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Kategorie szczegółowe BISAC

Tumor Organoids

ISBN-13: 9783319605098 / Angielski / Twarda / 2017 / 213 str.

Shay Soker; Aleksander Skardal
Tumor Organoids Shay Soker Aleksander Skardal 9783319605098 Humana Press - książkaWidoczna okładka, to zdjęcie poglądowe, a rzeczywista szata graficzna może różnić się od prezentowanej.

Tumor Organoids

ISBN-13: 9783319605098 / Angielski / Twarda / 2017 / 213 str.

Shay Soker; Aleksander Skardal
cena 602,40
(netto: 573,71 VAT:  5%)

Najniższa cena z 30 dni: 578,30
Termin realizacji zamówienia:
ok. 22 dni roboczych.

Darmowa dostawa!

Cancer cell biology research in general, and anti-cancer drug development specifically, still relies on standard cell culture techniques that place the cells in an unnatural environment. As a consequence, growing tumor cells in plastic dishes places a selective pressure that substantially alters their original molecular and phenotypic properties.The emerging field of regenerative medicine has developed bioengineered tissue platforms that can better mimic the structure and cellular heterogeneity of in vivo tissue, and are suitable for tumor bioengineering research. Microengineering technologies have resulted in advanced methods for creating and culturing 3-D human tissue. By encapsulating the respective cell type or combining several cell types to form tissues, these model organs can be viable for longer periods of time and are cultured to develop functional properties similar to native tissues. This approach recapitulates the dynamic role of cell-cell, cell-ECM, and mechanical interactions inside the tumor. Further incorporation of cells representative of the tumor stroma, such as endothelial cells (EC) and tumor fibroblasts, can mimic the in vivo tumor microenvironment. Collectively, bioengineered tumors create an important resource for the in vitro study of tumor growth in 3D including tumor biomechanics and the effects of anti-cancer drugs on 3D tumor tissue. These technologies have the potential to overcome current limitations to genetic and histological tumor classification and development of personalized therapies.

Kategorie:
Nauka, Medycyna
Kategorie BISAC:
Medical > Oncology - General
Medical > Forensic Medicine
Wydawca:
Humana Press
Seria wydawnicza:
Cancer Drug Discovery & Development
Język:
Angielski
ISBN-13:
9783319605098
Rok wydania:
2017
Wydanie:
2018
Numer serii:
000032581
Ilość stron:
213
Waga:
0.50 kg
Wymiary:
23.39 x 15.6 x 1.42
Oprawa:
Twarda
Wolumenów:
01
Dodatkowe informacje:
Wydanie ilustrowane

Techniques to Produce and Culture Lung Tumor Organoids.- Tissue Organoids: Liver.- Mammary Gland Organoids.- Biofabrication Technologies for Developing In Vitro Tumor Models.- Three Dimensional In Vitro Tumor Platforms for Cancer Discovery.- Tissue-engineered models for studies of bone metastasis.- Building Better Tumor Models: Organoid Systems to Investigate Angiogenesis.- Microfluidics in cell and tissue studies.- Stiffness-tuned matrices for tumor cell studies.- Mathematical modeling of tumor organoids: toward personalized medicine.

Shay Soker, PhD, is Professor, Regenerative Medicine, Wake Forest Institute for Regenerative Medicine, Wake Forest School of Medicine.
Aleksander Skardal, PhD, is Assistant Professor, Regenerative Medicine and Biomedical Engineering, Wake Forest Institute for Regenerative Medicine, Wake Forest School of Medicine.

Cancer cell biology research in general, and anti-cancer drug development specifically, still relies on standard cell culture techniques that place the cells in an unnatural environment. As a consequence, growing tumor cells in plastic dishes places a selective pressure that substantially alters their original molecular and phenotypic properties.The emerging field of regenerative medicine has developed bioengineered tissue platforms that can better mimic the structure and cellular heterogeneity of in vivo tissue, and are suitable for tumor bioengineering research. Microengineering technologies have resulted in advanced methods for creating and culturing 3-D human tissue. By encapsulating the respective cell type or combining several cell types to form tissues, these model organs can be viable for longer periods of time and are cultured to develop functional properties similar to native tissues. This approach recapitulates the dynamic role of cell–cell, cell–ECM, and mechanical interactions inside the tumor. Further incorporation of cells representative of the tumor stroma, such as endothelial cells (EC) and tumor fibroblasts, can mimic the in vivo tumor microenvironment. Collectively, bioengineered tumors create an important resource for the in vitro study of tumor growth in 3D including tumor biomechanics and the effects of anti-cancer drugs on 3D tumor tissue. These technologies have the potential to overcome current limitations to genetic and histological tumor classification and development of personalized therapies.



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