How best to identify p53 abnormalities in prostate cancer - Increasing attention is being paid
to determining abnormal mutants of human chromosomes, such as the tumor-suppressing p53 in
human cancers, as a possible guide to prognosis and treatment. Before reliance is placed on
such genetic indicators however, we must be very sure of two things - the best way to identify
these abnormalities, and of what exactly the alterations imply for the patient. An article in the
January 1, 1997 issue of the Journal of the National Cancer Institute by the Cooperative Prostate
Network in the US concluded that a combination of two measurements is necessary to identify
all the possible p53 changes. Both tests are based on what is known as the polymerase chain
reaction (PCR), but one starts from DNA (DNA-PCR-SSCP), while the other starts from RNA
(ribonucleic acid) which is converted to its corresponding DNA before PCR is carried out (TR-PCR-SSCP). This is because many cancers contain more than one altered p53 gene. This
situation may apply also to tumors other than prostate cancer. (Gumerlock, J Nat Cancer Inst
89:66, 1997)
Editor's Comment: - p53 measurements more typically look at the protein product by
immunologic methods rather than the specific mutations that may be present. It is interesting
that a short report from a group of researchers in University College, Dublin, Ireland (Leahy, J Pathol 180:364, December, 1996) also concluded that measurement of overexpressed p53
protein was a better guide to identifying high-risk colorectal patients than was determination
of specific mutations by PCR-SSCP, which showed no relationship to outcome.