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Potent and sustained inhibition of HIF-1α and downstream genes by a polyethyleneglycol-SN38 conjugate, EZN-2208, results in anti-angiogenic effects.
- Source :
-
Angiogenesis [Angiogenesis] 2011 Sep; Vol. 14 (3), pp. 245-53. Date of Electronic Publication: 2011 Mar 31. - Publication Year :
- 2011
-
Abstract
- Topoisomerase I inhibitors down-regulate HIF-1α leading to tumor growth inhibition, but only while maintaining sustained levels of drug exposure. EZN-2208, a multi-arm 40 kDa pegylated, releasable SN38-drug conjugate, provides higher, longer lasting exposure of tumors to SN38 in contrast to SN38 that is released from CPT-11. EZN-2208 also consistently has greater antitumor activity than CPT-11 in a variety of solid and hematological tumor models. In this report, the ability of PEG-SN38 to down-regulate HIF-1α and its downstream targets, in a more potent, sustained manner compared with CPT-11 was examined. To do so, U251 glioma xenografts that stably expressed a hypoxia response element-dependent luciferase reporter gene were implanted in mice. After treatment it was found that EZN-2208 induced potent, sustained HIF-1α down-regulation (37% at 48 h and 83% at 120 h) in the tumors, whereas CPT-11 caused only minor, transient HIF-1α down-regulation. In addition, EZN-2208 down-regulated mRNA levels of HIF-1α targeted genes (MMP2, VEGF1, Glut1, Glut3 and TGFβ1). Further, western blot analyses of xenograft tumors demonstrated that EZN-2208 had significantly more effect than CPT-11 in down-regulating HIF-1α, VEGF, Glut1 and MMP2 protein levels. Significant down-regulation of HIF-1α and VEGF proteins translated to EZN-2208's superior anti-angiogenic activity compared with CPT-11, confirmed by microvessel density reduction in a chorioallantoic membrane assay and in CD-31 immunohistochemistry studies. Additional studies done with matrigel implants devoid of tumor cells show that EZN-2208 significantly inhibits angiogenesis while CPT-11 has little or no effect. It is concluded that the superior antitumor activity of EZN-2208 compared with CPT-11 is attributed, in part, to an anti-angiogenic effect. Ongoing clinical Phase I and Phase II studies will assess safety and efficacy of EZN-2208.
- Subjects :
- Animals
Antineoplastic Agents, Phytogenic pharmacology
Camptothecin pharmacology
Cell Line, Tumor
Glioma metabolism
Glioma pathology
Humans
Irinotecan
Mice
Mice, Nude
Neovascularization, Pathologic metabolism
Neovascularization, Pathologic pathology
Xenograft Model Antitumor Assays
Angiogenesis Inhibitors pharmacology
Camptothecin analogs & derivatives
Down-Regulation drug effects
Gene Expression Regulation, Neoplastic drug effects
Glioma drug therapy
Hypoxia-Inducible Factor 1, alpha Subunit biosynthesis
Neoplasm Proteins biosynthesis
Neovascularization, Pathologic drug therapy
Polyethylene Glycols pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1573-7209
- Volume :
- 14
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Angiogenesis
- Publication Type :
- Academic Journal
- Accession number :
- 21452059
- Full Text :
- https://doi.org/10.1007/s10456-011-9209-1