Evidence map›Paper›PMID 35798764›Full record

ArticleScientific reports2022

Investigating the mechanisms of peritoneal metastasis in gastric adenocarcinoma using a novel ex vivo peritoneal explant model.

Deanna Ng, Aiman Ali, Kiera Lee, Denise Eymael, Kento Abe, Shelly Luu, Karineh Kazazian, Yi Qing Lu, Savtaj Brar, James Conner and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. 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
3.7field-weighted citation impact, top 6% 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, 18 citations in OpenAlex.

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  11. Exosomes secreted by ST3GAL5Molecular oncology · 2024
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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

12 authors at 6 institutions in 1 country.

Deanna NgInstitute of Medical Science, University of Toronto, Toronto, Canada.
Aiman AliFaculty of Dentistry, University of Toronto, Toronto, Canada.
Kiera LeeLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Canada.
Denise EymaelFaculty of Dentistry, University of Toronto, Toronto, Canada.
Kento AbeLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Canada.
Shelly LuuInstitute of Medical Science, University of Toronto, Toronto, Canada.
Karineh KazazianInstitute of Medical Science, University of Toronto, Toronto, Canada.
Yi Qing LuLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Canada.
Savtaj BrarDepartment of Surgical Oncology and Division of General Surgery, Princess Margaret Cancer Centre, University Health Network/Mount Sinai Hospital, 600 University Avenue #1225, Toronto, ON, M5G 1X5, Canada.
James ConnerDepartment of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Canada.
Marco Magalhaes *Institute of Medical Science, University of Toronto, Toronto, Canada.
Carol J Swallow *Institute of Medical Science, University of Toronto, Toronto, Canada. Carol.Swallow@sinaihealth.ca.
Lunenfeld-Tanenbaum Research Institute · CAUniversity of Toronto · CASinai Health System · CAMount Sinai Hospital · CAPrincess Margaret Cancer Centre · CAUniversity Health Network · CA

Funding

CIHR PJ7-169674CIHR PJT-17512
6 · The paper itself

Abstract

Gastric adenocarcinoma, commonly known as stomach cancer, has a predilection for metastasis to the peritoneum, which portends limited survival. The peritoneal metastatic cascade remains poorly understood, and existing models fail to recapitulate key elements of the interaction between cancer cells and the peritoneal layer. To explore the underlying cellular and molecular mechanisms of peritoneal metastasis, we developed an ex vivo human peritoneal explant model. Fresh peritoneal tissue samples were suspended, mesothelial layer down but without direct contact, above a monolayer of red-fluorescent dye stained AGS human gastric adenocarcinoma cells for 24 h, then washed thoroughly. Implantation of AGS cells within the explanted peritoneum and invasion beyond the mesothelial layer were examined serially using real-time confocal fluorescence microscopy. Histoarchitecture of the explanted peritoneum was preserved over 5 days ex vivo. Both implantation and invasion were suppressed by restoration of functional E-cadherin through stable transfection of AGS cells, demonstrating sensitivity of the model to molecular manipulation. Thus, our ex vivo human peritoneal explant model permits meaningful investigation of the pathways and mechanism that contribute to peritoneal metastasis. The model will facilitate screening of new therapies that target peritoneal dissemination of gastric, ovarian and colorectal cancer.

Indexed as

AdenocarcinomaPeritoneal NeoplasmsStomach NeoplasmsCell Line, TumorHumansPeritoneum

Identifiers

PMID35798764
PMCPMC9262973
OpenAlexW4284886537

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.