Frequency of p53, p21Waf1, and p16INK4a Gene Alterations and Expression in MCLs
Diagnosis . | p53 Mutations . | p21Waf1 . | p16INK4a . | ||||
---|---|---|---|---|---|---|---|
MCL Variant . | . | Deletions . | Mutational Analysis . | Loss of Expression . | Deletions . | Mutational Analysis . | Loss 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 |
Diagnosis . | p53 Mutations . | p21Waf1 . | p16INK4a . | ||||
---|---|---|---|---|---|---|---|
MCL Variant . | . | Deletions . | Mutational Analysis . | Loss of Expression . | Deletions . | Mutational Analysis . | Loss 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.