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Cell
Volume 29, Issue 1, May 1982, Pages 161-169
 
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doi:10.1016/0092-8674(82)90100-3    
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Copyright © 1982

Article

Isolation of a transforming sequence from a human bladder carcinoma cell line

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Chiaho Shih* and Robert A. Weinberg

Center for Cancer Research and Department of Biology Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA


Received 11 January 1982; 
Revised 19 February 1982. 
Available online 29 April 2004.

Abstract

We have isolated the component of human bladder carcinoma cell DNA that is able to transform mouse fibroblasts. The oncogenic sequence was isolated initially from a lambda phage genomic library made from DNA of a transfected mouse cell carrying the human oncogene. A subcloned insert of 6.6 kb that carried transforming activity was amplified in the plasmid vector pBR322. The subcloned oncogene has been used as a sequence probe in Southern blot analyses. The oncogene appears to derive from sequences present in normal cellular DNA. Structural analysis has failed so far to reveal differences between the oncogene and its normal cellular homolog. The oncogene is unrelated to transforming sequences detected in a variety of other types of human tumor cell lines derived from colonic and lung carcinoma and from neuroblastoma. In contrast, the EJ bladder oncogene appears closely related to one that is active in the human T24 bladder carcinoma cell line. The oncogene appears to have undergone little, if any, amplification in several bladder carcinoma cell lines.

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* Present address: Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts 02114.


Cell
Volume 29, Issue 1, May 1982, Pages 161-169
 
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