Levon M. Khachigian

ORCID: 0000-0003-3446-0323
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About
Contact & Profiles
Research Areas
  • Angiogenesis and VEGF in Cancer
  • RNA Interference and Gene Delivery
  • Advanced biosensing and bioanalysis techniques
  • Cell Adhesion Molecules Research
  • Coronary Interventions and Diagnostics
  • RNA modifications and cancer
  • RNA Research and Splicing
  • MicroRNA in disease regulation
  • Cytokine Signaling Pathways and Interactions
  • Signaling Pathways in Disease
  • Cancer-related molecular mechanisms research
  • NF-κB Signaling Pathways
  • Cardiac Ischemia and Reperfusion
  • Genomics and Chromatin Dynamics
  • Kruppel-like factors research
  • Platelet Disorders and Treatments
  • Atherosclerosis and Cardiovascular Diseases
  • Fibroblast Growth Factor Research
  • Nuclear Receptors and Signaling
  • Cardiac Fibrosis and Remodeling
  • Ubiquitin and proteasome pathways
  • Cancer-related gene regulation
  • Immunotherapy and Immune Responses
  • Proteoglycans and glycosaminoglycans research
  • RNA and protein synthesis mechanisms

UNSW Sydney
2016-2025

Tiande (China)
2018

Prince of Wales Hospital
2002-2014

The University of Sydney
2004-2013

Royal North Shore Hospital
2013

Skin Cancer Foundation
2012

Victor Chang Cardiac Research Institute
2012

Ross School
2012

Target (United States)
2012

The Heart Research Institute
2000-2010

Peter Arner Carsten O. Daub Kristoffer Vitting‐Seerup Robin Andersson Berit Lilje and 95 more Finn Drabløs Andreas Lennartsson Michelle Rönnerblad Olga Hrydziuszko Morana Vitezic Tom C. Freeman Ahmad M. N. Alhendi Peter Arner Richard A Axton J. Kenneth Baillie Anthony G Beckhouse Beatrice Bodega James Briggs Frank Brombacher Margaret R. Davis Michael Detmar Anna Ehrlund Mitsuhiro Endoh Afsaneh Eslami Michela Fagiolini Lynsey Fairbairn Geoffrey J. Faulkner Carmelo Ferrai Malcolm E Fisher Lesley M. Forrester Dan Goldowitz Reto Guler Thomas J Ha Mitsuko Hara Meenhard Herlyn Tomokatsu Ikawa Chieko Kai Hiroshi Kawamoto Levon M. Khachigian S. Peter Klinken Soichi Kojima Haruhiko Koseki Sarah Klein Niklas Mejhert Ken Miyaguchi Yosuke Mizuno Mitsuru Morimoto Kelly J Morris Christine L. Mummery Yutaka Nakachi Soichi Ogishima Mariko Okada Yasushi Okazaki Valerio Orlando Dmitry A. Ovchinnikov Robert Passier Margaret Patrikakis Ana Pombo Xian‐Yang Qin Sugata Roy Hiroki Sato Suzana Savvi Alka Saxena Anita Schwegmann Daisuke Sugiyama Rolf Swoboda Hiroshi Tanaka Andru Tomoiu Louise N Winteringham Ernst J. Wolvetang Chiyo Yanagi-Mizuochi Misako Yoneda Susan E. Zabierowski Peter Zhang Imad Abugessaisa Nicolas Bertin Alexander D. Diehl Shiro Fukuda Masaaki Furuno Jayson Harshbarger Akira Hasegawa Fumi Hori Sachi Ishikawa-Kato Yuri Ishizu Masayoshi Itoh Tsugumi Kawashima Miki Kojima Naoto Kondo Marina Lizio Terrence F. Meehan Chris Mungall Mitsuyoshi Murata Hiromi Nishiyori-Sueki Serkan Sahin Sayaka Nagao-Sato Jessica Severin Michiel de Hoon Jun Kawai Takeya Kasukawa Timo Lassmann

Although it is generally accepted that cellular differentiation requires changes to transcriptional networks, dynamic regulation of promoters and enhancers at specific sets genes has not been previously studied en masse. Exploiting the fact active are transcribed, we simultaneously measured their activity in 19 human 14 mouse time courses covering a wide range cell types biological stimuli. Enhancer RNAs, then messenger RNAs encoding transcription factors, dominated earliest responses....

10.1126/science.1259418 article EN Science 2015-02-13

A number of pathophysiologically relevant genes, including platelet-derived growth factor B-chain (PDGF-B), are induced in the vasculature after acute mechanical injury. In rat aorta, activated expression these genes was preceded by a marked increase amount early-growth-response gene product Egr-1 at endothelial wound edge. interacts with novel element proximal PDGF-B promoter, as well consensus elements promoters other This interaction is crucial for injury-induced promoter-dependent...

10.1126/science.271.5254.1427 article EN Science 1996-03-08
Shuhei Noguchi Takahiro Arakawa Shiro Fukuda Masaaki Furuno Akira Hasegawa and 95 more Fumi Hori Sachi Ishikawa-Kato Kaoru Kaida Ai Kaiho Mutsumi Kanamori-Katayama Tsugumi Kawashima Miki Kojima Atsutaka Kubosaki Ri-ichiroh Manabe Mitsuyoshi Murata Sayaka Nagao-Sato Kenichi Nakazato Noriko Ninomiya Hiromi Nishiyori-Sueki Shohei Noma Eri Saijyo Akiko Saka Mizuho Sakai Christophe Simon Naoko Suzuki Michihira Tagami Shoko Watanabe Shigehiro Yoshida Peter Arner Richard A Axton Magda Babina J. Kenneth Baillie Timothy C. Barnett Anthony G Beckhouse Antje Blumenthal Beatrice Bodega Alessandro Bonetti James Briggs Frank Brombacher Ailsa J Carlisle Hans Clevers Carrie Davis Michael Detmar Taeko Dohi Albert S.B. Edge Matthias Edinger Anna Ehrlund Karl Ekwall Mitsuhiro Endoh Hideki Enomoto Afsaneh Eslami Michela Fagiolini Lynsey Fairbairn Mary C. Farach‐Carson Geoffrey J. Faulkner Carmelo Ferrai Malcolm E Fisher Lesley M. Forrester Rie Fujita Jun-ichi Furusawa Teunis B. H. Geijtenbeek T Gingeras Dan Goldowitz Sven Guhl Reto Guler Stefano Gustincich Thomas J Ha Masahide Hamaguchi Mitsuko Hara Yuki Hasegawa Meenhard Herlyn Peter Heutink Kelly J Hitchens David Hume Tomokatsu Ikawa Yuri Ishizu Chieko Kai Hiroshi Kawamoto Yuki I. Kawamura Judith Kempfle Tony Kenna Juha Kere Levon M. Khachigian Toshio Kitamura Sarah Klein S. Peter Klinken Alan J. Knox Soichi Kojima Haruhiko Koseki Shigeo Koyasu Weon-Ju Lee Andreas Lennartsson Alan Mackay‐Sim Niklas Mejhert Yosuke Mizuno Hiromasa Morikawa Mitsuru Morimoto Kazuyo Moro Kelly J Morris Hozumi Motohashi

Abstract In the FANTOM5 project, transcription initiation events across human and mouse genomes were mapped at a single base-pair resolution their frequencies monitored by CAGE (Cap Analysis of Gene Expression) coupled with single-molecule sequencing. Approximately three thousands samples, consisting variety primary cells, tissues, cell lines, time series samples during activation development, subjected to uniform pipeline data production. The analysis started measuring RNA extracts assess...

10.1038/sdata.2017.112 article EN cc-by Scientific Data 2017-08-29

Hemodynamic forces, such as fluid shear stress, that act on the endothelial lining of cardiovascular system can modulate expression an expanding number genes crucial for homeostasis and pathogenesis vascular disease. A 6-bp core element (5'-GAGACC-3'), defined previously a shear-stress response is present in promoters many genes, including PDGF B-chain, whose modulated by stress. The identity nuclear protein(s) binding to this has not yet been elucidated. Using electrophoretic mobility shift...

10.1172/jci118106 article EN Journal of Clinical Investigation 1995-08-01

The platelet-derived growth factor (PDGF) A-chain has been implicated in the initiation and progression of vascular occlusive lesions. elements human PDGF-A promoter that mediate increased expression gene endothelial cells have not identified. A potent inducer is phorbol 12-myristate 13-acetate (PMA). 5′-Deletion transfection analysis revealed a G+C-rich region proximal required for PMA-inducible expression. This bears overlapping consensus recognition sequences Sp1 Egr-1. PMA induces Egr-1...

10.1074/jbc.270.46.27679 article EN cc-by Journal of Biological Chemistry 1995-11-01

Abstract Exposure of vascular endothelial cells to fluid mechanical forces can modulate the expression many genes involved in physiology and pathophysiology. Here, we report that platelet-derived growth factor (PDGF) A-chain gene is induced at level transcription cultured bovine aortic exposed a physiologic steady laminar shear stress (10 dyn/cm 2 ). 5′ Deletion analysis human PDGF-A promoter revealed GC-rich region near TATA box was required for shear-inducible reporter expression. This...

10.1161/01.atv.17.10.2280 article EN Arteriosclerosis Thrombosis and Vascular Biology 1997-10-01

Surface binding of galectin family members has the potential to link distinct glycan structures growth regulation. Therefore, we addressed antiproliferative galectin-1 (Gal-1) in a panel carcinoma cell lines. We discovered inhibition by Gal-1 epithelial tumor lines from different origins and provide evidence that this effect requires functional interaction with alpha5beta1 integrin. Antiproliferative effects result Ras-MEK-ERK pathway consecutive transcriptional induction p27. have further...

10.1074/jbc.m411580200 article EN cc-by Journal of Biological Chemistry 2005-08-17

10.1038/nprot.2006.393 article EN Nature Protocols 2006-12-01

Background: The basic region-leucine zipper protein c-Jun has been linked to cell proliferation, transformation, and apoptosis. However, a direct role for in angiogenesis not shown. Methods: We used human microvascular endothelial cells (HMEC-1) transfected with DNAzyme targeting the mRNA (Dz13), related oligonucleotides, or vehicle vitro models of migration, chemoinvasion, tubule formation, rat model corneal neovascularization, mouse solid tumor growth vascular factor (VEGF)–induced...

10.1093/jnci/djh120 article EN JNCI Journal of the National Cancer Institute 2004-05-04

Abstract Macrophage migration inhibitory factor (MIF) has been shown to promote leukocyte–endothelial cell interactions, although whether this occurs via an effect on endothelial function remains unclear. Therefore, the aims of study were examine ability MIF expressed by cells leukocyte adhesion and investigate exogenous interactions. Using small interfering RNA inhibit HUVEC production, we found that deficiency reduced TNF-stimulated HUVECs support rolling under flow conditions. These...

10.4049/jimmunol.0904104 article EN The Journal of Immunology 2010-06-17
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