| Literature DB >> 35737241 |
Louisa L Wiede1, Sheila Drover2.
Abstract
Western blotting is an excellent technique to investigate aberrations and/or therapy-induced changes in signaling proteins in cancer. Using an in vitro system, we prepared whole cell lysates from HER2-overexpressing breast cancer cell lines, treated or not with the tyrosine kinase inhibitor, lapatinib, in the presence and absence of IFN-γ. Here we describe the protocol whereby proteins in the lysates were separated by SDS-PAGE, electrophoretically transferred to nitrocellulose membranes followed by an enzyme-linked immunoassay and chemiluminescence to reveal the relevant phosphorylated and dephosphorylated proteins. Herein, Western blot analysis confirmed lapatinib dephosphorylated HER2 and downstream signaling proteins and IFN-γ induced phosphorylation of STAT1.Entities:
Keywords: Breast cancer cells; Enzyme-linked immunoassay; Human epidermal growth factor receptor 2 (HER2); Lapatinib; Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE); Western blotting
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Year: 2022 PMID: 35737241 DOI: 10.1007/978-1-0716-2376-3_14
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745