Abstract

BackgroundAdult T-cell leukemia/lymphoma (ATLL) is a malignancy derived from T cells infected with human T-cell leukemia virus type 1 (HTLV-1), and it is known to be resistant to standard anticancer therapies. Indole-3-carbinol (I3C), a naturally occurring component of Brassica vegetables such as cabbage, broccoli and Brussels sprout, is a promising chemopreventive agent as it is reported to possess antimutagenic, antitumorigenic and antiestrogenic properties in experimental studies. The aim of this study was to determine the potential anti-ATLL effects of I3C both in vitro and in vivo.ResultsIn the in vitro study, I3C inhibited cell viability of HTLV-1-infected T-cell lines and ATLL cells in a dose-dependent manner. Importantly, I3C did not exert any inhibitory effect on uninfected T-cell lines and normal peripheral blood mononuclear cells. I3C prevented the G1/S transition by reducing the expression of cyclin D1, cyclin D2, Cdk4 and Cdk6, and induced apoptosis by reducing the expression of XIAP, survivin and Bcl-2, and by upregulating the expression of Bak. The induced apoptosis was associated with activation of caspase-3, -8 and -9, and poly(ADP-ribose) polymerase cleavage. I3C also suppressed IκBα phosphorylation and JunD expression, resulting in inactivation of NF-κB and AP-1. Inoculation of HTLV-1-infected T cells in mice with severe combined immunodeficiency resulted in tumor growth. The latter was inhibited by treatment with I3C (50 mg/kg/day orally), but not the vehicle control.ConclusionOur preclinical data suggest that I3C could be potentially a useful chemotherapeutic agent for patients with ATLL.

Highlights

  • Adult T-cell leukemia/lymphoma (ATLL) is a malignancy derived from T cells infected with human T-cell leukemia virus type 1 (HTLV-1), and it is known to be resistant to standard anticancer therapies

  • Adult T-cell leukemia/lymphoma (ATLL) is a fatal T-cell malignancy caused by infection of mature CD4+ T cells by human T-cell leukemia virus type 1 (HTLV-1) [1,2,3]

  • We investigated the effects of I3C on cell growth and apoptosis of HTLV-1-infected and uninfected T-cell lines and primary ATLL cells

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Summary

Introduction

Adult T-cell leukemia/lymphoma (ATLL) is a malignancy derived from T cells infected with human T-cell leukemia virus type 1 (HTLV-1), and it is known to be resistant to standard anticancer therapies. Adult T-cell leukemia/lymphoma (ATLL) is a fatal T-cell malignancy caused by infection of mature CD4+ T cells by human T-cell leukemia virus type 1 (HTLV-1) [1,2,3]. ATLL is clinically and hematologically subclassified into four subtypes: acute, lymphoma, chronic and smoldering. In the relatively indolent smoldering and chronic types, the median survival time is ≥ 2 years. There is no accepted curative therapy for ATLL and the condition often progresses to death with a median survival time of 13 months in aggressive ATLL [4]. The establishment of new therapeutic strategies for ATLL is deemed critical

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