| Literature DB >> 33466695 |
Marina Gerousi1,2, Fotis Psomopoulos1,3, Konstantia Kotta1, Maria Tsagiopoulou1, Niki Stavroyianni4, Achilles Anagnostopoulos4, Athanasios Anastasiadis5, Maria Gkanidou5, Ioannis Kotsianidis2, Stavroula Ntoufa1, Kostas Stamatopoulos1,3.
Abstract
It has been proposed that vitamin D may play a role in prevention and treatment of cancer while epidemiological studies have linked vitamin D insufficiency to adverse disease outcomes in various B cell malignancies, including chronic lymphocytic leukemia (CLL). In this study, we sought to obtain deeper biological insight into the role of vitamin D and its receptor (VDR) in the pathophysiology of CLL. To this end, we performed expression analysis of the vitamin D pathway molecules; complemented by RNA-Sequencing analysis in primary CLL cells that were treated in vitro with calcitriol, the biologically active form of vitamin D. In addition, we examined calcitriol effects ex vivo in CLL cells cultured in the presence of microenvironmental signals, namely anti-IgM/CD40L, or co-cultured with the supportive HS-5 cells; and, CLL cells from patients under ibrutinib treatment. Our study reports that the calcitriol/VDR system is functional in CLL regulating signaling pathways critical for cell survival and proliferation, including the TLR and PI3K/AKT pathways. Moreover, calcitriol action is likely independent of the microenvironmental signals in CLL, since it was not significantly affected when combined with anti-IgM/CD40L or in the context of the co-culture system. This finding was also supported by our finding of preserved calcitriol signaling capacity in CLL patients under ibrutinib treatment. Overall, our results indicate a relevant biological role for vitamin D in CLL pathophysiology and allude to the potential clinical utility of vitamin D supplementation in patients with CLL.Entities:
Keywords: RNA-sequencing; calcitriol; chronic lymphocytic leukemia; microenvironment; vitamin D receptor
Year: 2021 PMID: 33466695 PMCID: PMC7828837 DOI: 10.3390/cancers13020285
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639