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Volume 3

Diagnostic Pathology: Open Access

ISSN: 2476-2024

Laboratory Medicine 2018

June 25-26, 2018

June 25-26, 2018 | Berlin, Germany

13

th

International Conference on

Laboratory Medicine & Pathology

Combining 2D angiogenesis and 3D osteosarcoma microtissues to improve vascularization

Hassan Chaddad

INSERM, UMR 1260, Regenerative Nanomedicine, FMTS, University of Strasbourg, France

Introduction:

The number of patients suffering from cancers worldwide is increasing, and one of the most challenging issues

in oncology continues to be the problem of developing active drugs economically and in a timely manner. Considering the high

cost and time-consuming nature of the clinical development of oncology drugs, better pre-clinical platforms for drug screening

are urgently required. So, there is need for high-throughput drug screening platforms to mimic the

in vivo

microenvironment.

Angiogenesis is now well known for being involved in tumour progression, aggressiveness, emergence of metastases, and also

resistance to cancer therapies.

Materials & Methodology:

In this study, to better mimic tumour angiogenesis encountered

in vivo

, we used 3D culture of

osteosarcoma cells (MG-63) that we deposited on 2D endothelial cells (HUVEC- Human Umbilical vein Endothelial Cells)

grown in monolayer. Combination 2D HUVEC/3D MG-63 was characterized by Indirect immunofluorescence, Scanning

electron microscopy, Optical microscopy and mRNA expression (qPCR).

Results:

We reported that endothelial cells combined with tumor cells were able to form a well-organized network, and those

tubule-like structures corresponding to new vessels infiltrate tumor spheroids. These vessels presented a lumen and expressed

specific markers as CD31 and collagen IV. The combination of 2D endothelial cells and 3D microtissues of tumor cells also

increased expression of angiogenic factors as VEGF, CXCR4 and ICAM1.

Conclusions:

The cell environment is the key point to develop tumor vascularization

in vitro

and to be closer to tumor

encountered

in vivo

.

Hassan.chaddad@unistra.fr

Diagn Pathol Open 2018, Volume 3

DOI: 10.4172/2476-2024-C1-003