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B Griffiths

Publications and source records attributed to B Griffiths.

38 records · Page 3Linked to original sources

Expression of the hypervariable PUM locus in normal and malignant lung: the tumor-associated epitopes are present but masked in normal tissue.

A single highly polymorphic gene locus PUM codes for a family of mucin-type glycoproteins present in human urine. These glycoproteins can be detected after electrophoresis using a group of monoclonal antibodies which show marked tumour specificity on immunohistology and include the HMFG and Ca antibodies (Swallow et al., 1986, 1987). Here we show by electrophoretic analysis of lung specimens and urine samples from nine individuals, that the PUM locus is expressed both in malignant and in normal lung. In contrast immunohistology of frozen sections of normal lung showed very little staining using the same antibodies, occasional reactive type 2 pneumocytes alone staining, whilst the carcinoma material showed strong staining in each case. However, after formalin fixation much more staining was observed in normal lung, all type 1 and 2 pneumocytes being stained. These observations suggest a difference in accessibility of the epitopes in normal and malignant lung, rather than a difference in expression of the PUM gene.

Antigens, Neoplasm

The breast tumour-associated epithelial mucins and the peanut lectin binding urinary mucins are coded by a single highly polymorphic gene locus 'PUM'.

A family of mucin-type glycoproteins, present in human urine, is coded by a single highly polymorphic gene locus PUM. We have previously shown that these glycoproteins carry epitopes recognized by a series of monoclonal antibodies, many of which were raised to the human milk-fat globule membrane, and which bind to a wide variety of carcinomas and certain normal epithelia. Here we show that in the normal human mammary gland, and in breast cancers the epitopes are present on the same family of molecules as that found in urine. Thus the genetically determined variation at the PUM locus accounts for much of the electrophoretic heterogeneity of the mucin-type glycoproteins present in breast cancer and serum from breast cancer patients that has been reported previously. Knowledge of this normal inherited polymorphism is essential to the interpretation of possible changes to these molecules in malignancy.

Antigens, Neoplasm