TY - JOUR
T1 - Anti-HER2 antibody enhances the growth inhibitory effect of anti-oestrogen on breast cancer cells expressing both oestrogen receptors and HER2
AU - Kunisue, H.
AU - Kurebayashi, J.
AU - Otsuki, T.
AU - Tang, C. K.
AU - Kurosumi, M.
AU - Yamamoto, S.
AU - Tanaka, K.
AU - Doihara, H.
AU - Shimizu, N.
AU - Sonoo, H.
N1 - Funding Information:
This work is partly supported by grants from the Ministry of Education, Science, Sports and Culture of Japan (to J Kurebayashi), from the Ministry of Health of Japan (to H Sonoo) and by Research Grants (no. 10–113 to J Kurebayashi and no. 10–307 to H Sonoo) from Kawasaki Medical School.
PY - 2000
Y1 - 2000
N2 - Anti-oestrogen is effective for the treatment of oestrogen receptor (ER)-positive breast carcinomas, but most of these tumours become resistant to anti-oestrogen. It has been suggested that anti-oestrogen therapy may induce a HER2 signalling pathway in breast cancer cells and this may cause resistance to anti-oestrogen. Thus, it is conceivable that combined therapy with anti-oestrogen and anti-HER2 antibody might be more effective. In the present study, we investigated the effect of combined treatment with a humanized anti-HER2 monoclonal antibody, rhumAbHER2 (trastuzumab), and an anti-oestrogen, ICI 182,780, on the cell growth of three human breast cancer cell lines which respectively express different levels of ER and HER2. The combined treatment enhanced the growth inhibitory effect on ML-20 cells, which express a high level of ER and a moderate level of HER2, but showed no additive effect on either KPL-4 cells, which express no ER and a moderate level of HER2, or MDA-MB-231 cells, which express no ER and a low level of HER2. It is also suggested that both the antibody and anti-oestrogen induce a G1-S blockade and apoptosis. These findings indicate that combined treatment with anti-HER2 antibody and anti-oestrogen may be useful for the treatment of patients with breast cancer expressing both ER and HER2.
AB - Anti-oestrogen is effective for the treatment of oestrogen receptor (ER)-positive breast carcinomas, but most of these tumours become resistant to anti-oestrogen. It has been suggested that anti-oestrogen therapy may induce a HER2 signalling pathway in breast cancer cells and this may cause resistance to anti-oestrogen. Thus, it is conceivable that combined therapy with anti-oestrogen and anti-HER2 antibody might be more effective. In the present study, we investigated the effect of combined treatment with a humanized anti-HER2 monoclonal antibody, rhumAbHER2 (trastuzumab), and an anti-oestrogen, ICI 182,780, on the cell growth of three human breast cancer cell lines which respectively express different levels of ER and HER2. The combined treatment enhanced the growth inhibitory effect on ML-20 cells, which express a high level of ER and a moderate level of HER2, but showed no additive effect on either KPL-4 cells, which express no ER and a moderate level of HER2, or MDA-MB-231 cells, which express no ER and a low level of HER2. It is also suggested that both the antibody and anti-oestrogen induce a G1-S blockade and apoptosis. These findings indicate that combined treatment with anti-HER2 antibody and anti-oestrogen may be useful for the treatment of patients with breast cancer expressing both ER and HER2.
KW - Additive effect
KW - Anti-HER2 antibody
KW - Anti-oestrogen
KW - Apoptosis
KW - Breast cancer
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U2 - 10.1054/bjoc.1999.0875
DO - 10.1054/bjoc.1999.0875
M3 - Article
C2 - 10638965
AN - SCOPUS:0033986779
SN - 0007-0920
VL - 82
SP - 46
EP - 51
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 1
ER -