Navitoclax Most Promising BH3 Mimetic for Combination Therapy in Hodgkin Lymphoma.
Myra LangendonkNienke A M SmitWouter PlattelArjan DiepstraTom van MeertenLidia VisserPublished in: International journal of molecular sciences (2022)
The treatment of young patients with Hodgkin lymphoma (HL) is often successful but a significant proportion of patients suffers from late toxicity. In the current era there are new opportunities for less toxic and more targeted treatment options. In this respect, the anti-apoptotic pathway is an attractive target since Hodgkin tumor cells abundantly express components of this pathway. We measured the effect of BH3 mimetics that interfere with anti-apoptotic proteins in cell lines, also in combination with the standard of care chemotherapeutic doxorubicin and the recently discovered preclinically active tamoxifen. Several anti-apoptotic BCL-2 family proteins were expressed in each case ( n = 84) and in HL cell lines ( n = 5). Cell lines were checked for sensitivity to BH3 mimetics by BH3 profiling and metabolic assays and monotherapy was only partially successful. Doxorubicin was synergistic with a BCL-XL inhibitor and BCL2/XL/W inhibitor navitoclax. Tamoxifen that targets the estrogen receptor β present in the mitochondria of the cell lines, could induce cell death, and was synergistic with several BH3 mimetics including/as well as navitoclax. In conclusion, targeting the anti-apoptotic pathway by the triple inhibitor navitoclax in combination with doxorubicin or tamoxifen is a promising treatment strategy in HL.
Keyphrases
- cell death
- hodgkin lymphoma
- estrogen receptor
- combination therapy
- cancer therapy
- drug delivery
- cell cycle arrest
- breast cancer cells
- end stage renal disease
- anti inflammatory
- healthcare
- newly diagnosed
- palliative care
- chronic kidney disease
- randomized controlled trial
- positive breast cancer
- oxidative stress
- cell proliferation
- clinical trial
- patient reported outcomes
- middle aged
- pain management