rss
J Clin Pathol 2004;57:168-171 doi:10.1136/jcp.2003.007260
  • Original article

The immunohistochemical localisation of somatostatin receptors 1, 2, 3, and 5 in acoustic neuromas

  1. N D Stafford1,
  2. L T Condon1,
  3. M J C Rogers1,
  4. L Helboe2,
  5. D A Crooks3,
  6. S L Atkin4
  1. 1Department of Otolaryngology-Head and Neck Surgery, Hull Royal Infirmary, Anlaby Road, Hull HU3 2JZ, UK
  2. 2Department of Neurobiology, H. Lundbeck A/S, Ottiliavej 7, DK-2500 Valby, Denmark
  3. 3Department of Neuropathology, Hull Royal Infirmary
  4. 4Department of Diabetes and Endocrinology, Michael White Diabetes Centre, Hull Royal Infirmary
  1. Correspondence to:
 Professor N D Stafford
 Postgraduate Medical Institute, Cohen Building, Room 267, The University of Hull, Cottingham Road, Hull HU6 7RX, UK; N.D.Staffordhull.ac.uk
  • Accepted 7 April 2003

Abstract

Aims: Acoustic neuroma is a benign tumour, which develops through an overproliferation of Schwann cells along the vestibular nerve. Somatostatin is a naturally occurring peptide, which exerts antiproliferative and antiangiogenic effects via five membrane bound receptor subtypes. The aim of this study was to determine whether somatostatin receptor subtypes (SSTRs) 1, 2, 3, and 5 are present in acoustic neuromas.

Methods: The expression of SSTRs 1, 2, 3, and 5 was studied in both the Schwann cells and blood vessels of eight acoustic neuroma specimens, by means of immunohistochemistry using novel rabbit polyclonal antibodies raised against human SSTR 1, 2, and 5 subtype specific peptides, and a commercial anti-SSTR3 antibody.

Results: SSTR2 was the most prevalent subtype in Schwann cells (seven of eight), with intermediate expression of SSTR3 (six of eight), and lower expression of SSTRs 1 and 5 (four of eight and five of eight, respectively). There was ubiquitous vascular expression of SSTR2, with no evidence of SSTR 1, 3, or 5 expression in blood vessels.

Conclusion: SSTRs 1, 2, 3, and 5 are differentially expressed in acoustic neuromas. Somatostatin analogues may have a therapeutic role in the management of this rare and challenging condition.

Footnotes

    Register for free content

    The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

    Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.