Expression of gastrin‐releasing peptide receptor in patients with cutaneous malignant melanoma. (12th April 2013)
- Record Type:
- Journal Article
- Title:
- Expression of gastrin‐releasing peptide receptor in patients with cutaneous malignant melanoma. (12th April 2013)
- Main Title:
- Expression of gastrin‐releasing peptide receptor in patients with cutaneous malignant melanoma
- Authors:
- Marrone, B. F.
Meurer, L.
Moretto, A.
Kleina, W.
Schwartsmann, G. - Abstract:
- <abstract abstract-type="main" xml:lang="en" id="ced12058-abs-0001"> <title>Summary</title> <sec id="ced12058-sec-0001" sec-type="section"> <title>Background</title> <p>Gastrin‐releasing peptide (GRP) is a neuroendocrine peptide shown to possess growth‐stimulatory effects in many types of human cancers. High levels of GRP receptors have been found in various types of human cancers, and preclinical studies exploring the therapeutic use of GRP receptor (GRPR) antagonists have been reported, with promising results. Data on GRPR expression in human malignant melanoma (MM) are scanty.</p> </sec> <sec id="ced12058-sec-0002" sec-type="section"> <title>Aim</title> <p>To determine GRPR expression in biopsy material obtained from patients diagnosed with cutaneous MM.</p> </sec> <sec id="ced12058-sec-0003" sec-type="section"> <title>Methods</title> <p>Immunohistochemistry was performed on formalin–fixed, paraffin wax‐embedded tissue samples obtained from 51 patients with cutaneous MM. The relationship between GRPR expression and the clinicopathological features was analysed using the Fisher exact test.</p> </sec> <sec id="ced12058-sec-0004" sec-type="section"> <title>Results</title> <p>GRPR immunoexpression was found in 42/51 cutaneous melanoma samples (82.4%). It was strongly expressed in 30 cases (58.9%). There was no significant difference in the levels of GRPR expression between primary or metastatic lesions. We correlated the GRPR expression score with pathological features<abstract abstract-type="main" xml:lang="en" id="ced12058-abs-0001"> <title>Summary</title> <sec id="ced12058-sec-0001" sec-type="section"> <title>Background</title> <p>Gastrin‐releasing peptide (GRP) is a neuroendocrine peptide shown to possess growth‐stimulatory effects in many types of human cancers. High levels of GRP receptors have been found in various types of human cancers, and preclinical studies exploring the therapeutic use of GRP receptor (GRPR) antagonists have been reported, with promising results. Data on GRPR expression in human malignant melanoma (MM) are scanty.</p> </sec> <sec id="ced12058-sec-0002" sec-type="section"> <title>Aim</title> <p>To determine GRPR expression in biopsy material obtained from patients diagnosed with cutaneous MM.</p> </sec> <sec id="ced12058-sec-0003" sec-type="section"> <title>Methods</title> <p>Immunohistochemistry was performed on formalin–fixed, paraffin wax‐embedded tissue samples obtained from 51 patients with cutaneous MM. The relationship between GRPR expression and the clinicopathological features was analysed using the Fisher exact test.</p> </sec> <sec id="ced12058-sec-0004" sec-type="section"> <title>Results</title> <p>GRPR immunoexpression was found in 42/51 cutaneous melanoma samples (82.4%). It was strongly expressed in 30 cases (58.9%). There was no significant difference in the levels of GRPR expression between primary or metastatic lesions. We correlated the GRPR expression score with pathological features associated with prognosis in cutaneous MM. There was no significant difference in GRPR expression in relation to Clark level (CL;<italic> P </italic>= 0.35) or Breslow Index (BI;<italic> P </italic>= 0.17).</p> </sec> <sec id="ced12058-sec-0005" sec-type="section"> <title>Conclusions</title> <p>GRPR expression levels were high in tissue specimens of MM (82.4%), but did not correlate with pathological features related to prognosis, such as CL or BI. Further studies, preferably in a larger patient population, are warranted.</p> </sec> </abstract> … (more)
- Is Part Of:
- Clinical and experimental dermatology. Volume 38:Number 7(2013)
- Journal:
- Clinical and experimental dermatology
- Issue:
- Volume 38:Number 7(2013)
- Issue Display:
- Volume 38, Issue 7 (2013)
- Year:
- 2013
- Volume:
- 38
- Issue:
- 7
- Issue Sort Value:
- 2013-0038-0007-0000
- Page Start:
- 707
- Page End:
- 712
- Publication Date:
- 2013-04-12
- Subjects:
- Skin -- Diseases -- Periodicals
616.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2230 ↗
https://academic.oup.com/ced/issue ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/ced.12058 ↗
- Languages:
- English
- ISSNs:
- 0307-6938
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.250000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3347.xml