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The importance of circulating tumor cells and tumor models in future of cancer therapy

The importance of circulating tumor cells and tumor models in future of cancer therapy
The importance of circulating tumor cells and tumor models in future of cancer therapy
Development of new technologies is taking cancer research on a new journey in which plenty of mysterious aspects of cancer biology are being unraveled. To defeat cancer, we first need to understand the biology of this smart complex system, which often hijacks several programs to proliferate, invade, escape the immune system and colonize distant organs. Therefore, studying cancer cells in every step of tumor development (including primary tumor formation, invasion, circulation and metastatic colonization) is absolutely essential. Analysis of human-derived cancer models in primary site, circulation or metastatic lesions outside their host is one of the most promising ways to understand these complexities. The most common currently used and more recently developed cancer cell lines consist of primary patient-derived tumor xenograft (PDTX), circulating tumor cells isolation and analyzes, and primary tumor organoids. In this chapter we provide a brief update of some of the most important advances in studying and treatment of cancer using new technologies
article, cancer growth, cancer research, cancer resistance, cancer therapy, circulating tumor cell, human, immune deficiency, microfluidic analysis, nonhuman, protein expression, tumor escape, tumor microenvironment, tumor model, tumor xenograft
2196-9914
121-135
Humana
Behnam, B.
bb3a7da7-42d7-40c0-ac86-18bdecb71732
Fazilaty, H.
d9c7bf1b-abd3-44cb-9e78-2984037ea9d9
Roghanian, A.
e2b032c2-60a0-4522-a3d8-56a768792f36
Aref, A.
Barbie, D.
Behnam, B.
bb3a7da7-42d7-40c0-ac86-18bdecb71732
Fazilaty, H.
d9c7bf1b-abd3-44cb-9e78-2984037ea9d9
Roghanian, A.
e2b032c2-60a0-4522-a3d8-56a768792f36
Aref, A.
Barbie, D.

Behnam, B., Fazilaty, H. and Roghanian, A. (2017) The importance of circulating tumor cells and tumor models in future of cancer therapy. In, Aref, A. and Barbie, D. (eds.) Ex Vivo Engineering of the Tumor Microenvironment. (Cancer Drug Discovery and Development (CDD&D)) Cham. Humana, pp. 121-135. (doi:10.1007/978-3-319-45397-2_7).

Record type: Book Section

Abstract

Development of new technologies is taking cancer research on a new journey in which plenty of mysterious aspects of cancer biology are being unraveled. To defeat cancer, we first need to understand the biology of this smart complex system, which often hijacks several programs to proliferate, invade, escape the immune system and colonize distant organs. Therefore, studying cancer cells in every step of tumor development (including primary tumor formation, invasion, circulation and metastatic colonization) is absolutely essential. Analysis of human-derived cancer models in primary site, circulation or metastatic lesions outside their host is one of the most promising ways to understand these complexities. The most common currently used and more recently developed cancer cell lines consist of primary patient-derived tumor xenograft (PDTX), circulating tumor cells isolation and analyzes, and primary tumor organoids. In this chapter we provide a brief update of some of the most important advances in studying and treatment of cancer using new technologies

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More information

e-pub ahead of print date: 10 December 2016
Published date: 2017
Keywords: article, cancer growth, cancer research, cancer resistance, cancer therapy, circulating tumor cell, human, immune deficiency, microfluidic analysis, nonhuman, protein expression, tumor escape, tumor microenvironment, tumor model, tumor xenograft

Identifiers

Local EPrints ID: 413399
URI: http://eprints.soton.ac.uk/id/eprint/413399
ISSN: 2196-9914
PURE UUID: 7f1a88fc-f9fc-49de-97cc-79f5bcc34951
ORCID for A. Roghanian: ORCID iD orcid.org/0000-0003-1316-4218

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Date deposited: 23 Aug 2017 16:32
Last modified: 16 Mar 2024 04:01

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Contributors

Author: B. Behnam
Author: H. Fazilaty
Author: A. Roghanian ORCID iD
Editor: A. Aref
Editor: D. Barbie

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