G. Zalcman et al., MONITORING OF P53 AUTOANTIBODIES IN LUNG-CANCER DURING THERAPY - RELATIONSHIP TO RESPONSE TO TREATMENT, Clinical cancer research, 4(6), 1998, pp. 1359-1366
Alteration of the p53 gene is the most frequent genetic alteration in
human cancer, and it leads to the accumulation of mutant p53 in the nu
cleus of tumor cells, In addition, it has been shown that patients wit
h various types of neoplasias have p53 antibodies in their sera. ELISA
was used to detect anti-p53 antibodies in the sera of 167 patients wi
th lung cancer. Among these, 32 individuals (16 positive for p53 antib
odies and 16 negative) were monitored over a period of 30 months for p
53 antibodies. Twelve of 16 antibody positive patients had reduced tit
ers during chemotherapy that led to partial or complete remissions of
disease. The specificity of these antibodies was confirmed by two diff
erent ELISA procedures and by immunoprecipitation, The very rapid, spe
cific decrease in these antibodies during therapy suggests that a cons
tant level of tumoral cells with nuclear accumulating p53 protein is n
ecessary for a detectable humoral anti-p53 response. The good correlat
ion found between the specific evolution of the p53 antibody titer and
the response to therapy suggests that p53 antibodies could represent
a useful tool for checking the response to therapy and for monitoring
some relapses before they are clinically detectable.