Kr. Mittal et al., CERVICAL SQUAMOUS DYSPLASIAS AND CARCINOMAS WITH IMMUNODETECTABLE P53FREQUENTLY CONTAIN HPV, Gynecologic oncology, 58(3), 1995, pp. 289-294
Studies using cervical carcinoma cell lines usually show mutated p53 i
n cases without detectable HPV, and wild-type p53 in cases with detect
able HPV. These findings suggest that loss of p53 function, either by
mutation or by binding to HPV E6, is required for cervical carcinogene
sis. Because mutated p53 is usually detectable immunohistochemically,
one would predict an inverse relationship between the presence of HPV
and detectable p53. In this study we examined 88 formalin-fixed paraff
in-embedded clinical specimens of cervix for the presence of HPV and p
53 expression. All cases were studied for the presence of p53 using im
munohistochemical methods. The antibody used was mouse monoclonal PAb1
801 (Biogenex). The presence of HPV was detected by PCR. Twenty-six sp
ecimens showed foci of p53 expression (0/7 normal, 1/8 (13%) condyloma
s, 1/6 (17%) CIN I, 3/7 (43%) CIN II, 6/ 20 (30%) CIN III, 13/22 (59%)
SCC, 2/5 (40%) adenosquamous carcinomas, and 0/13 adenocarcinomas). p
53 expression was more frequent in SCC than with CIN (P = 0.026). HPV
was present in 15 of 24 cases with detectable p53 and 22 of 48 cases w
ithout detectable p53. No correlation was seen between HPV status and
detection of p53. With the exception of one case, p53 expression was s
een in less than 10% of cells. p53 expression was not detected in any
of the 13 adenocarcinomas examined (P = 0.0016 vs SCC). Our results sh
ow that alterations of p53 may play a role in the pathogenesis of cerv
ical squamous carcinoma However, p53 expression was neither sufficient
nor required for cervical carcinogenesis, irrespective of HPV status.
(C) 1995 Academic Press Inc.