4.1 Article

Proliferation, apoptosis, and survivin expression in a spectrum of melanocytic nevi

Journal

JOURNAL OF CUTANEOUS PATHOLOGY
Volume 32, Issue 1, Pages 45-49

Publisher

WILEY
DOI: 10.1111/j.0303-6987.2005.00242.x

Keywords

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Funding

  1. NATIONAL CENTER FOR RESEARCH RESOURCES [K23RR017525] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES [K08AR048618, R01AR050102] Funding Source: NIH RePORTER
  3. NCRR NIH HHS [K23RR17525, K23 RR017525] Funding Source: Medline
  4. NIAMS NIH HHS [KO8AR48618, R01 AR050102, R01 AR050102-02, K08 AR048618] Funding Source: Medline

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Background: Apoptosis is important for maintenance of tissue homeostasis and often dysregulated in cutaneous neoplasms. The apoptosis inhibitor survivin is expressed in melanoma and non-melanoma skin cancers and benign keratinocytic lesions. Its expression has not been studied in melanocytic nevi. Objective: We determined the expression pattern of survivin in benign melanocytic nevi in comparison to markers of proliferation and apoptosis. Methods: Six cases of each of the following melanocytic nevi were retrieved from a dermatopathology archive: compound dysplastic nevus, intradermal nevus, compound nevus, neurotized intradermal nevus, and Spitz nevus. Survivin expression was evaluated by in situ hybridization. Apoptotic and proliferation indices were calculated by counting immunoreactive cells in terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick end labeling and proliferating cell nuclear antigen immunostained sections, respectively. Results: All nevi, regardless of histologic type, expressed survivin. Compound melanocytic lesions expressed survivin in both epidermal and dermal compartments. The apoptotic rate was low for dysplastic, compound, and Spitz nevi, and apoptotic cells were not identified in any neurotized nevus. The proliferative index was highest for Spitz nevi, while all other nevi demonstrated rare positive cells. Conclusions: Survivin is consistently expressed in benign melanocytic lesions, while apoptotic cells are rarely identified, suggesting the dysregulation of apoptotic pathways with the accumulation of cells in these neoplasms.

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