Osteopontin Expression in Normal Skin and Non-melanoma Skin Tumors
Author(s) -
PiLing Chang,
Louie Harkins,
YuHua Hsieh,
Patricia H. Hicks,
Kraisorn Sappayatosok,
Somchai Yodsanga,
Somporn Swasdison,
Ann F. Chambers,
Craig A. Elmets,
Kang-Jey Ho
Publication year - 2007
Publication title -
journal of histochemistry and cytochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.971
H-Index - 124
eISSN - 1551-5044
pISSN - 0022-1554
DOI - 10.1369/jhc.7a7325.2007
Subject(s) - osteopontin , pathology , carcinogenesis , matricellular protein , actinic keratosis , skin cancer , human skin , basal cell carcinoma , immunohistochemistry , keratinocyte , cell , chemistry , cancer , cancer research , biology , medicine , extracellular matrix , basal cell , microbiology and biotechnology , immunology , in vitro , biochemistry , genetics
Osteopontin (OPN) is an adhesive, matricellular glycoprotein, whose expression is elevated in many types of cancer and has been shown to facilitate tumorigenesis in vivo. To understand the role of OPN in human skin cancer, this study is designed to determine whether OPN is expressed in premalignant [solar/actinic keratosis (AK)] and in malignant skin lesions such as squamous cell carcinomas (SCC) and basal cell carcinomas (BCC), as well as in normal skin exposed or not exposed to sunlight. Immunohistochemical analyses showed that OPN is expressed in SCC (20/20 cases) and in AK (16/16 cases), which are precursors to SCC, but is absent or minimally expressed in solid BCC (17 cases). However, positive staining for OPN was observed in those BCC that manifest differentiation toward epidermal appendages such as keratotic BCC. In sunlight-exposed normal skin, OPN is minimally expressed in the basal cell layer, but in contrast to those not exposed to sunlight, OPN is more prominent in the spinous cell layer with increasing intensity toward the granular cell layer. Additionally, OPN is expressed in the hair follicles, sebaceous glands, and sweat glands of normal skin. In conclusion, these data suggest that OPN is associated with keratinocyte differentiation and that it is expressed in AK and SCC, which have metastatic potential, but minimally expressed in solid BCC.
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