Human Cell Culture: Cancer Cell Lines Part 2 by Anne P. Wilson, Chris M. Garner (auth.), John R. W. Masters,

By Anne P. Wilson, Chris M. Garner (auth.), John R. W. Masters, Bernhard Palsson (eds.)

Continuous mobile strains derived from human cancers are the mostwidely used source in laboratory-based melanoma examine. the 1st three volumes of this sequence on Human telephone tradition are dedicated to those melanoma mobile strains. The chapters in those first three volumes have a typical target. Their objective is to handle three questions offundamental significance to the relevanceof human melanoma mobilephone strains as version structures of every kind of melanoma: 1. Do the mobile strains to be had correctly symbolize the scientific presentation? 2. Do the mobile traces effectively symbolize the histopathology of the unique tumors? three. Do the mobilephone traces effectively characterize the molecular genetics of this sort of melanoma? The melanoma cellphone traces on hand are derived, mostly, from the extra competitive and complicated cancers. There are few telephone strains derived from low grade organ-confined cancers. This hole should be choked with conditionally immortalized human melanoma phone traces. we don't be aware of why the good fortune cost for constructing telephone traces is so low for a few varieties of melanoma and so excessive for others. The histopathology of the tumor of starting place and the level to which the derived cellphone line keeps the differentiated beneficial properties of that tumor are serious. the idea that a unmarried cellphone line derived from a tumor at a specific web site is consultant oftumors at that web site is naïve and misleading.

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Nonclonogenic in agar Epithelial-like monolayer. Doubling time 74 hours. PE 1% in agar Nk Adherent monolayer. Doubling time 151 hours Adherent monolayer Adherent monolayer Epithelial-like monolayer In vitro features of cell line Nk Nk Nk Nk Nk Nk Nk Nk Nk Nk Continued on next page Nk Undifferentiated carcinoma in nude mice. Xenograft model. SC/Solid Six of 14 formed tumors in nude mice SC/Cystic and solid tumors with vascular invasion. Adherent monolayer Adherent epithelial-like monolayer Continued on next page Tumors in immunosuppressed mice.

Clamon G et al. Gynecologic Oncology 20: 92, 1985. Benard J et al. Cancer Research 45: 4970, 1985. Hill BT et al. International Journal of Cancer 39: 219, 1987. Riken _ Unpublished data. Deposited by Nishi and Yoshiro. Sasa H et al. Human Cell 6: 106, 1993. Morimitsu Y et al. Gynecologic Oncology 48: 155, 1993. Motayama T,Acta Obstet Gynecol Jpn 33: 1197, 1981. Hirte HW et al. Cancer 74: 900, 1994. Kidera Y et al. Acta Obst Gynaec Jpn 37: 1820, 1985. Miyagi E et al. Clinical & Experimental Metastasis 13: 89, 1995.

11. 12. 13. 14. 15. Boyle P et al. In Ovarian Cancer 4, Pub. Chapman and Hall, Chapter 9: 91, 1996. Southam CM, Cancer; 7, 394, 1954. Rose GG et al. Journal of the National Cancer Institute 11: 1223, 1951. Wright JC et al. Cancer 15: 284, 1962. Limburg HG, Proc Roy Soc Med 62: 361, 1969. Ioachim HL et al. Laboratory Investigation 31: 381, 1974. Ioachim HL et al. Natl Cancer Inst Monogr 42: 45, 1975. DiSaia PJ et al. Gynecologic Oncology 3: 215, 1975. Acta Path Jap 25: 89, 1975. Wilson AP, In Cell and Tissue Culture Laboratory Procedures, John Wiley and Sons, Preparation of Ovarian Cell Cultures, 1996.

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