

FOLLOWUS
1. Medical College Qingdao University
2. Yellow Sea Fisheries Research Institute Chinese Academy of Fishery Sciences
Online First:04 December 2009,
Published:2009
Scan QR Code
Wang, Z., Liu, J., Su, A. et al. Antiangiogenic activity of low-temperature lysozyme from a marine bacterium in vivo and in vitro, ., Chin. J. Ocean. Limnol. 27, 835–844 (2009). https://doi.org/10.1007/s00343-009-9181-4
We extracted marine low-temperature lysozyme (MLTL)
a novel lysozyme
from a marine microorganism through fermentation. Our previous study suggested that a low molecular weight (16 kDa) may exert anti-tumor activity through antiangiogenesis. In this study
we extracted a high weight (39 kDa) and investigated its antiangiogenic activity in vivo and in vitro. Using zebrafish embryos as an in vivo study model
we found that treatment with MLTL significantly inhibited the growth of subintestinal vessels (SIVs) in a dose-dependent manner and that 400 µg/ml MLTL was sufficient to block the growth of SIVs. An in vitro study conducted using human umbilical vein endothelial cells (HUVECs) revealed that MLTL suppressed the proliferation
migration and tube formation of HUVECs in a dose-dependent manner. Interestingly
assays by flow cytometry and DNA electrophoresis indicated that MLTL was able to induce apoptosis of HUVECs. Moreover
further study demonstrated that the disruption of intracellular Ca2+ homeostasis may play an important role in MLTL induced apoptosis of HUVECs. Taken together
the results of this study demonstrate for the first time that MLTL inhibits angiogenesis through its pleiotropic effects on vascular endothelial cells and induces apoptosis through regulation of cellular Ca2+ levels. The results of this study also revealed a possible mechanism underlying the antiangiogenic effect of MLTL and suggested that MLTL may be a promising new antiangiogenic agent for use in cancer therapy.
Amador M L, Jimeno J, Paz-Ares L, Cortes-Funes H, Hidalgo M. 2003. Progress in the development and acquisition of anticancer agents from marine sources. Ann. Oncol. 14(11): 1 607–1 615.
Amino N, Ideyama Y, Yamano M, Kuromitsu S, Tajinda K, Samizu K, Matsuhisa A, Shirasuna K, Kudoh M, Shibasaki M. 2005. YM-231146, a novel orally bioavailable inhibitor of vascular endothelial growth factor receptor-2, is effective against paclitaxel resistant tumors. Biol. Pharm. Bull., 28(11): 2 096–2 101.
Bergamaschi G, Rosti V, Danova M, Lucotti C, Cazzola M. 1994. Apoptosis: biological and clinical aspects. Haematologica, 79(1): 86–93.
Blake C, Koening D. 1965. Structure of hen egg white lysozyme. Nature, 206: 757–761.
Distler J H, Hirth A, Kurowska-Stolarska M, Gay R E, Gay S, Distler O. 2003. Angiogenic and angiostatic factors in the molecular control of angiogenesis. Q. J. Nucl. Med., 47(3): 149–161.
Folkman J. 2003. Angiogenesis and apoptosis. Semin. Cancer Biol., 13(2): 159–167.
Fouquet B, Weinstein B M, Serluca F C, Fishman M C. 1997. Vessel patterning in the embryo of the zebrafish: guidance by notochord. Dev. Biol., 183(1): 37–48.
Furuya Y, Lundmo P, Short A D, Gill D L, Isaacs J T. 1994. The role of calcium, pH, and cell proliferation in the programmed (apoptotic) death of androgen-independent prostatic cancer cells induced by thapsigargin. Cancer Res., 54(23): 6 167–6 175.
Hou W H, Wang T Y, Yuan B M, Chai Y R, Jia Y L, Tian F, Wang J M, Xue L X. 2004. Recombinant mouse canstatin inhibits chicken embryo chorioallantoic membrane angiogenesis and endothelial cell proliferation. Acta Biochim. Biophys. Sin., 36(12): 845–850.
Kim Y M, Namkoong S, Yun Y G, Hong H D, Lee Y C, Ha K S, Lee H, Kwon H J, Kwon Y G, Kim Y M. 2007. Water extract of Korean red ginseng stimulates angiogenesis by activating the PI3K/Akt-dependent ERK1/2 and eNOS pathways in human umbilical vein endothelial cells. Biol. Pharm. Bull., 30(9): 1 674–1 679.
Kleinman H K, Liau G. 2001. Gene therapy for antiangiogenesis. J. Natl. Cancer Inst., 93(13): 965–967.
Ling Y, Yang Y, Lu N, You Q D, Wang S, Gao Y, Chen Y, Guo Q L. 2007. Endostar, a novel recombinant human endostatin, exerts antiangiogenic effect via blocking VEGF-induced tyrosine phosphorylation of KDR/Flk-1 of endothelial cells. Biochem. Biophys. Res. Commun., 361(1): 79–84.
Nilsen I W, Myrnes B. 2001. The gene of chlamysin, a marine invertebrate-type lysozyme, is organized similar to vertebrate but different from invertebrate chicken-type lysozyme genes. Gene, 69(1–2): 27–32.
Nilsen I W, Overbo K, Sandsdalen E. Sandaker E, Sletten K, Myrnes B. 1999. Protein purification and gene isolation of chlamysin, a cold-active lysozyme-like enzyme with antibacterial activity. FEBS. Lett., 464(3): 153–158.
Norrby K. 2006. In vivo models of angiogenesis. J. Cell Mol. Med., 10(3): 588–612.
Patel S, Leal A D, Gorski D H. 2005. The homeobox gene Gax inhibits angiogenesis through inhibition of nuclear factor-βB-dependent endothelial cell gene expression. Cancer Res., 65(4): 1 414–1 424.
Pinton P, Rizzuto R. 2006. Bcl-2 and Ca2+ homeostasis in the endoplasmic reticulum. Cell Death Differen., 13(8):1 409–1 418.
Roberts W G, Whalen P M, Soderstrom E, Moraski G, Lyssikatos J P, Wang H F, Cooper B, Baker D A, Savage D, Dalvie D, Atherton J A, Ralston S, Szewc R, Kath J C, J. Lin, Soderstrom C Y, Tkalcevic G, Cohen B D, Pollack V, Barth W, Hungerford W, Ung E. 2005. Antiangiogenic and antitumor activity of a selective PDGFR tyrosine kinase inhibitor, CP-673,451. Cancer Res., 65(3): 957–966.
Shimizu K, Oku N. 2004. Cancer anti-angiogenic therapy. Biol. Pharm. Bull., 27(5): 599–605.
Simmons T L, Andrianasolo E, McPhail K, Flatt P, Gerwick W H. 2005. Marine natural products as anticancer drugs. Mol. Cancer Ther., 4(2): 333–342.
Tian F, Zhang X W, Tong Y G, Yi Y H, Zhang S L, Li L, Sun P, Lin L P, Ding J. 2005. PE, a new sulfated saponin from sea cucumber, exhibits anti-angiogenic and anti-tumor activities in vitro and in vivo. Cancer Biol. Ther., 4(8):874–882.
Tosetti F, Ferrari N, De Flora S, Albini A. 2002. ’Angioprevention’: angiogenesis is a common and key target for cancer chemopreventive agents. FASEB J., 16(1): 2–14.
Wang Y J, Sun M, Zhang Y B, Hong Y G, Hao J H, Liu X P, Wang C B. 2000. Studies on preparation and characteristic of the marine low temperature lysozyme, Marine Fisheries Res., 21(4): 54–63.
Wang Z, Zheng L H, Yang S L, Niu R L, Chu E, Lin X K. 2007. N-acetylchitooligosaccharide is a potent angiogenic inhibitor both in vivo and in vitro. Biochem. Biophys. Res. Commun., 357(1): 26–31.
Willingham M C. 1999. Cytochemical methods for the detection of apoptosis. J. Histochem. Cytochem., 47(9): 1 101–1 110.
Yan C L, Ding B X, Lan X M, Guo S B, Xie Y Y, Wang C B. 2007. The toxicity study on marine low-temperature lysozyme. Food Chem. Toxicol., 46(2): 604–609.
Ye J L, Wang C B, Chen X H, Guo S B, Sun M. 2008. Marine lysozyme from a marine bacterium that inhibit angiogenesis and tumor growth. Appl. Microbiol. Biotechnol., 77(6): 1 261–1 267.
Yen W C, Prudente R Y, Corpuz M R, Negro-Vilar A, Lamph W W. 2006. A selective retinoid X receptor agonist bexarotene (LGD1069, targretin) inhibits angiogenesis and metastasis in solid tumours. Br. J. Cancer, 94(5):654–660.
Zhang J H, Xu M. 2000. DNA fragmentation in apoptosis. Cell Res., 10(3): 205–211.
Zou Y L, Sun M, Wang Y J. 2005. Purification and characterization of a lysozyme from a marine microorganism. Chin. J. Biotechnol., 21(3): 420–424.
0
Views
2
Downloads
4
CSCD
Publicity Resources
Related Articles
Related Author
Related Institution
京公网安备11010802024621