TY - JOUR
T1 - c-myc, c-erbb-2, c-fms and bcl-2 Oncoproteins
T2 - Expression in normal placenta, partial and complete mole, and choriocarcinoma
AU - Fulop, Vilmos
AU - Mok, Samuel C.
AU - Genest, David R.
AU - Szigetvari, Ivan
AU - Cseh, Imre
AU - Berkowitz, Ross S.
N1 - Copyright:
Copyright 2012 Elsevier B.V., All rights reserved.
PY - 1998/2
Y1 - 1998/2
N2 - OBJECTIVE: To determine the expression of bcl-2, c-myc, c-fms and c- erbB-2 oncoproteins in normal placentas, partial and complete hydatidiform moles, and choriocarcinomas and to examine the possible presence of mutations in the K-ras gene in complete moles and choriocarcinomas. STUDY DESIGN: The expression of the above oncoproteins was determined immunohistochemically by specific antibodies for these proteins on formalin-fixed paraffin sections of 18 normal placentas, 17 partial moles, 25 complete moles and 11 choriocarcinomas. This was followed by polymerase chain reaction analysis (exons 12 and 13) of K-ras gene for possible mutations in complete moles and choriocarcinomas. RESULTS: Expression of c fms oncoprotein appeared confined to the cytoplasm of syncytiotrophoblastic cells. The c-fms protein staining intensity of the syncytiotrophoblastic layer showed no significant difference among the four gestational tissues. c-erbB-2 antibody expression was confined to the cellular membrane of the extravillous trophoblast. When compared with normal placenta or partial mole, the expression of c-erbB-2 protein was significantly stronger in complete mole (P <.0001 and P<.0001, respectively) and choriocarcinoma (P<.0001 and P<.0001, respectively). Expression of bcl-2 protein was significantly stronger in the syncytiotrophoblast in complete mole and choriocarcinoma as compared to both normal placenta and partial mole (P<.0001 and P<.0001, respectively) Staining of c-myc of the syncytiotrophoblastic layer was significantly stronger in placenta, complete mole and choriocarcinoma than in partial mole (P <.0001, P <. 0001 and P <.0001, respectively). Mutation in K-ras gene was not found in any of the 22 complete moles or 11 choriocarcinomas examined. CONCLUSION: Our data suggest that c-myc, c-erbB-2, c-fins and bcl-2 oncoproteins may be important in the pathogenesis of complete mole and choriocarcinoma. However, while both complete mole and choriocarcinoma were characterized by overexpression of c- myc, c-erbB-2 and bcl-2, partial mole generally did not strongly express these three oncoproteins.
AB - OBJECTIVE: To determine the expression of bcl-2, c-myc, c-fms and c- erbB-2 oncoproteins in normal placentas, partial and complete hydatidiform moles, and choriocarcinomas and to examine the possible presence of mutations in the K-ras gene in complete moles and choriocarcinomas. STUDY DESIGN: The expression of the above oncoproteins was determined immunohistochemically by specific antibodies for these proteins on formalin-fixed paraffin sections of 18 normal placentas, 17 partial moles, 25 complete moles and 11 choriocarcinomas. This was followed by polymerase chain reaction analysis (exons 12 and 13) of K-ras gene for possible mutations in complete moles and choriocarcinomas. RESULTS: Expression of c fms oncoprotein appeared confined to the cytoplasm of syncytiotrophoblastic cells. The c-fms protein staining intensity of the syncytiotrophoblastic layer showed no significant difference among the four gestational tissues. c-erbB-2 antibody expression was confined to the cellular membrane of the extravillous trophoblast. When compared with normal placenta or partial mole, the expression of c-erbB-2 protein was significantly stronger in complete mole (P <.0001 and P<.0001, respectively) and choriocarcinoma (P<.0001 and P<.0001, respectively). Expression of bcl-2 protein was significantly stronger in the syncytiotrophoblast in complete mole and choriocarcinoma as compared to both normal placenta and partial mole (P<.0001 and P<.0001, respectively) Staining of c-myc of the syncytiotrophoblastic layer was significantly stronger in placenta, complete mole and choriocarcinoma than in partial mole (P <.0001, P <. 0001 and P <.0001, respectively). Mutation in K-ras gene was not found in any of the 22 complete moles or 11 choriocarcinomas examined. CONCLUSION: Our data suggest that c-myc, c-erbB-2, c-fins and bcl-2 oncoproteins may be important in the pathogenesis of complete mole and choriocarcinoma. However, while both complete mole and choriocarcinoma were characterized by overexpression of c- myc, c-erbB-2 and bcl-2, partial mole generally did not strongly express these three oncoproteins.
KW - Choriocarcinoma
KW - Mole
KW - Oncoproteins
KW - Ras genes
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M3 - Article
C2 - 9513871
AN - SCOPUS:0031915860
SN - 0024-7758
VL - 43
SP - 101
EP - 110
JO - Journal of Reproductive Medicine for the Obstetrician and Gynecologist
JF - Journal of Reproductive Medicine for the Obstetrician and Gynecologist
IS - 2
ER -