Clinical use of selective estrogen receptor modulators and down regulators with the main focus on breast cancer

C K Baumann1, M Castiglione-Gertsch

  • 1Clinic and Policlinic for Medical Oncology, University Hospital, Bern, Switzerland. christa-baumann@bluewin.ch

Minerva Ginecologica
|November 28, 2009
PubMed

Insights

Selective estrogen receptor modulators (SERMs) and down regulators (SERDs) offer targeted estrogen receptor modulation for breast cancer treatment. Research explores their evolving role alongside aromatase inhibitors and genetic markers for personalized therapy.

Area of Science:

  • Endocrinology
  • Oncology
  • Pharmacology

Background:

  • Endocrine therapies have been a cornerstone of breast cancer treatment since the late 19th century.
  • Selective estrogen receptor modulators (SERMs) and selective estrogen down regulators (SERDs) represent key advancements in targeting estrogen receptor (ER) pathways.
  • Tamoxifen, a prominent SERM, has been widely used across various breast cancer settings, but its role is evolving.

Purpose of the Study:

  • To review the development and application of SERMs and SERDs in breast cancer treatment and prevention.
  • To discuss the current landscape of endocrine therapy, including the impact of aromatase inhibitors and emerging targeted therapies.
  • To explore the potential of genetic markers, such as CYP2D6 polymorphisms, in predicting treatment response.

Main Methods:

  • Literature review of SERMs and SERDs in breast cancer.
  • Analysis of clinical trial data comparing tamoxifen with aromatase inhibitors.
  • Discussion of emerging research on endocrine therapy sequencing and combination strategies.

Main Results:

  • Aromatase inhibitors demonstrate higher efficacy than tamoxifen in certain breast cancer contexts, with distinct toxicity profiles.
  • While several SERMs have been investigated, none have definitively surpassed tamoxifen, though safety profiles may differ.
  • SERDs are primarily used in advanced breast cancer, with further research needed for other settings.

Conclusions:

  • The optimal role of tamoxifen, other SERMs, and SERDs in breast cancer treatment is under re-evaluation due to advancements in endocrine therapy and targeted treatments.
  • Sequencing of endocrine therapies and combinations with novel targeted agents are critical research areas for hormone-sensitive breast cancer.
  • Genetic profiling, like CYP2D6 genotyping, may offer predictive markers for tamoxifen response, potentially redefining its future clinical application.

Related Concept Videos

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: Nuclear Receptors01:31

Transducer Mechanism: Nuclear Receptors

Nuclear receptors, or NRs, are unique transcription factors that regulate gene transcription and affect the cellular pathways involved in reproduction, development, or metabolism. Their ability to be stimulated by small lipophilic ligands and control vital cellular processes makes them ideal drug targets. Nearly 10-15% of currently prescribed drugs target these receptors.
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:
Receptor Downregulation in MVBs01:15

Receptor Downregulation in MVBs

Multivesicular bodies (MVBs) are mature endosomes that sort ubiquitinated proteins and then fuse with lysosomes to degrade the sorted proteins. Epidermal growth factor (EGF) and its receptor (EGFR) form a complex that can be internalized through endocytosis, sorted into an MVB, and later degraded.
The EGFR can initiate signaling pathways that  lead to cell proliferation, migration, and differentiation. Overexpression of EGFR  stimulates cells to proliferate. Excessive  EGFR activation may...
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...