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Journal ArticleDOI

ERBB receptors and cancer: the complexity of targeted inhibitors.

TLDR
This work discusses the significance of these receptors as clinical targets, in particular the molecular mechanisms underlying response, and many ERBB inhibitors used in the clinic.
Abstract
ERBB receptor tyrosine kinases have important roles in human cancer. In particular, the expression or activation of epidermal growth factor receptor and ERBB2 are altered in many epithelial tumours, and clinical studies indicate that they have important roles in tumour aetiology and progression. Accordingly, these receptors have been intensely studied to understand their importance in cancer biology and as therapeutic targets, and many ERBB inhibitors are now used in the clinic. We will discuss the significance of these receptors as clinical targets, in particular the molecular mechanisms underlying response.

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PET and SPECT Imaging of Tumor Biology: New Approaches towards Oncology Drug Discovery and Development.

TL;DR: This review will focus on recent studies of PET and SPECT radioligands in oncology and their application in the investigation of tumor biology and the use of clinically-validated radiolIGands as imaging-based biomarkers in Oncology could significantly impact new cancer therapeutic development.
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Algorithms for Drug Sensitivity Prediction

TL;DR: A review of approaches that have been proposed to tackle the drug sensitivity prediction problem especially with respect to personalized cancer therapy is considered and modeling approaches that are based on genomic characterizations alone are discussed.
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Gene targeting of ErbB3 using a Cre-mediated unidirectional DNA inversion strategy.

TL;DR: To test the feasibility of unidirectional DNA inversion by in vivo recombination, a member of the ErbB family of tyrosine kinase receptors was targeted using this strategy and the extent to which this strategy results in effective gene knockout was established.
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Calcitriol and its analogues enhance the antiproliferative activity of gefitinib in breast cancer cells.

TL;DR: The combination of gefitinib with calcitriol or their synthetic analogs resulted in a greater antiproliferative effect than with either of the agents alone in EGFR and HER2 positive breast cancer cells.
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The Asn418-Linked N-Glycan of ErbB3 Plays a Crucial Role in Preventing Spontaneous Heterodimerization and Tumor Promotion

TL;DR: Findings suggest that the Asn(418)-linked N-glycan in ErbB3 plays an essential role in regulating receptor heterodimerization with ErbbB2 and might have an effect on transforming activity.
References
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Journal ArticleDOI

The hallmarks of cancer.

TL;DR: This work has been supported by the Department of the Army and the National Institutes of Health, and the author acknowledges the support and encouragement of the National Cancer Institute.
Journal ArticleDOI

Human breast cancer: correlation of relapse and survival with amplification of the HER-2/neu oncogene

TL;DR: Amplification of the HER-2/neu gene was a significant predictor of both overall survival and time to relapse in patients with breast cancer, and had greater prognostic value than most currently used prognostic factors in lymph node-positive disease.
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Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib

TL;DR: A subgroup of patients with non-small-cell lung cancer have specific mutations in the EGFR gene which correlate with clinical responsiveness to the tyrosine kinase inhibitor gefitinib, and these mutations lead to increased growth factor signaling and confer susceptibility to the inhibitor.
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Use of Chemotherapy plus a Monoclonal Antibody against HER2 for Metastatic Breast Cancer That Overexpresses HER2

TL;DR: The addition of trastuzumab to chemotherapy was associated with a longer time to disease progression, a higher rate of objective response, a longer duration of response, and a lower rate of death at 1 year.
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