Changes in [18F]Fluoro-2-deoxy-d-glucose incorporation induced by doxorubicin and anti-HER antibodies by breast cancer cells modulated by co-treatment with metformin and its effects on intracellular signalling
Author(s) -
Alasdair C. Cooper,
Ian N. Fleming,
Su Phyu,
Timothy Smith
Publication year - 2015
Publication title -
journal of cancer research and clinical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.338
H-Index - 94
eISSN - 1432-1335
pISSN - 0171-5216
DOI - 10.1007/s00432-015-1909-2
Subject(s) - metformin , skbr3 , breast cancer , ampk , doxorubicin , pharmacology , medicine , mapk/erk pathway , trastuzumab , cancer , mcf 7 , cancer cell , cancer research , endocrinology , chemistry , chemotherapy , phosphorylation , protein kinase a , biochemistry , insulin , human breast
Metformin, currently undergoing clinical trials as an adjuvant for the treatment of breast cancer, modulates the activity of key intracellular signalling molecules which affect 2-[(18)F]Fluoro-2-deoxy-D-glucose ([(18)F]FDG) incorporation. Here, we investigate the effect of drugs used in the treatment of breast cancer combined with metformin on [(18)F]FDG incorporation in HER2- or HER1-overexpressing breast cancer cells to determine whether or not metformin may obscure changes in [(18)F]FDG incorporation induced by clinically utilised anticancer drugs in the treatment of breast cancer.
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