Glutathione S-transferases mu (GSTM) are dimeric cytosolic isoenzymes.
They catalyze glutathione conjugation upon a large variety of electro
philes as carcinogens, trans-stilbene peroxide or benzo(a)pyrene. The
gene GSTM1 is localized on chromosome 1p13, it has drawn attention bec
ause it is absent approximately in 50% of the white population. GSTM1
null genotype seems linked with susceptibility to cancers as lung, col
on and bladder cancers. We have studied GSTM1 genotype from 373 primar
y breast tumours. The GSTM1 null genotype was found in 50% of the case
s (185/373). The incidence study of GSTM1 copy number on clinical and
biological variables displayed a significant difference (p < 0.01) of
the GSTM1 genotype, showed by the tumour, according to the patient age
at diagnosis. The patients younger than 55 years had a percentage mor
e important of primary tumours (65%) with a copy number of GSTM1 gene,
inferior or equal at one, compared to the patients older than 55 year
s (52%). The tumours, whose cathepsin D level was high, presented few
copies of GSTM1 gene (p < 0.03). There was no other relationship, part
icularly, with tumour size, node status, histological type, hormonal r
eceptors, pS2 cytosolic level GSTM1 gene seems protect the mammary gla
nd from cancerogenesis with its detoxification role. This result had n
ot, pointed out in breast cancer, yet.