Journal article

Publication year: 2019

Journal: Cancers

Volume number: 11

Issue number: 12

eISSN: 2072-6694

Open access status: Gold

DOI Link: https://doi.org/10.3390/cancers11121826

Publisher: MDPI

Abstract: 
The epidermal growth factor receptor (EGFR) family contains four transmembrane tyrosine kinases (EGFR1/ErbB1, Her2/ErbB2, Her3/ErbB3 and Her4/ErbB4) and 13 secreted polypeptide ligands. EGFRs are overexpressed in many solid tumors, including breast, pancreas, head-and-neck, prostate, ovarian, renal, colon, and non-small-cell lung cancer. Such overexpression produces strong stimulation of downstream signaling pathways, which induce cell growth, cell differentiation, cell cycle progression, angiogenesis, cell motility and blocking of apoptosis.The high expression and/or functional activation of EGFRs correlates with the pathogenesis and progression of several cancers, which make them attractive targets for both diagnosis and therapy. Several approaches have been developed to target these receptors and/or the EGFR modulated effects in cancer cells. Most approaches include the development of anti-EGFRs antibodies and/or small-molecule EGFR inhibitors. This review presents the state-of-the-art and future prospects of targeting EGFRs to treat breast cancer.

Harvard Citation style: Maennling, A., Tur, M., Niebert, M., Klockenbring, T., Zeppernick, F., Gattenloehner, S., et al. (2019) Molecular Targeting Therapy against EGFR Family in Breast Cancer: Progress and Future Potentials, Cancers, 11(12), Article 1826. https://doi.org/10.3390/cancers11121826

APA Citation style: Maennling, A., Tur, M., Niebert, M., Klockenbring, T., Zeppernick, F., Gattenloehner, S., Meinhold-Heerlein, I., & Hussain, A. (2019). Molecular Targeting Therapy against EGFR Family in Breast Cancer: Progress and Future Potentials. Cancers. 11(12), Article 1826. https://doi.org/10.3390/cancers11121826