Targeting The Il-4/Il-13 Signaling Pathway Sensitizes Hodgkin Lymphoma Cells To Chemotherapeutic Drugs
INTERNATIONAL JOURNAL OF CANCER(2013)
Abstract
Hodgkin/Reed-Sternberg lymphoma (HL) is a clonal B-cell-related malignancy. Although many patients with HL can be cured by the current regimen of high-dose multi-agent chemotherapy, the treatment causes high risks of later pathologies including secondary malignancies. This fact highlights the demand to develop rational treatment for HL. Survival and growth of HL cells are largely dependent on their microenvironment. In this study, using the HL cell lines L1236 and KM-H2 as model systems, we investigated the role of IL-4/IL-13 signaling in regulation of drug sensitivity and resistance in HL. We show that specific blocking of IL-4 and IL-13-mediated STAT6 activation by either an IL-4-binding fusion protein APG598 or an IL-4R antagonist APG201 (R121D/Y124D) renders HL cells more prone to apoptotic killing by chemotherapeutic drugs such as Mitomycin C, 5-Fluorouracil, Etopside, Doxorubicin and Paclitaxel. This effect is due to inhibition of STAT6-mediated elevation of expression of the anti-apoptotic Bcl-2 family protein Bcl-xL. Employing ChIP analysis in combination with APG201 or STAT6-specific siRNA we identified a defined STAT6-binding site in the Bcl-xL promoter region from -1967 to -1957 of the transcription start site. Our data demonstrate that the IL-4/IL-13-STAT6-Bcl-xL axis may be an important target for HL treatment. This study also suggests that combination of classical chemotherapeutic drugs with the IL-4/IL-13 antagonists may enhance efficacy and reduce risks of toxicity from high dose of drugs in HL treatment.What's new? Hodgkin lymphoma (HL) is one of few cancers that can be cured, but the incidence of deadly secondary cancers and other side effects that emerge decades later as a result of HL chemotherapy indicates a need for safer treatment strategies. One such strategy, described in this report, may entail sensitization of HL cells to traditional chemotherapeutic drugs using IL-4 inhibitors. IL-4 signaling was found to induce activation of STAT6, leading to upregulation of the anti-apoptotic protein Bcl-xL in HL cells. The pathway was effectively disrupted by the IL-4 antagonists APG598 and APG201.
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Key words
cytokine, IL-4, IL-13, STAT6, Bcl-xL, Hodgkin lymphoma, apoptosis
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