Differential Response of Mycosis Fungoides Cells to Vorinostat.
Zachary A BordeauxSriya V ReddyKevin LeeWeiying LuJustin ChoiMeghan N MillerCallie RobertsAnthony PollizziShawn G KwatraMadan M KwatraPublished in: International journal of molecular sciences (2023)
Mycosis fungoides (MF) is the most common form of cutaneous T-cell lymphoma (CTCL) and is characterized by epidermotrophism of malignant CD4+ T-lymphocytes. When MF advances to a recurrent stage, patients require treatment with systemic therapies such as vorinostat, a histone deacetylase inhibitor. While vorinostat has been shown to exhibit anti-tumor activity in MF, its exact molecular mechanism has yet to be fully discerned. In the present study, we examined the transcriptomic and proteomic profiles of vorinostat treatment in two MF cell lines, Myla 2059 and HH. We find that vorinostat downregulates CTLA-4, CXCR4, and CCR7 in both cell lines, but its effect on several key pathways differs between the two MF cell lines. For example, vorinostat upregulates CCL5, CCR5, and CXCL10 expression in Myla cells but downregulates CCL5 and CXCL10 expression in HH cells. Furthermore, vorinostat upregulates IFN-γ and IL-23 signaling and downregulates IL-6, IL-7, and IL-15 signaling in Myla cells but does not affect these pathways in HH cells. Although Myla and HH represent established MF cell lines, their distinct tumor origin from separate patients demonstrates that inherent phenotypic variations within the disease persist, underscoring the importance of using a variety of MF cells in the preclinical development of MF therapeutics.
Keyphrases
- induced apoptosis
- histone deacetylase
- cell cycle arrest
- dendritic cells
- endoplasmic reticulum stress
- poor prognosis
- newly diagnosed
- ejection fraction
- signaling pathway
- end stage renal disease
- cell death
- bone marrow
- cell proliferation
- prognostic factors
- single cell
- combination therapy
- peritoneal dialysis
- cell therapy
- drug induced
- molecular dynamics