PAPILLARY CYSTIC TUMORS OF THE PANCREAS - ASSESSMENT OF MALIGNANT POTENTIAL BY ANALYSIS OF PROGESTERONE-RECEPTOR, FLOW-CYTOMETRY, AND RAS ONCOGENE MUTATION
Wy. Lee et al., PAPILLARY CYSTIC TUMORS OF THE PANCREAS - ASSESSMENT OF MALIGNANT POTENTIAL BY ANALYSIS OF PROGESTERONE-RECEPTOR, FLOW-CYTOMETRY, AND RAS ONCOGENE MUTATION, Anticancer research, 17(4A), 1997, pp. 2587-2591
Background Although the biologic behavior of papillary cystic armor (P
CT) of the pancreas is more favorable than the adenocarcinoma, a malig
nant form has been reported. There has been much controversy as to the
histologic evidence for malignancy. The purpose of this study is to e
valuate whether the ras oncogene mutation is present in the PCT, toget
her with hormone receptor status and DNA flow cytometry that can be us
ed to predict armor aggressiveness. Materials and Methods. In 6 collec
ted cases of PCT, estrogen receptors (ER) and progesterone receptors (
PR) were detected by immunohistochemical techniques, DNA ploidy and S-
phase fr action (SPF) were studied by flow cytometry, and H, K and N-r
as oncogene mutation were analyzed by polymerase chain reaction (PCR).
Results. General strong positive immunostaining of PR and negative st
aining of ER are found in all 6 cases of PCT, including 5 adolescent g
irls and one 55-year-old women with areas of anaplastic transformation
. Flow cytometry analysis revealed diploid DNA in all 6 cases but high
er SPF in the anaplastic portion of the old one. None of the 6 cases s
howed H-, K-, or N-ras oncogene mutation. Conclusions. These results s
uggest PR status and ras oncogene mutation appear to be nor useful in
predicting aggressive behavior: DNA ploidy and S-phase fraction may pr
ovide useful information for prognosis, but their more precise prognos
tic value of PCT needs a larger number of cases to clarify.