Table 1.

Frequency of p53, p21Waf1, and p16INK4a Gene Alterations and Expression in MCLs

Diagnosisp53 Mutationsp21Waf1p16INK4a
MCL VariantDeletionsMutational AnalysisLoss of ExpressionDeletionsMutational AnalysisLoss of Expression
Aggressive 2/6 0/5 0/5 1/6 3/6* 0/3 2/5 
Typical 0/18 0/18 1/18 0/18 0/18 1/18 0/17 
 
Total 2/24 0/23 1/23 1/24 3/24 1/21 2/22 
Diagnosisp53 Mutationsp21Waf1p16INK4a
MCL VariantDeletionsMutational AnalysisLoss of ExpressionDeletionsMutational AnalysisLoss of Expression
Aggressive 2/6 0/5 0/5 1/6 3/6* 0/3 2/5 
Typical 0/18 0/18 1/18 0/18 0/18 1/18 0/17 
 
Total 2/24 0/23 1/23 1/24 3/24 1/21 2/22 
*

Two cases showed homozygous deletions by Southern blot analysis. One additional case had a hemizygous deletion of the 9p −del (9) (p12)−. No DNA was available in this case.

The SSCP analysis was not performed in the cases with homozygous p16INK4a gene deletion.

The two cases with anomalous SSCP had a known polymorphism in codons 31 of p21Waf1 gene and codon 148 of p16INK4a gene, respectively.

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