Evidence map›Paper›PMID 26484588›Full record

ArticleJournal of visualized experiments : JoVE2015

The In Ovo Chick Chorioallantoic Membrane (CAM) Assay as an Efficient Xenograft Model of Hepatocellular Carcinoma.

Michael Li, Ravi R Pathak, Esther Lopez-Rivera, Scott L Friedman, Julio A Aguirre-Ghiso, Andrew G Sikora

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

34 citing papers in PubMed, 62 citations in OpenAlex.

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  17. The Role of Pre-Clinical 3-Dimensional Models of Osteosarcoma.International journal of molecular sciences · 2020
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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

6 authors at 3 institutions in 3 countries.

Michael LiDepartment of Medicine, Division of Liver Diseases, Icahn School of Medicine at Mount Sinai; Department of Otolaryngology, Icahn School of Medicine at Mount Sinai.
Ravi R PathakBobby R. Alford Department of Otolaryngology - Head and Neck Surgery, Baylor College of Medicine.
Esther Lopez-RiveraDivision of Nephrology, Columbia University College of Physicians and Surgeons.
Scott L FriedmanDepartment of Medicine, Division of Liver Diseases, Icahn School of Medicine at Mount Sinai.
Julio A Aguirre-GhisoDepartments of Medicine, Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai; julio.aguirre-ghiso@mssm.edu.
Andrew G SikoraBobby R. Alford Department of Otolaryngology - Head and Neck Surgery, Baylor College of Medicine; Andrew.Sikora@bcm.edu.
Icahn School of Medicine at Mount Sinai · USBaylor College of Medicine · USColumbia University · US

Funding

Functional Determinants of Metastatic DormancyR01CA109182 · NCI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI AGUIRRE-GHISO, JULIO A. · 2005 to 2025
$8.3M
TARGETING INOS TO INHIBIT MYELOID-DERIVED SUPPRESSOR CELLS (MDSC) IN MELANOMAK08CA154963 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SIKORA, ANDREW · 2011 to 2015
$674k
Role of Activated EGFR and COX-2 in Metastasis and Escape from Tumor DormancyR03DE021741 · NIDCR · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SIKORA, ANDREW · 2011 to 2012
$254k
Howard Hughes Medical InstituteNCI NIH HHS 1K08CA154963-01A1NCI NIH HHS K08 CA154963NCI NIH HHS R01 CA109182NIDCR NIH HHS 5R03DE021741-02NIDCR NIH HHS R03 DE021741
6 · The paper itself

Abstract

The chick chorioallantoic membrane (CAM) begins to develop by day 7 after fertilization and matures by day 12. The CAM is naturally immunodeficient and highly vascularized, making it an ideal system for tumor implantation. Furthermore, the CAM contains extracellular matrix proteins such as fibronectin, laminin, collagen, integrin alpha(v)beta3, and MMP-2, making it an attractive model to study tumor invasion and metastasis. Scientists have long taken advantage of the physiology of the CAM by using it as a model of angiogenesis. More recently, the CAM assay has been modified to work as an in vivo xenograft model system for various cancers that bridges the gap between basic in vitro work and more complex animal cancer models. The CAM assay allows for the study of tumor growth, anti-tumor therapies, and pro-tumor molecular pathways in a biologically relevant system that is both cost- and time-effective. Here, we describe the development of CAM xenograft model of hepatocellular carcinoma (HCC) with embryonic survival rates of up to 93% and reliable tumor take leading to growth of three-dimensional, vascularized tumors.

Indexed as

AnimalsCarcinoma, HepatocellularCell Line, TumorChick EmbryoChorioallantoic MembraneExtracellular Matrix ProteinsHumansLiver NeoplasmsNeoplasm TransplantationNeovascularization, PathologicXenograft Model Antitumor AssaysExtracellular Matrix Proteins

Identifiers

PMID26484588
PMCPMC4692648
OpenAlexW1810506172

What OpenQuestion holds

Textmetadata
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.