作者: Julie A. Lofgren , Brian M. Fendly , Andrew Nuijens , Gail D. Lewis , Mark X. Sliwkowski
DOI:
关键词: Cell cycle 、 Biology 、 Internal medicine 、 ERBB3 、 Ovarian tumor 、 Neuregulin 、 Neuregulin 1 、 Cell division 、 Endocrinology 、 Cell growth 、 Epidermal growth factor 、 Cancer research
摘要: Alterations in the expression of epidermal growth factor (EGF) receptor ErbB family are frequently encountered a number human cancers. Two these receptors, ErbB3 and ErbB4, known to bind related proteins termed heregulins (HRGs) or neu differentiation factors. In biologically relevant systems, interaction HRG with ErbB4 results transactivation ErbB2. this report, we show that ErbB2 is critical component mediating responsiveness panel breast ovarian tumor cell lines. Because HRGs have been reported elicit diverse biological effects on cultured cells, including stimulation, inhibition, induction differentiation, systematically examined effect rHRG beta 1 proliferation. binding studies were performed lines expressing range levels The responses also compared EGF growth-inhibitory anti-ErbB2 antibody, 4D5. most cases, stimulation DNA synthesis correlated positive cycle progression enhancement colony formation soft agar. On each line tested, distinguishable from Our findings indicate induces proliferation addition, methods for measuring proliferation, as well experimental conditions, determining vitro.