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Expression of retinoid receptors in sebaceous cell carcinoma
Author(s) -
Chakravarti Nitin,
ElNaggar Adel K.,
Lotan Reuben,
Anderson James,
Diwan Abdul H.,
Saadati Hossein G.,
Diba Roxana,
Prieto Victor G.,
Esmaeli Bita
Publication year - 2006
Publication title -
journal of cutaneous pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.597
H-Index - 75
eISSN - 1600-0560
pISSN - 0303-6987
DOI - 10.1111/j.0303-6987.2006.00396.x
Subject(s) - retinoid , retinoid x receptor , biology , receptor , pathology , sebaceous gland , cancer research , endocrinology , nuclear receptor , retinoic acid , medicine , cell culture , transcription factor , biochemistry , gene , genetics
Purpose: The aim of this study is to investigate whether there are any abnormalities in the in vivo expression of retinoid acid receptors (RAR‐α, RAR‐β and RAR‐γ) and retinoid X receptors (RXR‐α, RXR‐β and RXR‐γ) in sebaceous cell carcinoma. Methods: Expression of retinoid receptors in paired specimens of cancerous tissues (n = 10) and adjacent normal tissues (n = 10) from 10 patients with sebaceous cell carcinoma was studied immunohistochemically by using anti‐retinoid receptor antibodies. Results: In eight of the 10 normal tissue samples, all six receptors were expressed. In the other two samples, all receptors were expressed except RAR‐γ (one sample) or RXR‐γ (two samples). Five tumours (50%) lacked RAR‐α; RAR‐α expression was lower in tumours than in normal tissues in eight of 10 cases. RAR‐β was expressed in the cytoplasm of nine of 10 tumours; RAR‐β expression was at least as high in tumours as in normal tissue in eight of 10 cases. Two tumours lacked RAR‐γ; three tumours had lower RAR‐γ expression than paired normal epithelium; four had the same RAR‐γ expression, and one had higher RAR‐γ expression. RXR‐α expression was strong in all normal tissues and tumour samples. Ten tumours lacked RXR‐β and all 10 tumours lacked RXR‐γ expression. Conclusions: Diminished RXR‐β and RXR‐γ expression might be related to the development of sebaceous cell carcinoma. Additional studies are required to establish whether the defects in RAR expression in sebaceous cell carcinoma might affect the potential response of this tumour to treatment with retinoids.