Primary cells from patients with adult T cell leukemia/lymphoma depend on HTLV-1 Tax expression for NF-κB activation and survival.
Rita HleihelHala SkaynehHugues de ThéOlivier HermineAli BazarbachiPublished in: Blood cancer journal (2023)
Adult T cell leukemia/lymphoma (ATL) is an aggressive malignancy secondary to chronic infection with human T cell leukemia virus type 1 (HTLV-1). The viral oncoprotein Tax initiates T cell transformation through activation of critical cellular pathways, including NF-κB. Unexpectedly, Tax protein is not detectable in most ATL cells, in contrast to the HTLV-1 HBZ protein which antagonizes Tax effects. Here, we demonstrate that primary ATL cells from patients with acute or chronic ATL express very low levels of Tax mRNA and protein. Critically, survival of these primary ATL cells is dependent on continued Tax expression. Mechanistically, Tax extinction results in reversal of NF-κB activation, P53/PML activation and apoptosis. Tax drives interleukin-10 (IL-10) expression and recombinant IL-10 rescues the survival of tax-depleted primary ATL cells. These results demonstrate the critical role of continued Tax and IL-10 expression for the survival of primary ATL cells, highlighting their relevance as therapeutic targets.
Keyphrases
- cell cycle arrest
- induced apoptosis
- poor prognosis
- binding protein
- signaling pathway
- pi k akt
- oxidative stress
- cell death
- acute myeloid leukemia
- endoplasmic reticulum stress
- bone marrow
- lps induced
- inflammatory response
- endothelial cells
- magnetic resonance
- sars cov
- diffuse large b cell lymphoma
- mouse model
- computed tomography
- toll like receptor
- long non coding rna