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Stromal nitric oxide synthase (NOS) expression correlates with the grade of mammary phyllodes tumour
  1. G M K Tse1,
  2. F C Wong1,
  3. A K H Tsang1,
  4. C S Lee5,
  5. P C W Lui3,
  6. A W I Lo1,
  7. B K B Law2,
  8. R A Scolyer5,
  9. R Z Karim5,
  10. T C Putti4
  1. 1Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, Chinese University of Hong Kong, Ngan Shing Street, Shatin, NT, Hong Kong, China
  2. 2Department of Surgery, Prince of Wales Hospital, Chinese University of Hong Kong
  3. 3Department of Pathology, United Christian Hospital, Kwan Tong, Kowloon, Hong Kong, China
  4. 4Department of Pathology, National University Hospital, 5 Lower Kent Ridge Road, Singapore, 119074
  5. 5Department of Pathology, University of Sydney, and Department of Anatomical Pathology, Royal Prince Alfred Hospital, Sydney, 2050 Australia
  1. Correspondence to:
 Dr G M Tse
 Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, Ngan Shing Street, Shatin, NT, Hong Kong, China; garytsecuhk.edu.hk

Abstract

Background: Nitric oxide synthase (NOS), particularly endothelial and inducible forms (e/i-NOS), are expressed in various cancers, including breast cancer. In mammary fibroepithelial lesions, NOS expression in stromal cells has been reported to be lower in fibroadenomas than in phyllodes tumours.

Aims: To investigate NOS expression in phyllodes tumours of varying degrees of malignancy.

Methods: One hundred and sixty seven mammary phyllodes tumours (97 benign, 47 borderline malignant, and 23 frankly malignant) were evaluated for e-NOS and i-NOS expression by immunohistochemistry. Correlations with previously reported expression of stromal vascular growth factor (VEGF) and microvessel density were also performed.

Results: Stromal expression of e-NOS was absent, weak, moderate, and strong in 43%, 31%, 13%, and 13% of benign tumours; 17%, 26%, 13%, and 44% of borderline malignant tumours; and 17%, 35%, 13%, and 35% of frankly malignant tumours, respectively. Stromal expression of i-NOS was 77%, 18%, 4%, and 1% in benign tumours; 42%, 28%, 19%, and 11% in borderline malignant tumours; and 43%, 13%, 26%, and 18% in frankly malignant tumours, respectively. Stromal expression of both i-NOS and e-NOS was significantly different between the benign and malignant (borderline and frank) groups of phyllodes tumours (p<0.0001). Furthermore, the expression of i-NOS correlated with stromal VEGF expression and microvessel density. The expression of NOS in the epithelial cells was strong, and showed no differences between the different groups of tumours.

Conclusions: Higher stromal expression of NOS in phyllodes tumours is associated with malignancy, suggesting a possible role in malignant progression, particularly metastasising potential.

  • e/i-NOS, endothelial/inducible nitric oxide synthase
  • NO, nitric oxide
  • VEGF, vascular endothelial growth factor
  • phyllodes
  • endothelial nitric oxide synthase
  • inducible nitric oxide synthase

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