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[Cancer Research 61, 4536-4540, June 1, 2001]
© 2001 American Association for Cancer Research


Regular Articles

Detection of Differentially Expressed Genes in HeLa x Fibroblast Hybrids Using Subtractive Suppression Hybridization1

Satoshi Nishizuka2, Hiroyuki Tsujimoto3 and Eric J. Stanbridge

Department of Microbiology and Molecular Genetics, College of Medicine, University of California, Irvine, Irvine, California 92697-4025

To understand genetic differences and similarities between tumorigenic and nontumorigenic HeLa x fibroblast hybrid cells, subtractive suppression hybridization (SSH), based on suppression PCR and a combination of normalization and subtraction in a single procedure, was used. Using the nontumorigenic CGL1 and tumorigenic CGL3, forward (CGL1-CGL3) and reverse (CGL3-CGL1) subtracted libraries were constructed. Among 192 clones, seven were identified as differentially expressed genes specific for either CGL1 or CGL3. All seven were not reported previously as differentially expressed genes in this hybrid system. In the forward subtraction, p16 was isolated, indicating the involvement of the loss of tumorigenic phenotype. Subsequent transfection of wild-type p16 to the tumorigenic CGL3 showed growth suppression in colony formation assay; however, no tumor suppression was observed when the transfectant was inoculated into nude mice. These results indicate that: (a) SSH is a suitable method to identify differentially expressed genes in two types of cells; and (b) although p16 plays some roles in growth suppression, the p16-transfected CGL3 is still capable to proliferate in vivo.




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D. von Bubnoff, H. Matz, J.-P. Cazenave, D. Hanau, T. Bieber, and H. de la Salle
Kinetics of Gene Induction After Fc{epsilon}RI Ligation of Atopic Monocytes Identified by Suppression Subtractive Hybridization
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[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
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Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2001 by the American Association for Cancer Research.