PT  - JOURNAL ARTICLE
AU  - Kerstin Schmidt
AU  - Johannes Hoffend
AU  - Annette Altmann
AU  - Ludwig G. Strauss
AU  - Antonia Dimitrakopoulou-Strauss
AU  - Britta Engelhardt
AU  - Dirk Koczan
AU  - Jörg Peter
AU  - Thomas J. Dengler
AU  - Walter Mier
AU  - Michael Eisenhut
AU  - Uwe Haberkorn
AU  - Ralf Kinscherf
TI  - Angiostatin Overexpression in Morris Hepatoma Results in Decreased Tumor Growth but Increased Perfusion and Vascularization
DP  - 2006 Mar 01
TA  - Journal of Nuclear Medicine
PG  - 543--551
VI  - 47
IP  - 3
4099  - http://jnm.snmjournals.org/content/47/3/543.short
4100  - http://jnm.snmjournals.org/content/47/3/543.full
SO  - J Nucl Med2006 Mar 01; 47
AB  - Growth of malignant tumors is dependent on sufficient blood supply. Thus, inhibition of tumor angiogenesis is emerging as a promising target in the treatment of malignancies. Human angiostatin (hANG) is one of the most potent inhibitors of endothelial cell proliferation, angiogenesis, and tumor growth in vivo. However, its mechanisms operating in vivo are not well understood. Methods: To obtain more information about functional changes in the angiogenic process, we established Morris hepatoma (MH3924A) cell lines expressing hANG (hANG-MH3924A). The effects of hANG expression on proliferation and apoptosis of human umbilical vein endothelial cells (HUVECs) were measured in coculture experiments in vitro. To evaluate changes in tumor perfusion and blood volume, H215O and 68Ga-DOTA-albumin (DOTA is 1,4,7,10-tetraazacyclododecane-N,N′,N″,N‴-tetraacetic acid) were used for PET studies in vivo. Additionally, immunohistologic quantification of vascularization, apoptosis, and proliferation as well as gene array analyses were performed. Results: Our in vitro experiments demonstrate reduced proliferation and increased apoptosis in HUVECs when being cocultured with hANG-MH3924A. In support, tumor growth of hANG-MH3924A is diminished by 95% in vivo. However, tumor perfusion and blood volume are increased in hANG-MH3924A corresponding to an increased microvessel density. Furthermore, hANG-transfected tumors show changes in expression of genes related to apoptosis, stress, signal transduction, and metabolism. Conclusion: hANG expression leads to inhibition of tumor growth, increased apoptosis, and changes in the expression of multiple genes involved in stress reactions, signal transduction, and apoptosis, which indicates a multifactorial reaction of tumors. An enhanced microvessel density is seen as part of these reactions and is associated with increased perfusion as measured by PET.