A Brief Overview of the Paradoxical Role of Glucocorticoids in Breast Cancer.
Ekaterina M ZhidkovaEvgeniya S LylovaAlena V SavinkovaSergey A MertsalovKirill I KirsanovGennady A BelitskyMarianna G YakubovskayaEkaterina A LesovayaPublished in: Breast cancer : basic and clinical research (2020)
Glucocorticoids (GCs) are stress hormones that play multiple roles in the regulation of cancer cell differentiation, apoptosis, and proliferation. Some types of cancers, such as hematological malignancies, can be effectively treated by GCs, whereas the responses of epithelial cancers to GC treatment vary, even within cancer subtypes. In particular, GCs are frequently used as supporting treatment of breast cancer (BC) to protect against chemotherapy side effects. In the therapy of nonaggressive luminal subtypes of BC, GCs can have auxiliary antitumor effects due to their cytotoxic actions on cancer cells. However, GCs can promote BC progression, colonization of distant metastatic sites, and metastasis. The effects of GCs on cell proliferation vary with BC subtype and its molecular profile and are realized via the activation of glucocorticoid receptor (GR), a well-known transcriptional factor involved in the regulation of the expression of multiple genes, cell-cell adhesion, and cell migration and polarity. This review focuses on the roles of GC signaling in the adhesion, migration, and metastasis of BC cells. We discuss the molecular mechanisms of GC actions that lead to BC metastasis and propose alternative pharmacological uses of GCs for BC treatment.
Keyphrases
- cell migration
- cell proliferation
- small cell lung cancer
- cell adhesion
- cell cycle arrest
- papillary thyroid
- squamous cell carcinoma
- poor prognosis
- stem cells
- induced apoptosis
- oxidative stress
- cystic fibrosis
- replacement therapy
- genome wide
- escherichia coli
- dna methylation
- single cell
- pseudomonas aeruginosa
- endoplasmic reticulum stress
- cell death
- cell cycle
- combination therapy
- childhood cancer
- long non coding rna
- gene expression
- bone marrow
- rectal cancer
- staphylococcus aureus
- single molecule
- chemotherapy induced
- bioinformatics analysis