We have previously reported, using the polymerase chain reaction (PCR), the
presence of a 660 bp sequence homologous to the env gene of MMTV in 38% of
the human breast cancers studied, but not in normal breasts nor in other t
umors or tissues. We have now investigated the presence of MMTV-like LTR se
quences in human breast cancer and normal breast tissue, Primers were selec
ted to amplify a 630 bp sequence homologous to MMTV, but not to the endogen
ous retrovirus HERV-K10. This sequence was detected in 41.5% of the breast
cancers and none of the normal breasts. A larger 1.2 kb LTR fragment was al
so amplified with high homology to MMTV. Finally, a 1.6 kb fragment contain
ing env and LTR sequences was amplified, cloned and sequenced from breast c
ancer DNA. The human LTRs were highly homologous to MMTV contain enhancer a
nd promoter elements, the glucocorticoid responsive element (GRE) and the s
uperantigen (Sag) sequences. Presence of functional sequences implies invol
vement in transcriptional regulation, whereas presence of an env-LTR sequen
ce indicates contiguity within the genome of a potential provirus. Their pr
esence in breast cancer DNA, but not in normal tissue, suggest an exogenous
origin.