Abstract

Ovarian tumors of low malignant potential (LMPs) histologically lack invasion and have excellent prognosis in contrast to invasive carcinomas. Integrins are heterodimeric adhesion molecules thought to play a role in cell migration and tumor progression. The α v β 3 integrin in particular mediates melanoma invasion in vitro and promotes neoplastic angiogenesis, facilitating breast cancer metastasis. In addition, α v β 3 expression has been detected in ovarian cancer cell lines and in a limited number of human ovarian cancer samples. The distribution pattern of this integrin in LMPs is not known. We examined tissue sections from 19 LMPs and 31 ovarian carcinomas for α v β 3 in addition to α 5 β 1 and α 2 β 1 integrins, which have been shown to be expressed in ovarian cancer cell lines. Variable immunoreactivities of α 5 β 1 and α 2 β 1 were detected in both LMPs and ovarian carcinomas. Most (74.2%) ovarian carcinomas were α v β 3 positive, whereas only 36.8% of LMPs were positive, which is statistically significant ( P = .009). These results establish the distribution pattern of α 2 β 1, α 5 β 1, and α v β 3 integrins in LMPs. The biological significance of the less frequent expression of α v β 3 in LMPs compared with carcinomas of the ovary needs further elucidation.

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