Mitoxantrone in combination with an inhibitor of DNA-dependent protein kinase: a potential therapy for high risk B-cell chronic lymphocytic leukaemia
Sarah L. Elliott
The Newcastle Cancer Centre at the Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne
Search for more papers by this authorClark Crawford
The Newcastle Cancer Centre at the Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne
Search for more papers by this authorEvan Mulligan
The Newcastle Cancer Centre at the Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne
Search for more papers by this authorTryfonia Mainou-Fowler
The Newcastle Cancer Centre at the Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne
Search for more papers by this authorClare Bedwell
Northern Genetics Service, Newcastle upon Tyne NHS Hospitals Foundation Trust, Newcastle upon Tyne, UK
Search for more papers by this authorBarbara W. Durkacz
The Newcastle Cancer Centre at the Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne
Search for more papers by this authorElaine Willmore
The Newcastle Cancer Centre at the Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne
Search for more papers by this authorSarah L. Elliott
The Newcastle Cancer Centre at the Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne
Search for more papers by this authorClark Crawford
The Newcastle Cancer Centre at the Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne
Search for more papers by this authorEvan Mulligan
The Newcastle Cancer Centre at the Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne
Search for more papers by this authorTryfonia Mainou-Fowler
The Newcastle Cancer Centre at the Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne
Search for more papers by this authorClare Bedwell
Northern Genetics Service, Newcastle upon Tyne NHS Hospitals Foundation Trust, Newcastle upon Tyne, UK
Search for more papers by this authorBarbara W. Durkacz
The Newcastle Cancer Centre at the Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne
Search for more papers by this authorElaine Willmore
The Newcastle Cancer Centre at the Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne
Search for more papers by this authorSummary
Defects in the DNA damage response pathway [e.g. del(17p)] are associated with drug-resistant B-cell chronic lymphocytic leukaemia (CLL). We previously demonstrated that over-expression of DNA-dependent protein kinase (DNA-PK) correlates with chemo-resistance and that inhibition of DNA-PK sensitizes CLL cells to chemotherapeutics. Here, we investigated expression of DNA-PK and other proteins that impact on drug resistance, and evaluated the effects of a DNA-PK inhibitor (NU7441) on mitoxantrone-induced cytotoxicity in CLL cells. NU7441 sensitized cells from 42/49 CLL samples to mitoxantrone, with sensitization ranging from 2- to 200-fold Co-culture of CLL cells in conditioned stromal medium increased chemoresistance but did not reduce sensitization by NU7441. Mitoxantrone treatment induced γH2AX foci and NU7441 increased their longevity (24 h). NU7441 prevented mitoxantrone-induced autophosphorylation of the DNA-PK catalytic subunit (DNA-PKcs) at Ser 2056, confirming that DNA-PK participates in repair of mitoxantrone-induced DNA damage. del(17p) cases were more resistant to mitoxantrone than del(13q) cases, but were resensitized (7–16 fold) by co-incubation with NU7441. Expression of DNA-PKcs, Ku80, P-glycoprotein and topoisomerase IIβ were significantly higher in del(17p) cases. PRKDC mRNA levels correlated with DNA-PKcs protein expression, which predicted shorter survival. These data confirm the potential of DNA-PK as a therapeutic target in poor prognosis CLL.
References
- Adachi, N., Iiizumi, S., So, S. & Koyama, H. (2004) Genetic evidence for involvement of two distinct nonhomologous end-joining pathways in repair of topoisomerase II-mediated DNA damage. Biochemical and Biophysical Research Communications, 318, 856–861.
- Amrein, L., Loignon, M., Goulet, A.C., Dunn, M., Jean-Claude, B., Aloyz, R. & Panasci, L. (2007) Chlorambucil cytotoxicity in malignant B lymphocytes is synergistically increased by 2-(morpholin-4-yl)-benzo[h]chomen-4-one (NU7026)-mediated inhibition of DNA double-strand break repair via inhibition of DNA-dependent protein kinase. Journal of Pharmacology and Experimental Therapeutics, 321, 848–855.
- Austen, B., Powell, J.E., Alvi, A., Edwards, I., Hooper, L., Starczynski, J., Taylor, A.M., Fegan, C., Moss, P. & Stankovic, T. (2005) Mutations in the ATM gene lead to impaired overall and treatment-free survival that is independent of IGVH mutation status in patients with B-CLL. Blood, 106, 3175–3182.
- Beck, J., Niethammer, D. & Gekeler, V. (1994) High mdr1- and mrp-, but low topoisomerase II alpha-gene expression in B-cell chronic lymphocytic leukaemias. Cancer Letters, 86, 135–142.
- Beck, J., Niethammer, D. & Gekeler, V. (1996) Expression of MDR1, MRP, topoisomerase IIalpha/beta, and cyclin A gene expression in acute and chronic leukemias. Leukemia, 10(Suppl 3), S39–S45.
- Bellosillo, B., Colomer, D., Pons, G. & Gil, J. (1998) Mitoxantrone, a topoisomerase II inhibitor, induces apoptosis of B- chronic lymphocytic leukaemia cells. British Journal of Haematology, 100, 142–146.
- Bosch, F., Ferrer, A., Villamor, N., González, M., Briones, J., González-Barca, E., Abella, E., Gardella, S., Escoda, L., Pérez-Ceballos, E., Asensi, A., Sayas, M.J., Font, L., Altés, A., Muntañola, A., Bertazzoni, P., Rozman, M., Aymerich, M., Giné, E. & Montserrat, E. (2008) Fludarabine, cyclophosphamide, and mitoxantrone as initial therapy of chronic lymphocytic leukemia: high response rate and disease eradication. Clinical Cancer Research, 14, 155–161.
- Bosch, F., Abrisqueta, P., Villamoor, N., Terol, M.J., González-Barca, E., Ferra, C., González Diaz, M., Abella, E., Delgado, J., Carbonell, F., García Marco, J.A., Escoda, L., Ferrer, S., Monzó, E., González, Y., Estany, C., Jarque, I., Salamero, O., Muntañola, A. & Montserrat, E. (2009) Rituximab, fludarabine, cyclophosphamide and mitoxantrone: a new, highly active chemoimmunotherapy regiman for chronic lymphocytic leukamia. Journal of Clinical Oncology, 27, 4578–4584.
- Chen, B.P., Chan, D.W., Kobayashi, J., Burma, S., Asaithamby, A., Morotomi-Yano, K., Botvinick, E., Qin, J. & Chen, D.J. (2005) Cell cycle dependence of DNA-dependent protein kinase phosphorylation in response to DNA double strand breaks. Journal of Biological Chemistry, 280, 14709–14715.
- Cowell, I.G., Durkacz, B.W. & Tilby, M.J. (2005) Sensitization of breast carcinoma cells to ionizing radiation by small molecule inhibitors of DNA-dependent protein kinase and ataxia telangiectasia mutated. Biochemical Pharmacology, 71, 19–20.
- Deriano, L., Guipaud, O., Merle-Béral, H., Binet, J.L., Ricoul, M., Potocki-Veronese, G., Favaudon, V., Maciorowski, Z., Muller, C., Salles, B., Sabatier, L. & Delic, J. (2005) Human chronic lymphocytic leukemia B cells can escape DNA damage-induced apoptosis through the nonhomologous end-joining DNA repair pathway. Blood, 105, 4776–4783.
- Errington, F., Willmore, E., Tilby, M.J., Li, L., Li, G., Li, W., Baguley, B.C. & Austin, C.A. (1999) Murine transgenic cells lacking DNA topoisomerase IIbeta are resistant to acridines and mitoxantrone: analysis of cytotoxicity and cleavable complex formation. Molecular Pharmacology, 56, 1309–1316.
- Hardcastle, I.R., Cockcroft, X., Curtin, N.J., El- Murr, M.D., Leahy, J.J., Stockley, M., Golding, B.T., Rigoreau, L., Richardson, C., Smith, G.C. & Griffin, R.J. (2005) Discovery of potent chromen-4-one inhibitors of the DNA-dependent protein kinase (DNA-PK) using a small-molecule library approach. Journal of Medicinal Chemistry, 48, 7829–7846.
- Hewamana, S., Lin, T.T., Rowntree, C., Karunanithi, K., Pratt, G., Hills, R., Fegan, C., Brennan, P. & Pepper, C. (2009) Rel A is an independent biomarker of clinical outcome in chronic lymphocytic leukemia. Journal of Clinical Oncology, 27, 763–769.
- Kurtova, A.V., Balakrishnan, K., Chen, R., Ding, W., Schnabl, S., Quiroga, M.P., Sivina, M., Wierda, W.G., Estrov, Z., Keating, M.J., Shehata, M., Jäger, U., Gandhi, V., Kay, N.E., Plunkett, W. & Burger, J.A. (2009) Diverse marrow stromal cells protect CLL cells from spontaneous and drug-induced apoptosis: development of a reliable and reproducible system to assess stromal cell adhesion-mediated drug resistance. Blood, 114, 4441–4450.
- Lopez Guerra, M., Roué, G., Pérez-Galán, P., Alonso, R., Villamor, N., Montserrat, E., Campo, E. & Colomer, D. (2009) p65 Activity and ZAP-70 Status Predict the Sensitivity of Chronic Lymphocytic Leukemia Cells to the Selective IkB Kinase Inhibitor BMS-345541. Clinical Cancer Research, 15, 2767–2776.
- Matthews, C., Catherwood, M.A., Larkin, A.M., Clynes, M., Morris, T.C. & Alexander, H.D. (2006) MDR-1, but not MDR-3 gene expression, is associated with unmutated IGHV genes and poor prognosis chromosomal aberrations in chronic lymphocytic leukemia. Leukaemia & Lymphoma, 47, 2308–2313.
- Povirk, L.F., Zhou, R.Z., Ramsden, D.A., Lees- Miller, S.P. & Valerie, K. (2007) Phosphorylation in the serine/threonine 2609–2647 cluster promotes but is not essential for DNA-dependent protein kinase-mediated nonhomologous end joining in human whole-cell extracts. Nucleic Acids Research, 35, 3869–3878.
- Ribrag, V., Massade, L., Faussat, A.M., Dreyfus, F., Bayle, C., Gouyette, A. & Marie, J.P. (1996) Drug resistance mechanisms in chronic lymphocytic leukemia. Leukemia, 10, 1944–1949.
- Seiffert, M., Stilgenbauer, S., Döhner, H. & Lichter, P. (2007) Efficient nucleofection of primary human B cells and B-CLL cells induces apoptosis, which depends on the microenvironment and on the structure of transfected nucleic acids. Leukemia, 21, 1977–1983.
- Smart, D.J., Halicka, H.D., Schmuck, G., Traganos, F., Darzynkiewicz, Z. & Williams, G.M. (2008) Assessment of DNA double-strand breaks and gammaH2AX induced by the topoisomerase II poisons etoposide and mitoxantrone. Mutation Research, 641, 43–47.
- Stilgenbauer, S., Zenz, T., Winkler, D., Bühler, A., Busch, R., Fingerle-Rowson, G., Fischer, K., Fink, A.-M., Jäger, U., Böttcher, S., Kneba, M., Wenger, M., Mendila, M., Hallek, M. & Döhner, H. (2008) Genomic aberrations, VH mutation status and outcome after fludarabine and cyclophosphamide (FC) or FC plus rituximab (FCR) in the CLL8 trial. Blood (ASH Annual Meeting Abstracts), 112, 781.
- Toyoda, E., Kagaya, S., Cowell, I.G., Kurosawa, A., Kamoshita, K., Nishikawa, K., Iiizumi, S., Koyama, H., Austin, C.A. & Adachi, N. (2008) NK314, a Topoisomerase II Inhibitor that Specifically Targets the alpha isoform. Journal of Biological Chemistry, 283, 23711–23720.
- Uematsu, N., Weterings, E., Yano, K., Morotomi-Yano, K., Jakob, B., Taucher-Scholz, G., Mari, P.O., Van Gent, D.C., Chen, B.P. & Chen, D.J. (2007) Autophosphorylation of DNA-PKCS regulates its dynamics at DNA double-strand breaks. Journal of Cell Biology, 177, 219–229.
- Walker, J.V. & Nitiss, J.L. (2002) DNA topoisomerase II as a target for cancer chemotherapy. Cancer Investigation, 20, 570–589.
- Willmore, E., De Caux, S., Sunter, N.J., Tilby, M.J., Jackson, G.H., Austin, C.A. & Durkacz, B.W. (2004) A novel DNA-dependent protein kinase inhibitor, NU7026, potentiates the cytotoxicity of topoisomerase II poisons used in the treatment of leukemia. Blood, 103, 4659–4665.
- Willmore, E., Elliot, S.L., Mainou-Fowler, T., Summerfield, G.P., Jackson, G.H., O’Neill, F., Lowe, C., Carter, A., Harris, R., Pettitt, A.R., Cano-Soumillac, C., Griffin, R.J., Cowell, I.G., Austin, C.A. & Durkacz, B.W. (2008) DNA-dependent protein kinase is a therapeutic target and an indicator of poor prognosis in B-cell chronic lymphocytic leukemia. Clinical Cancer Research, 14, 3984–3992.
- Zenz, T., Kröber, A., Scherer, K., Häbe, S., Bühler, A., Benner, A., Denzel, T., Winkler, D., Edelmann, J., Schwänen, C., Döhner, H. & Stilgenbauer, S. (2008) Monoallelic TP53 inactivation is associated with poor prognosis in chronic lymphocytic leukemia: results from a detailed genetic characterization with long-term follow-up. Blood, 112, 3322–3329.
- Zhao, Y., Thomas, H.D., Batey, M.A., Cowell, I.G., Richardson, C.J., Griffin, R.J., Calvert, A.H., Newell, D.R., Smith, G.C. & Curtin, N.J. (2006) Preclinical evaluation of a potent novel DNA-dependent protein kinase inhibitor NU7441. Cancer Research, 66, 5354–5362.