Literature DB >> 20570929

The vascular endothelial growth factor receptor tyrosine kinase inhibitors vatalanib and pazopanib potently induce apoptosis in chronic lymphocytic leukemia cells in vitro and in vivo.

Julian Paesler1, Iris Gehrke, Rajesh Kumar Gandhirajan, Alexandra Filipovich, Magdalena Hertweck, Felix Erdfelder, Sabrina Uhrmacher, Simon Jonas Poll-Wolbeck, Michael Hallek, Karl-Anton Kreuzer.   

Abstract

PURPOSE: There is evidence that vascular endothelial growth factor (VEGF) is a critical microenvironmental factor that exerts angiogenesis-independent effects on the survival of chronic lymphocytic leukemia (CLL) cells. Vatalanib and pazopanib are potent orally available VEGF receptor tyrosine kinase inhibitors. We investigated the efficacy and selectivity of both compounds in CLL cells, simulated potential combination with conventional cytostatics, and tested the effect of both substances on CLL-like tumor xenografts. EXPERIMENTAL
DESIGN: Primary CLL and normal peripheral blood cells were tested for viability after incubation with varying concentrations of both inhibitors. Further, phosphorylation status of VEGF receptor on treatment, caspase activation, and poly(ADP-ribose) polymerase cleavage were assessed. Combinations of each inhibitor with fludarabine, vincristine, and doxorubicin were analyzed for possible synergistic effects in vitro. For in vivo testing, mice grafted with the CLL-like cell line JVM-3 were treated orally with each inhibitor.
RESULTS: Vatalanib and pazopanib decreased phosphorylation of the VEGF receptor, along with induction of apoptosis in CLL cells in clinically achievable concentrations. Healthy B cells were only mildly affected. Immunoblots showed downregulation of the antiapoptotic proteins XIAP and MCL1, whereas poly(ADP-ribose) polymerase cleavage was increased. Combinations with conventional cytostatic agents resulted in synergistic effects. Treatment of xenografted mice with 100 mg/kg of body weight for 21 days resulted in tumor inhibition rates of 76% (vatalanib) and 77% (pazopanib). In two mice, a total tumor eradication could be observed. No gross systemic toxicity occurred.
CONCLUSION: We conclude that VEGF inhibition is a promising new therapeutic approach in CLL. Vatalanib and pazopanib seem to be effective and safe candidates to be further evaluated for this purpose.

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Year:  2010        PMID: 20570929     DOI: 10.1158/1078-0432.CCR-10-0232

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  23 in total

1.  Bone marrow stromal cell-derived vascular endothelial growth factor (VEGF) rather than chronic lymphocytic leukemia (CLL) cell-derived VEGF is essential for the apoptotic resistance of cultured CLL cells.

Authors:  Iris Gehrke; Rajesh Kumar Gandhirajan; Simon Jonas Poll-Wolbeck; Michael Hallek; Karl-Anton Kreuzer
Journal:  Mol Med       Date:  2011-04-14       Impact factor: 6.354

Review 2.  Critical signal transduction pathways in CLL.

Authors:  Asish K Ghosh; Neil E Kay
Journal:  Adv Exp Med Biol       Date:  2013       Impact factor: 2.622

3.  A Phase II Study of Pazopanib in Patients with Malignant Pleural Mesothelioma: NCCTG N0623 (Alliance).

Authors:  Kaushal Parikh; Sumithra J Mandrekar; Katie Allen-Ziegler; Brandt Esplin; Angelina D Tan; Benjamin Marchello; Alex A Adjei; Julian R Molina
Journal:  Oncologist       Date:  2019-12-24

4.  α4β1 integrin associates with VEGFR2 in CLL cells and contributes to VEGF binding and intracellular signaling.

Authors:  Alejandra Gutiérrez-González; Noemí Aguilera-Montilla; Estefanía Ugarte-Berzal; Elvira Bailón; Isabel Cerro-Pardo; Clara Sánchez-Maroto; Lara García-Campillo; José A García-Marco; Angeles García-Pardo
Journal:  Blood Adv       Date:  2019-07-23

5.  Effects of inhibitors of vascular endothelial growth factor receptor 2 and downstream pathways of receptor tyrosine kinases involving phosphatidylinositol 3-kinase/Akt/mammalian target of rapamycin or mitogen-activated protein kinase in canine hemangiosarcoma cell lines.

Authors:  Mami Adachi; Yuki Hoshino; Yusuke Izumi; Hiroki Sakai; Satoshi Takagi
Journal:  Can J Vet Res       Date:  2016-07       Impact factor: 1.310

6.  Phase II trials of single-agent anti-VEGF therapy for patients with chronic lymphocytic leukemia.

Authors:  Tait Shanafelt; Clive Zent; John Byrd; Charles Erlichman; Betsy Laplant; Asish Ghosh; Timothy Call; Miguel Villalona-Calero; Diane Jelinek; Deborah Bowen; Kristina Laumann; Wenting Wu; Curtis Hanson; Neil Kay
Journal:  Leuk Lymphoma       Date:  2010-11-05

7.  The novel receptor tyrosine kinase Axl is constitutively active in B-cell chronic lymphocytic leukemia and acts as a docking site of nonreceptor kinases: implications for therapy.

Authors:  Asish K Ghosh; Charla Secreto; Justin Boysen; Traci Sassoon; Tait D Shanafelt; Debabrata Mukhopadhyay; Neil E Kay
Journal:  Blood       Date:  2010-12-06       Impact factor: 22.113

8.  Sorafenib-induced apoptosis of chronic lymphocytic leukemia cells is associated with downregulation of RAF and myeloid cell leukemia sequence 1 (Mcl-1).

Authors:  Jessie-F Fecteau; Ila S Bharati; Morgan O'Hayre; Tracy M Handel; Thomas J Kipps; Davorka Messmer
Journal:  Mol Med       Date:  2012-02-10       Impact factor: 6.354

Review 9.  Overview of fundamental study of pazopanib in cancer.

Authors:  Hong-Lin Zhao; Fan Yang; Xin Huang; Qing-Hua Zhou
Journal:  Thorac Cancer       Date:  2014-10-23       Impact factor: 3.500

10.  Cell death signaling and anticancer therapy.

Authors:  Lorenzo Galluzzi; Ilio Vitale; Erika Vacchelli; Guido Kroemer
Journal:  Front Oncol       Date:  2011-05-03       Impact factor: 6.244

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