Skip to main content
Top
Published in: Cancer Chemotherapy and Pharmacology 1/2012

01-01-2012 | Original Article

Preclinical anti-angiogenesis and anti-tumor activity of SIM010603, an oral, multi-targets receptor tyrosine kinases inhibitor

Authors: Dongchun Wang, Feng Tang, Sen Wang, Zhenzhou Jiang, Luyong Zhang

Published in: Cancer Chemotherapy and Pharmacology | Issue 1/2012

Login to get access

Abstract

Objective

SIM010603 is a structurally novel, oral, multi-targeted receptor tyrosine kinase inhibitor. This study investigated the anti-angiogenic and anti-tumor effects of SIM010603.

Methods

A radiometric protein kinase assay was used for measuring the kinase activity of the 32 protein kinases. Receptor phosphorylation was determined by enzyme-linked immunosorbent assay (ELISA). Cell proliferation was measured by 3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay. Cell chemotaxis was evaluated by modified Boyden chamber assay. Effect of SIM010603 on angiogenesis was examined by mouse cornea angiogenesis assay. Effect of SIM010603 on xenografts was assessed by tumor growth delay. Effects of SIM010603 on tumor microvascular density (MVD), recruitment of pericytes, and pericyte encapsulation of tumor vessels were analyzed by immunofluorescent staining technique.

Results

SIM010603 inhibited stem cell factor receptor (Kit), vascular endothelial growth factor receptor-2 (VEGFR-2), platelet-derived growth factor receptor-β (PDGFR-β), glial cell line-derived neurotrophic factor receptor (Rearranged during Transfection; RET), and Fms-like tyrosine kinase-3 (FLT3) with IC50 values between 5.0 and 68.1 nmol/l. SIM010603 inhibited the phosphorylation of PDGFR-β and VEGFR-2. Moreover, SIM010603 inhibited endothelial cell proliferation, endothelial cells chemotaxis, and corneal angiogenesis. Although SIM010603 exhibited lower activity in regard to proliferation of NCI-H460, MDA-MB-435, and T241-VEGF-A cells (IC50 > 1 μmol/l), SIM010603 inhibited tumor growth in these xenograft tumor growth models. SIM010603 reduced tumor MVD in T241-VEGF-A tumor xenograft models and decreased positive signals of CD31, NG2 in MDA-MB-435, and LLC-SW-44 xenograft tumor models.

Conclusions

These results support the clinical assessment of SIM010603 as a therapeutic agent for cancer.
Appendix
Available only for authorised users
Literature
1.
go back to reference Gatzemeier U, Blumenschein G, Fosella F, Simantov R, Elting J, Bigwood D et al (2006) Phase II trial of single-agent sorafenib in patients with advanced non-small cell lung carcinoma. J Clin Oncol 24(Suppl):364s Gatzemeier U, Blumenschein G, Fosella F, Simantov R, Elting J, Bigwood D et al (2006) Phase II trial of single-agent sorafenib in patients with advanced non-small cell lung carcinoma. J Clin Oncol 24(Suppl):364s
2.
go back to reference Hurwitz H, Fehrenbacher L, Novotny W, Cripe L, McGuire W, Wertheim M et al (2007) Integrated report of the phase 2 experience with XL999 administered IV to patients (pts) with NSCLC, renal cell CA (RCC), metastatic colorectal CA (CRC), recurrent ovarian CA, acute myelogenousleuk aemia (AML), and multiple myeloma (MM). J Clin Oncol 25(Suppl):160s Hurwitz H, Fehrenbacher L, Novotny W, Cripe L, McGuire W, Wertheim M et al (2007) Integrated report of the phase 2 experience with XL999 administered IV to patients (pts) with NSCLC, renal cell CA (RCC), metastatic colorectal CA (CRC), recurrent ovarian CA, acute myelogenousleuk aemia (AML), and multiple myeloma (MM). J Clin Oncol 25(Suppl):160s
3.
go back to reference Ross RW, Stein M, Sarantopoulos J, Eisenberg P, Logan T, Srinivas S et al (2007) A phase II study of the c-Met RTK inhibitor XL880 in patients (pts) with papillary renal-cell carcinoma (PRC). J Clin Oncol 25(Suppl):658s Ross RW, Stein M, Sarantopoulos J, Eisenberg P, Logan T, Srinivas S et al (2007) A phase II study of the c-Met RTK inhibitor XL880 in patients (pts) with papillary renal-cell carcinoma (PRC). J Clin Oncol 25(Suppl):658s
4.
go back to reference Tibes R, Trent J, Kurzrock R (2005) Tyrosine kinase inhibitors and the dawn of molecular cancer therapeutics. Ann Rev Pharmacol Toxicol 45:357–384CrossRef Tibes R, Trent J, Kurzrock R (2005) Tyrosine kinase inhibitors and the dawn of molecular cancer therapeutics. Ann Rev Pharmacol Toxicol 45:357–384CrossRef
7.
go back to reference Shah NP, Nicoll JM, Nagar B, Gorre ME, Paquette RL, Kuriyan J et al (2002) Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia. Cancer Cell 2:117–125PubMedCrossRef Shah NP, Nicoll JM, Nagar B, Gorre ME, Paquette RL, Kuriyan J et al (2002) Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia. Cancer Cell 2:117–125PubMedCrossRef
8.
go back to reference Pao W, Miller V, Zakowski M, Doherty J, Politi K, Sarkaria I et al (2004) EGF receptor gene mutations are common in lung cancers from “never smokers” and are associated with sensitivity of tumors to gefitinib and erlotinib. Proc Natl Acad Sci 101:13306–13311PubMedCrossRef Pao W, Miller V, Zakowski M, Doherty J, Politi K, Sarkaria I et al (2004) EGF receptor gene mutations are common in lung cancers from “never smokers” and are associated with sensitivity of tumors to gefitinib and erlotinib. Proc Natl Acad Sci 101:13306–13311PubMedCrossRef
9.
go back to reference Baselga J, Arteaga CL (2005) Critical update and emerging trends in epidermal growth factor receptor targeting in cancer. J Clin Oncol 23:2445–2459PubMedCrossRef Baselga J, Arteaga CL (2005) Critical update and emerging trends in epidermal growth factor receptor targeting in cancer. J Clin Oncol 23:2445–2459PubMedCrossRef
10.
go back to reference Paez JG, Janne PA, Lee JC, Tracy S, Greulich H, Gabriel S et al (2004) EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy. Science 304:1497–1500PubMedCrossRef Paez JG, Janne PA, Lee JC, Tracy S, Greulich H, Gabriel S et al (2004) EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy. Science 304:1497–1500PubMedCrossRef
11.
go back to reference Petrelli A, Giordano S (2008) From single- to multi-target drugs in cancer therapy: when aspecificity becomes an advantage. Curr Med Chem 15(5):422–432PubMedCrossRef Petrelli A, Giordano S (2008) From single- to multi-target drugs in cancer therapy: when aspecificity becomes an advantage. Curr Med Chem 15(5):422–432PubMedCrossRef
12.
go back to reference Ocanal A, Serrano R, Calero R, Pandiella A (2009) Novel tyrosine kinase inhibitors in the treatment of cancer. Curr Drug Targets 10(6):575–576CrossRef Ocanal A, Serrano R, Calero R, Pandiella A (2009) Novel tyrosine kinase inhibitors in the treatment of cancer. Curr Drug Targets 10(6):575–576CrossRef
13.
go back to reference Cao R, Xue Y, Hedlund EM, Zhong Zh, Tritsaris K, Tondelli B, Lucchini F et al (2010) VEGFR1—mediated pericyte ablation links VEGF and PlGF to cancer-associated retinopathy. Proc Natl Acad Sci 107:856–861PubMedCrossRef Cao R, Xue Y, Hedlund EM, Zhong Zh, Tritsaris K, Tondelli B, Lucchini F et al (2010) VEGFR1—mediated pericyte ablation links VEGF and PlGF to cancer-associated retinopathy. Proc Natl Acad Sci 107:856–861PubMedCrossRef
14.
go back to reference Hedlund EM, Hosaka K, Zhong ZH, Cao R, Cao Y (2009) Malignant cell-derived PlGF promotes normalization and remodeling of the tumor vasculature. Proc Natl Acad Sci 106:17505–17510PubMedCrossRef Hedlund EM, Hosaka K, Zhong ZH, Cao R, Cao Y (2009) Malignant cell-derived PlGF promotes normalization and remodeling of the tumor vasculature. Proc Natl Acad Sci 106:17505–17510PubMedCrossRef
15.
go back to reference Sanghera J, Li R, Yan J (2009) Comparison of the luminescent ADP-Glo assay to a standard radiometric assay for measurement of protein kinase activity. Assay Drug Dev Technol 7(6):615–622PubMedCrossRef Sanghera J, Li R, Yan J (2009) Comparison of the luminescent ADP-Glo assay to a standard radiometric assay for measurement of protein kinase activity. Assay Drug Dev Technol 7(6):615–622PubMedCrossRef
16.
go back to reference Roberts WG, Whalen PM, Soderstrom E, Moraski G, Lyssikatos JP, Wang HF et al (2005) Antiangiogenic and antitumor activity of a selective PDGFR tyrosine kinase inhibitor, CP-673, 451. Cancer Res 65(3):957–966PubMed Roberts WG, Whalen PM, Soderstrom E, Moraski G, Lyssikatos JP, Wang HF et al (2005) Antiangiogenic and antitumor activity of a selective PDGFR tyrosine kinase inhibitor, CP-673, 451. Cancer Res 65(3):957–966PubMed
17.
go back to reference Cao Y, Linden P, Farnebo J, Cao R, Eriksson A, Kumar V et al (1998) Vascular endothelial growth factor C induces angiogenesis in vivo. Proc Natl Acad Sci 95:14389–14394PubMedCrossRef Cao Y, Linden P, Farnebo J, Cao R, Eriksson A, Kumar V et al (1998) Vascular endothelial growth factor C induces angiogenesis in vivo. Proc Natl Acad Sci 95:14389–14394PubMedCrossRef
18.
go back to reference Labrecque L, Lamy S, Chapus A, Mihoubi S, Durocher Y, Cass B et al (2005) Combined inhibition of PDGF and VEGF receptors by ellagic acid, a dietary-derived phenolic compound. Carcinogenesis 26:821–826PubMedCrossRef Labrecque L, Lamy S, Chapus A, Mihoubi S, Durocher Y, Cass B et al (2005) Combined inhibition of PDGF and VEGF receptors by ellagic acid, a dietary-derived phenolic compound. Carcinogenesis 26:821–826PubMedCrossRef
19.
go back to reference Cao R, Brakenhielm E, Wahlestedt C, Thyberg J, Cao Y (2001) Leptin induces vascular permeability and synergistically stimulates angiogenesis with FGF-2 and VEGF. Proc Natl Acad Sci 98:6390–6395PubMedCrossRef Cao R, Brakenhielm E, Wahlestedt C, Thyberg J, Cao Y (2001) Leptin induces vascular permeability and synergistically stimulates angiogenesis with FGF-2 and VEGF. Proc Natl Acad Sci 98:6390–6395PubMedCrossRef
20.
go back to reference Leung DW, Cachianes G, Kuang WJ, Goeddel DV, Ferrara N (1989) Vascular endothelial growth factor is a secreted angiogenic mitogen. Science 246:1306–1309PubMedCrossRef Leung DW, Cachianes G, Kuang WJ, Goeddel DV, Ferrara N (1989) Vascular endothelial growth factor is a secreted angiogenic mitogen. Science 246:1306–1309PubMedCrossRef
22.
go back to reference Chen F, Xue Y, Cao Y, Han B (2009) Cancer-associated systemic syndrome (CASS): the mechanism of VEGF in tumor-bearing mice. Chin J Lung Cancer 12(4):30–35 Chen F, Xue Y, Cao Y, Han B (2009) Cancer-associated systemic syndrome (CASS): the mechanism of VEGF in tumor-bearing mice. Chin J Lung Cancer 12(4):30–35
23.
go back to reference Xue Y, Religa P, Cao R, Hansen AJ, Lucchini F, Jones B et al (2008) Anti-VEGF agents confer survival advantages to tumor-bearing mice by improving cancer-associated systemic syndrome. Proc Natl Acad Sci 105(47):18513–18518PubMedCrossRef Xue Y, Religa P, Cao R, Hansen AJ, Lucchini F, Jones B et al (2008) Anti-VEGF agents confer survival advantages to tumor-bearing mice by improving cancer-associated systemic syndrome. Proc Natl Acad Sci 105(47):18513–18518PubMedCrossRef
24.
go back to reference Sun L, Tran N, Tang F, App H, Hirth P, McMahon G et al (1998) Synthesis and biological evaluations of 3-substituted indolin-2-ones: a novel class of tyrosine kinase inhibitors that exhibit selectivity toward particular receptor tyrosine kinases. J Med Chem 41(14):2588–2603PubMedCrossRef Sun L, Tran N, Tang F, App H, Hirth P, McMahon G et al (1998) Synthesis and biological evaluations of 3-substituted indolin-2-ones: a novel class of tyrosine kinase inhibitors that exhibit selectivity toward particular receptor tyrosine kinases. J Med Chem 41(14):2588–2603PubMedCrossRef
25.
go back to reference Mendel DB, Laird AD, Xin X, Louie SG, Christensen JG, Schreck RE et al (2003) In vivo antitumor activity of SU11248, a novel tyrosine kinase inhibitor targeting vascular endothelial growth factor and platelet-derived growth factor receptors: determination of a pharmacokinetic/pharmacodynamic relationship. Clin Cancer Res 9:327–337PubMed Mendel DB, Laird AD, Xin X, Louie SG, Christensen JG, Schreck RE et al (2003) In vivo antitumor activity of SU11248, a novel tyrosine kinase inhibitor targeting vascular endothelial growth factor and platelet-derived growth factor receptors: determination of a pharmacokinetic/pharmacodynamic relationship. Clin Cancer Res 9:327–337PubMed
26.
go back to reference O’Farrell AM, Abrams TJ, Yuen HA, Ngai TJ, Louie SG, Yee KWH et al (2003) SU11248 is a novel FLT3 tyrosine kinase inhibitor with potent activity in vitro and in vivo. Blood 101:3597–3605PubMedCrossRef O’Farrell AM, Abrams TJ, Yuen HA, Ngai TJ, Louie SG, Yee KWH et al (2003) SU11248 is a novel FLT3 tyrosine kinase inhibitor with potent activity in vitro and in vivo. Blood 101:3597–3605PubMedCrossRef
27.
go back to reference SUTENT (sunitinibmalate) prescribing information (2006) Pfizer. Inc., New York SUTENT (sunitinibmalate) prescribing information (2006) Pfizer. Inc., New York
28.
go back to reference Mohammadi M, McMahon G, Sun L, Tang C, Hirth P, Yeh BK, Hubbard SR et al (1997) Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitors. Science 276:955–960PubMedCrossRef Mohammadi M, McMahon G, Sun L, Tang C, Hirth P, Yeh BK, Hubbard SR et al (1997) Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitors. Science 276:955–960PubMedCrossRef
29.
go back to reference Sun L, Tran N, Liang C, Tang F, Rice A, Schreck R et al (1999) Design, synthesis, and evaluations of substituted 3-[(3- or 4-carboxyethylpyrrol-2-yl)methylidenyl]indolin-2-ones as inhibitors of VEGF, FGF, and PDGF receptor tyrosine kinases. J Med Chem 42(5):5120–5130PubMedCrossRef Sun L, Tran N, Liang C, Tang F, Rice A, Schreck R et al (1999) Design, synthesis, and evaluations of substituted 3-[(3- or 4-carboxyethylpyrrol-2-yl)methylidenyl]indolin-2-ones as inhibitors of VEGF, FGF, and PDGF receptor tyrosine kinases. J Med Chem 42(5):5120–5130PubMedCrossRef
30.
31.
go back to reference Andrae J, Gallini R, Betsholtz C (2008) Role of platelet-derived growth factors in physiology and medicine. Genes Dev 22:1276–1312PubMedCrossRef Andrae J, Gallini R, Betsholtz C (2008) Role of platelet-derived growth factors in physiology and medicine. Genes Dev 22:1276–1312PubMedCrossRef
32.
go back to reference Zhang XH, Lin LP, Ding J (2006) Platelet-derived growth factor receptor and cancer. Chin Bull Life Sci 18(3):220–226 Zhang XH, Lin LP, Ding J (2006) Platelet-derived growth factor receptor and cancer. Chin Bull Life Sci 18(3):220–226
33.
go back to reference Tallquist M, Kazlauskas A (2004) PDGF signaling in cells and mice. Cytokine Growth Factor Rev 15(4):205–213PubMedCrossRef Tallquist M, Kazlauskas A (2004) PDGF signaling in cells and mice. Cytokine Growth Factor Rev 15(4):205–213PubMedCrossRef
34.
go back to reference Vincent L, Rafii S (2004) Vascular frontiers without borders: multifaceted roles of platelet-derived growth factor (PDGF) in supporting postnatal angiogenesis and lymphangiogenesis. Cancer Cell 6:307–309PubMedCrossRef Vincent L, Rafii S (2004) Vascular frontiers without borders: multifaceted roles of platelet-derived growth factor (PDGF) in supporting postnatal angiogenesis and lymphangiogenesis. Cancer Cell 6:307–309PubMedCrossRef
35.
go back to reference Yao VJ, Sennino B, Davis RB et al (2006) Combined anti-VEGFR and anti-PDGFR actions of sunitinib on blood vessels in preclinical tumor models. Presented at the 18th EORTC–NCI–AACR symposium, Prague, Czech Republic, 7–10 November 2006 Yao VJ, Sennino B, Davis RB et al (2006) Combined anti-VEGFR and anti-PDGFR actions of sunitinib on blood vessels in preclinical tumor models. Presented at the 18th EORTC–NCI–AACR symposium, Prague, Czech Republic, 7–10 November 2006
Metadata
Title
Preclinical anti-angiogenesis and anti-tumor activity of SIM010603, an oral, multi-targets receptor tyrosine kinases inhibitor
Authors
Dongchun Wang
Feng Tang
Sen Wang
Zhenzhou Jiang
Luyong Zhang
Publication date
01-01-2012
Publisher
Springer-Verlag
Published in
Cancer Chemotherapy and Pharmacology / Issue 1/2012
Print ISSN: 0344-5704
Electronic ISSN: 1432-0843
DOI
https://doi.org/10.1007/s00280-011-1681-1

Other articles of this Issue 1/2012

Cancer Chemotherapy and Pharmacology 1/2012 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine