Receptor polymorphisms and diseases.

A Császár, T Abel

Journal: European journal of pharmacology 2001;414(1):9-22

PMID: 11230990

Full Text on Elsevier Science View on PubMed

Abstract

The aim of our review is to summarize common genetic variations of some receptors associated with clinical consequences, which were not outlined in the previous special issue of this journal. Because of the multiple pathomechanisms of diseases, a set of genetic variation can play a role in the development of pathological conditions. From the data available three articles would merit a greater interest. In systemic lupus erythematosus the associations related to some polymorphisms of Fc-, tumor necrosis factor (TNF) alpha- and interferon receptor may explore new autoimmunological and inflammatorical pathomechanisms. In the endocrinology, the androgen receptor repeat polymorphism will exert significant aspects in the development of prostate cancer. The pleoitropic responsibility of vitamin D3 receptor polymorphism in the pathogenesis of immunological disorders (primary biliary cirrhosis, inflammatory bowel disease, type 1 diabetes mellitus) and of malignancies (malignant melanoma, breast cancer) shed light on the importance of common nuclear receptors. Nevertheless, in the future studies a more consistent approach minimizing requirement bias in the selection of patients will approve our understanding the role of genetic influence on the pathogenesis of diseases.

Address: Department of Medicine and Geriatrics, Faculty of Health Sciences, Semmelweis University, Szabolcs u. 33-35, H-1135, Budapest, Hungary. [email protected]

DOI: 10.1016/s0014-2999(01)00755-5

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MeSH Terms: Antigens, CD, Arteriosclerosis, Diabetes Mellitus, Type 1, Humans, Inflammatory Bowel Diseases, Interferon-gamma, Liver Cirrhosis, Biliary, Lupus Erythematosus, Systemic, Male, Metabolic Diseases, Patient Selection, Phenotype, Polymorphism, Genetic, Prostatic Neoplasms, Receptors, Androgen, Receptors, Calcitriol, Receptors, Cell Surface, Receptors, Chemokine, Receptors, Estrogen, Receptors, Fc, Receptors, Interferon, Receptors, Tumor Necrosis Factor, Receptors, Tumor Necrosis Factor, Type II