mRNA and protein expression in GBC-SDH(i) cells were significantly decreased and its invasive potential in vitro was inhibited in a dose-dependent manner. The study provides a useful cell clone and a clinically relevant orthotopic tumor model for the metastatic study in human gallbladder cancer. The roles of heparanase in gallbladder cancer are also evaluated.

Indexed as

Neoplasm InvasivenessAnimalsBlotting, WesternCells, CulturedClone CellsDisease Models, AnimalElectrophoretic Mobility Shift AssayGallbladder NeoplasmsGlucuronidaseHeparanaseHumansMiceMice, NudeNeoplasm TransplantationOligonucleotides, AntisensePhenotypeGlucuronidaseHeparanaseOligonucleotides, Antisense

Identifiers

PMID17260103
OpenAlexW2030398827

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.