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J Clin Pathol doi:10.1136/jcp.2007.049403

Frequent nuclear expression of β-catenin protein but rare β-catenin mutation in pulmonary sclerosing hemangioma

  1. Po-Min Chiang (omicron{at}mail2000.com.tw)
  1. National Taiwan University Hospital, and College of Medicine, National Taiwan University, Taiwan
    1. Ray-Hwang Yuan (rhyuan{at}hotmail.com)
    1. National Taiwan University Hospital, and College of Medicine, National Taiwan University, Taiwan
      1. Hey-Chi Hsu (heychi{at}ntu.edu.tw)
      1. National Taiwan University Hospital, and College of Medicine, National Taiwan University, Taiwan
        1. Tsui-Lien Mao
        1. National Taiwan University Hospital, and College of Medicine, National Taiwan University, Taiwan
          1. Rey-Heng Hu
          1. National Taiwan University Hospital, and College of Medicine, National Taiwan University, Taiwan
            1. Po-Lin Lai (polin{at}ntuh.gov.tw)
            1. National Taiwan University Hospital, and College of Medicine, National Taiwan University, Taiwan
              1. Yung-Ming Jeng (d83409009{at}ntu.edu.tw)
              1. National Taiwan University Hospital, and College of Medicine, National Taiwan University, Taiwan
                • Published Online First 10 August 2007

                Abstract

                Background: Pulmonary sclerosing hemangioma (PSH) is an uncommon tumor that composed of glandular/papillary lining cells and polygonal cells. Even though the biologic behavior of this tumor has been investigated, the molecular pathogenesis of PSH was still unknown.

                Aims: To characterize the role of Wnt/β-catenin pathway in the genesis of PSH.

                Methods: 37 PSH samples were investigated by immunohistochemical detection of β-catenin protein and direct sequencing of exon 3 of β-catenin gene.

                Results: Nuclear expression of β-catenin were found in the lining component of 23 tumors (62%) and in the polygonal component of 11 tumors (30%). The expression of β-catenin was stronger in lining component, but weaker in polygonal component. Intrestingly, all the tumors with expression of β-catenin in the polygonal component also expressed β -catenin in the lining component. But mutation of exon 3 of β-catenin gene was detected in only one tumor that expressed nuclear β-catenin in both lining and polygonal components.

                Conclusions: Wnt/β-catenin pathway was involved in genesis of PSH , but mutation of exon 3 of -βcatenin gene rarely contributed to the activation of Wnt/β-catenin pathway in PSH.

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