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Immunohistochemical analysis of c-erbB-2, Bcl-2, p53, p21WAF1/Cip1, p63 and Ki-67 expression in hydatidiform moles
Authors:Nabiha Missaoui  Hanene Landolsi  Sarra Mestiri  Ahlem Essakly  Nihed Abdessayed  Sihem Hmissa  Moncef Mokni  Mohamed Tahar Yacoubi
Affiliation:1. Research Unit UR14ES17, Cancer Epidemiology and Cytopathology in Tunisian Center, Medicine Faculty of Sousse, University of Sousse, 4000 Sousse, Tunisia;2. Faculty of Sciences and Techniques, Sidi Bouzid, Kairouan University, Tunisia;3. Pathology Department, Farhet Hached Hospital, 4000 Sousse, Tunisia;4. Medicine Faculty of Sousse, University of Sousse, 4000 Sousse, Tunisia
Abstract:Hydatidiform moles (HM) are characterized by an abnormal proliferating trophoblast with a potential for a malignant transformation. Similar to other human tumors, trophoblastic pathogenesis is likely a multistep process involving several molecular and genetic alterations. The study was performed to investigate the expression patterns of c-erbB-2 and Bcl-2 oncoproteins, p53, p21WAF1/CIP1 and p63 tumor suppressor proteins and Ki-67 cell proliferation marker in HM.We conducted a retrospective study of 220 gestational products, including 39 hydropic abortions (HA), 41 partial HM (PHM) and 140 complete HM (CHM). The expression of c-erbB-2, Bcl-2, p53, p21WAF1/CIP1, p63 and Ki-67 was investigated by immunohistochemistry on archival tissues. c-erbB-2 expression was observed in three PHM and 10 CHM. Bcl-2 immunostaining was significantly higher in PHM (61%) and CHM (70.7%) compared with HA (7.7%, p?=? 0.001 and p?p < 0.0001) and HA (12.8%, p < 0.0001). p21WAF1/CIP1 staining was observed as well in molar and non-molar gestations (p?>? 0.05). p63 immunoexpression was significantly described in CHM (85.7%) and PHM (78%) compared with HA (10.2%, p < 0.0001 and p = 0.0001, respectively). Ki-67 was significantly expressed in CHM (72.1%) compared with HA (46.2%, p = 0.005).Altered expression of Bcl-2, p53, p63 and Ki-67 reflects the HM pathological development. Immunohistochemical analysis is beneficial to recognize the HM molecular and pathogenic mechanisms. Furthermore, it could serve as a useful adjunct to conventional methods for refining HM diagnosis.
Keywords:CHM  complete hydatidiform moles  HA  hydropic abortions  HM  hydatidiform moles  GTD  gestational trophoblastic disease  GTN  gestational trophoblastic neoplasia  PHM  partial hydatidiform moles  Complete hydatidiform mole  Partial hydatidiform mole  Hydropic abortion  Bcl-2  p53  p63  Ki-67
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