Session

S02 3D in vitro tissue-engineered cancer/disease models – Session II

S02
Jun 28, 2022, 1:30 PM
ICE Krakow

ICE Krakow

ul. Marii Konopnickiej 17 30-302 Kraków

Conveners

S02 3D in vitro tissue-engineered cancer/disease models – Session II

  • Rui L. Reis
  • Serena Danti

Presentation materials

There are no materials yet.

  1. Prakash, Jai (University of Twente)
    6/28/22, 1:30 PM
    invited lecture

    "Introduction: Pancreatic ductal adenocarcinoma (PDAC) is one of the most fibrotic tumors, which can possess up to 90% tumor stroma of the total tumor mass (1). The tumor stroma is comprised of cancer-associated fibroblasts (CAFs), extracellular matrix (ECM) and many immune cells. The physical and biochemical characteristics of the tumor stroma control cancer cell proliferation, invasion, and...

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  2. Rousselle, Adrien (Inserm UMR 1121 )
    6/28/22, 1:50 PM
    podium presentation

    Extrusion bio-printing is the most direct and inexpensive method for printing three-dimensional cell models. This technique provides interesting solutions to generate more complex architectures than the already existing 3D models but still presents significant drawbacks that once solved will improve its field of application in regenerative medicine and advanced 3D biological models. To print...

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  3. Neagu, Adrian (Victor Babes University of Medicine and Pharmacy Timisoara )
    6/28/22, 2:00 PM
    podium presentation

    Understanding the key players in cancer progression is essential for the development of effective therapies. Aiming to pinpoint the roles of biochemical and biophysical factors involved in malignancy, tissue engineers developed in vitro cancer models of increasing complexity [1]. Three-dimensional (3D) bioprinting techniques were extensively used in this endeavor [2,3] due to their ability to...

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  4. Urbani, Luca (Roger Williams Institute of Hepatology )
    6/28/22, 2:10 PM
    podium presentation

    Introduction: Current primary liver cancer models fail to truly encompass the human tumour immune microenvironment, exacerbating a recognised discord between the preclinical and clinical successes of emerging (immuno)therapeutics. The organotypic 3D culture of human precision-cut tumour slice (PCTS) is a cancer explant model which retains tumour specific histoarchitecture, aetiological...

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  5. Blanco-Fernandez, Barbara (Institute for Bioengineering of Catalonia (IBEC) )
    6/28/22, 2:20 PM
    podium presentation

    Introduction
    3D bioprinting has emerged as a promising technology for fabricating artificial tumors as it allows the fabrication of complex models recreating tumor physiology. The importance of the extracellular matrix (ECM) in tumor progression, cancer cells and stromal cells crosstalk and drug resistances, has motivated the development of more biomimetic tumor-ECM bioinks that recapitulate...

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  6. Sainsbury, Elizabeth (Royal College of Surgeons Ireland )
    6/28/22, 2:30 PM
    podium presentation

    Treatment options for triple-negative breast cancer (TNBC) are limited. Current 2D cancer models fail to accurately model the tumour microenvironment of breast cancer. Alterations to extracellular matrix (ECM) composition have been shown to play a key role in the epithelial-mesenchymal transition (EMT) process involved in breast cancer progression (1). This highlights the need for the...

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  7. Ozturk, Ece (Koc University )
    6/28/22, 2:40 PM
    podium presentation

    Introduction
    Lung cancer is the leading cause of cancer mortality with poor prognosis due to late stage diagnosis, drug resistance and high risk of relapse. There is a high need for tissue engineered 3D models that can recapitulate tumor heterogeneity and complexity to understand the cellular mechanisms leading to lung tumorigenesis, metastasis and drug responses. Future of precision oncology...

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  8. Micalet, Auxtine (University College London )
    6/28/22, 2:50 PM
    podium presentation

    INTRODUCTION: Most epithelial cancer cell populations undergo an epithelial to mesenchymal transition (EMT), acquiring a more aggressive phenotype1. Mesenchymal cells are more motile and have the ability to remodel the extracellular matrix. This mechanical interaction with the surrounding matrix can be measured by bulk and single cell force generation. In this study we aim to use 3D in vitro...

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