Vorinostat (SAHA) and Breast Cancer: An Overview.
Anna WawruszakLidia BorkiewiczEstera OkonWirginia Kukuła-KochSyeda AfshanMarta HalasaPublished in: Cancers (2021)
Vorinostat (SAHA), an inhibitor of class I and II of histone deacetylases, is the first histone deacetylase inhibitor (HDI) approved for the treatment of cutaneous T-cell lymphoma in 2006. HDIs are promising anticancer agents that inhibit the proliferation of many types of cancer cells including breast carcinoma (BC). BC is a heterogeneous disease with variable biological behavior, morphological features, and response to therapy. Although significant progress in the treatment of BC has been made, high toxicity to normal cells, serious side effects, and the occurrence of multi-drug resistance limit the effective therapy of BC patients. Therefore, new active agents which improve the effectiveness of currently used regimens are highly needed. This manuscript analyzes preclinical and clinical trials data of SAHA, applied individually or in combination with other anticancer agents, considering different histological subtypes of BC.
Keyphrases
- histone deacetylase
- clinical trial
- end stage renal disease
- randomized controlled trial
- newly diagnosed
- systematic review
- induced apoptosis
- dna methylation
- chronic kidney disease
- combination therapy
- big data
- prognostic factors
- machine learning
- cell therapy
- peritoneal dialysis
- mesenchymal stem cells
- young adults
- patient reported
- phase ii
- data analysis
- phase iii