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KML001 Cytotoxic Activity Is Associated with Its Binding to Telomeric Sequences and Telomere Erosion in Prostate Cancer Cells

Authors' Affiliations: Departments of ¹ Pharmacology and Experimental Therapeutics and ² Pathology, Cytogenetics Laboratory, University of Maryland; ³ Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, Maryland; ⁴ Institute of Anatomy and Cell Biology, University of Freiburg, Freiburg, Germany; and ⁵ Hendriks Pharmaceutical Consulting, Purmerend, The Netherlands

Requests for reprints: Angelika M. Burger, Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Bressler Research Building, Room 9-039, 655 West Baltimore Street, Baltimore, MD 21201. Phone: 410-328-3914; Fax: 410-328-6559; E-mail: aburger{at}som.umaryland.edu.

Purpose: KML001 (sodium metaarsenite) is an orally bioavailable arsenic compound that has entered phase I/II clinical trials in prostate cancer. In this study, we elucidated the mode of action of KML001 and investigated its effects on telomerase and telomeres.

Experimental Design: We compared telomere length to KML001 cytotoxic activity in a panel of human solid tumor cell lines. Duration of exposure and concentrations of KML001 that affect telomerase and telomeres were evaluated in relation to established mechanisms of arsenite action such as reactive oxygen species–related DNA damage induction. Binding of KML001 to telomeres was assessed by matrix-assisted laser desorption/ionization mass spectrometry.

Results: We established a significant inverse correlation (r² = 0.9) between telomere length and cytotoxicity. KML001 exhibited activity in tumor cells with short telomeres at concentrations that can be achieved in serum of patients. We found that telomerase is not directly inhibited by KML001. Instead, KML001 specifically binds to telomeric sequences at a ratio of one molecule per three TTAGGG repeats leading to translocation of the telomerase catalytic subunit into the cytoplasm. In prostate cancer cells with short telomeres, KML001 caused telomere-associated DNA damage signaling as shown by -H2AX induction and chromatin immunoprecipitation assays as well as a rapid telomere erosion shown by metaphase fluorescence in situ hybridization. These effects were not seen in a lung cancer cell line with long telomeres. Importantly, arsenification of telomeres preceded DNA lesions caused by reactive oxygen species production.

Conclusions: Sodium metaarsenite is a telomere targeting agent and should be explored for the treatment of tumors with short telomeres.