Cancer Cell Lines Part 2 edited by John Masters, Bernhard Ø Palsson.

Continuous cell lines derived from human cancers are the mostwidely used resource in laboratory-based cancer research. The first 3 volumes of this series on Human Cell Culture are devoted to these cancer cell lines. The chapters in these first 3 volumes have a common aim. Their purpose is to address...

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Bibliographic Details
Corporate Author: SpringerLink (Online service)
Other Authors: Masters, John (Editor), Palsson, Bernhard Ø. (Editor)
Format: eBook
Language:English
Published: Dordrecht : Springer Netherlands : Imprint: Springer, 2002.
Edition:1st ed. 2002.
Series:Human Cell Culture, 2
Springer eBook Collection.
Subjects:
Online Access:Click to view e-book
Holy Cross Note:Loaded electronically.
Electronic access restricted to members of the Holy Cross Community.

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505 0 |a Ovarian Cancer -- Cervical Cancer -- Endometrial Cancer -- Breast Cancer -- Paired Breast Cancer Cell Lines -- Ovarian Germ Cell Tumors -- Testicular Germ Cell Tumors -- Choriocarcinoma -- Thymomas and Thymic Cancers -- Kaposi’s Sarcoma -- Brain Tumors -- Head and Neck Cancers -- Gastric Cancer -- Colorectal Cancer -- Prostate Cancer -- Liver Cancer -- Wilms’ Tumor and Other Childhood Renal Neoplasms -- Retinoblastoma. 
520 |a Continuous cell lines derived from human cancers are the mostwidely used resource in laboratory-based cancer research. The first 3 volumes of this series on Human Cell Culture are devoted to these cancer cell lines. The chapters in these first 3 volumes have a common aim. Their purpose is to address 3 questions offundamental importance to the relevanceof human cancer cell lines as model systems of each type of cancer: 1. Do the cell lines available accurately represent the clinical presentation? 2. Do the cell lines accurately represent the histopathology of the original tumors? 3. Do the cell lines accurately represent the molecular genetics of this type of cancer? The cancer cell lines available are derived, in most cases, from the more aggressive and advanced cancers. There are few cell lines derived from low grade organ-confined cancers. This gap can be filled with conditionally immortalized human cancer cell lines. We do not know why the success rate for establishing cell lines is so low for some types of cancer and so high for others. The histopathology of the tumor of origin and the extent to which the derived cell line retains the differentiated features of that tumor are critical. The concept that a single cell line derived from a tumor at a particular site is representative oftumors at that site is naïve and misleading. 
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