[Targeting epidermal growth factor receptor in cancer of the breast]

Véronique Diéras1, Jean-Yves Pierga, Anne Vincent-Salomon

  • 1Département d'oncologie médicale, Institut Curie, 26, rue d'Ulm, 75005 Paris. veronique.dieras@curie.net

Bulletin Du Cancer
|February 7, 2004
PubMed

Insights

Targeting the epidermal growth factor receptor (EGFR) shows promise in treating breast cancer, potentially preventing hormone resistance and aiding chemoprevention. Further research into the erbB network is needed for optimal patient selection.

Area of Science:

  • Oncology
  • Molecular Biology
  • Pharmacology

Background:

  • The erbB receptor family, part of the receptor tyrosine kinase superfamily, is crucial in normal breast development and breast cancer progression.
  • Overexpression of erbB receptors is linked to poor prognosis, increased tumor invasiveness, and resistance to standard therapies like chemotherapy and hormonotherapy.

Purpose of the Study:

  • To explore the potential of targeting the epidermal growth factor receptor (EGFR) in breast cancer treatment.
  • To evaluate the efficacy of EGFR-targeting agents, particularly tyrosine kinase inhibitors, in various breast cancer contexts.

Main Methods:

  • Review of experimental data on EGFR targeting strategies, including tyrosine kinase inhibitors and monoclonal antibodies.
  • Analysis of studies investigating the combination of EGFR inhibitors with hormonotherapy, chemotherapy, and trastuzumab.
  • Examination of in situ carcinoma studies regarding chemoprevention roles.

Main Results:

  • Tyrosine kinase inhibitors show activity as monotherapy and in combination with other breast cancer treatments.
  • EGFR inhibitors, such as Iressa, may prevent or overcome hormone resistance when combined with hormonotherapy.
  • Evidence suggests tyrosine kinase inhibitors could play a role in breast cancer chemoprevention.

Conclusions:

  • Targeting EGFR is a viable strategy for a broad range of breast tumors, from early to advanced stages, and across hormone receptor statuses.
  • The complexity of the erbB network necessitates targeting multiple molecular sites and characterizing tumor profiles for effective patient selection.

Related Concept Videos

Mitogens and the Cell Cycle02:38

Mitogens and the Cell Cycle

Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against specific...
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against specific...
Transducer Mechanism: Enzyme-Linked Receptors01:27

Transducer Mechanism: Enzyme-Linked Receptors

Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. Drugs can bind to the extracellular ligand-binding domain or directly affect their enzymatic domain and alter their activity.
Major types that are helpful drug targets include:
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase01:11

Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase

Genetic polymorphisms in drug targets have emerged as critical determinants of interindividual variability in drug response and toxicity. Pharmacogenomic investigations increasingly focus on identifying these variations to personalize and optimize therapeutic interventions. A drug target may be a receptor, enzyme, or signaling protein involved in pharmacologic responses or disease-related pathways. While early pharmacogenetic studies focused primarily on drug metabolism, current research...