Ductal carcinoma in situ (DCIS) of the breast is commonly described as
a premalignant lesion, Using PCR to amplify DNA from areas of tumour
cells which have been microdissected from fixed material, we have stud
ied the involvement of chromosome 1 in 19 cases of DCIS, A series of m
icrosatellite repeat polymorphisms has been used to define regions of
allelic imbalance and this has confirmed the involvement in DCIS of si
x of the regions previously implicated in studies of invasive breast t
umours. This suggests that these regions may harbour tumour suppressor
genes, the inactivation of which is important for the early stages of
breast tumour development. Analysis of separate ducts from within the
same tumour has revealed-that the same genetic alterations are not ne
cessarily present throughout the lesion. In addition we have found tha
t in three cases where frank invasive carcinoma is also present, simil
ar alterations can be detected in the in situ and invasive component.