[Show abstract][Hide abstract] ABSTRACT: Angiogenesis plays an important role in tumor growth and metastasis, therefore antiangiogenic therapy was widely investigated as a promising approach for cancer therapy. Recently, pigment epithelium-derived factor (PEDF) has been shown to be the most potent inhibitor of angiogenesis. Adeno-associated virus (AAV) vectors have been intensively studied due to their wide tropisms, nonpathogenicity, and long-term transgene expression in vivo. The objective of this work was to evaluate the ability of AAV-mediated human PEDF (hPEDF) as a potent tumor suppressor and a potential candidate for cancer gene therapy.
Recombinant AAV2 encoding hPEDF (rAAV2-hPEDF) was constructed and produced, and then was assigned for in vitro and in vivo experiments. Conditioned medium from cells infected with rAAV2-hPEDF was used for cell proliferation and tube formation tests of human umbilical vein endothelial cells (HUVECs). Subsequently, colorectal peritoneal carcinomatosis (CRPC) mouse model was established and treated with rAAV2-hPEDF. Therapeutic efficacy of rAAV2-hPEDF were investigated, including tumor growth and metastasis, survival time, microvessel density (MVD) and apoptosis index of tumor tissues, and hPEDF levels in serum and ascites.
rAAV2-hPEDF was successfully constructed, and transmission electron microscope (TEM) showed that rAAV2-hPEDF particles were non-enveloped icosahedral shape with a diameter of approximately 20 nm. rAAV2-hPEDF-infected cells expressed hPEDF protein, and the conditioned medium from infected cells inhibited proliferation and tube-formation of HUVECs in vitro. Furthermore, in CRPC mouse model, rAAV2-hPEDF significantly suppressed tumor growth and metastasis, and prolonged survival time of treated mice. Immunofluorescence studies indicated that rAAV2-hPEDF could inhibit angiogenesis and induce apoptosis in tumor tissues. Besides, hPEDF levels in serum and ascites of rAAV2-hPEDF-treated mice were significant higher than those in rAAV2-null or normal saline (NS) groups.
Thus, our results suggest that rAAV2-hPEDF may be a potential candidate as an antiangiogenic therapy agent.
BMC Cancer 03/2012; 12(1):129. DOI:10.1186/1471-2407-12-129 · 3.36 Impact Factor
[Show abstract][Hide abstract] ABSTRACT: The accumulation and elimination kinetics for Cd described by one-compartment model were determined in five subcellular fractions of wheat after exposure to 5.0 μM Cd with or without pre-exposure to 0.1 μM Cd or 5.0 μM Zn. The results show that the acclimation of wheat to Cd or Zn generates its resistance to Cd and decreased Cd accumulation in wheat. The acclimation of wheat to Cd or Zn enhanced the accumulation of Cd in the biological detoxified fractions especially the heat-stable fraction and decreased the accumulation of Cd in the metal sensitive fractions especially the heat-denatured proteins over time. Subsequently, the acclimation to Cd or Zn increased the activities of CAT and SOD in root and shoot to different extents compared to the unacclimated wheat. This study for the first time suggests that the acclimation of plant to low-level metal affects the accumulation and the toxicity of metal in plant.