HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Multifunction protein staphylococcal nuclease domain containing 1 (SND1) promotes tumor angiogenesis in human hepatocellular carcinoma through novel pathway that involves nuclear factor κB and miR-221.

Abstract
Staphylococcal nuclease domain-containing 1 (SND1) is a multifunctional protein that is overexpressed in multiple cancers, including hepatocellular carcinoma (HCC). Stable overexpression of SND1 in Hep3B cells expressing a low level of SND1 augments, whereas stable knockdown of SND1 in QGY-7703 cells expressing a high level of SND1 inhibits establishment of xenografts in nude mice, indicating that SND1 promotes an aggressive tumorigenic phenotype. In this study we analyzed the role of SND1 in regulating tumor angiogenesis, a hallmark of cancer. Conditioned medium from Hep3B-SND1 cells stably overexpressing SND1 augmented, whereas that from QGY-SND1si cells stably overexpressing SND1 siRNA significantly inhibited angiogenesis, as analyzed by a chicken chorioallantoic membrane assay and a human umbilical vein endothelial cell differentiation assay. We unraveled a linear pathway in which SND1-induced activation of NF-κB resulted in induction of miR-221 and subsequent induction of angiogenic factors Angiogenin and CXCL16. Inhibition of either of these components resulted in significant inhibition of SND1-induced angiogenesis, thus highlighting the importance of this molecular cascade in regulating SND1 function. Because SND1 regulates NF-κB and miR-221, two important determinants of HCC controlling the aggressive phenotype, SND1 inhibition might be an effective strategy to counteract this fatal malady.
AuthorsPrasanna Kumar Santhekadur, Swadesh K Das, Rachel Gredler, Dong Chen, Jyoti Srivastava, Chadia Robertson, Albert S Baldwin Jr, Paul B Fisher, Devanand Sarkar
JournalThe Journal of biological chemistry (J Biol Chem) Vol. 287 Issue 17 Pg. 13952-8 (Apr 20 2012) ISSN: 1083-351X [Electronic] United States
PMID22396537 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • CXCL16 protein, human
  • Chemokine CXCL16
  • Chemokines, CXC
  • MIRN221 microRNA, human
  • MicroRNAs
  • NF-kappa B
  • Nuclear Proteins
  • RNA, Small Interfering
  • Receptors, Scavenger
  • Endonucleases
  • SND1 protein, human
  • angiogenin
  • Ribonuclease, Pancreatic
Topics
  • Carcinoma, Hepatocellular (metabolism)
  • Cell Nucleus (metabolism)
  • Chemokine CXCL16
  • Chemokines, CXC (biosynthesis)
  • Endonucleases
  • Enzyme-Linked Immunosorbent Assay (methods)
  • Gene Expression Regulation, Neoplastic
  • Human Umbilical Vein Endothelial Cells (metabolism)
  • Humans
  • Liver Neoplasms (metabolism)
  • MicroRNAs (metabolism)
  • NF-kappa B (metabolism)
  • Neoplasm Metastasis
  • Neovascularization, Pathologic
  • Nuclear Proteins (metabolism)
  • RNA, Small Interfering (metabolism)
  • Receptors, Scavenger (biosynthesis)
  • Ribonuclease, Pancreatic (biosynthesis)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: