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Icahn Medical Institute Floor 14 Room Lab 14-26
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212-659-6771

Olga Camacho-Vanegas

ASSISTANT PROFESSOR  Genetics and Genomic Sciences

Overview

Gender Female
E-mail olga.camacho@mssm.edu
Education and Training PhD, University of Rome

Olga Camacho-Vanegas, Ph.D.
Assistant Professor
Department of Genetics and Genomic Sciences
The Mount Sinai School of Medicine
1425 Madison Avenue , Room 14-26D
New York, New York 10029-6574
Phone: 212-241-6771
Fax: 212-241-5703
E-mail: olga.camacho@mssm.edu

Training

Education and Training PhD, University of Rome

Research

Our Laboratory involve in a number of translational research projects. In particular we are focused on human gene discovery projects with a particular interest in tumor suppressor genes, the generation of animal model for understanding the biological role of these genes in cancer and ultimately the generation of novel therapeutic targets to cure cancer.

Among the projects running in our laboratory, I am leading the project: Linkage analysis and gene descovery for a novel bone dysplasia/cancer syndrome linked to chromosome 9p21-22:DMS-MFH (Diaphyseal medullary stenosis (sclerosis) with bone malignancy (malignant fibrous histiocytoma): Hardcastle syndrome, Malignant fibromatosis)". Throught linkage analysis, we have narrow the disease region to 1.6 Mb and have a identified a very interesting candidate gene.  At present, we are in the process to demostrate the discovery a "new tumor suppressor gene". The use of  in vivo and in vitro experimental strategies will help us to establish the function of the novel gene and to define the underlying disease mechanisms.

Another project in which I am actively participating is aimed to define the role and the molecular mechanisms by which of the Kruppel-like factor (KLF6) tumor suppressor gene and its KLF6-SV1 splice variant  in human cancer.


Publications

Difeo A, Narla G, Camacho-Vanegas O, Nishio H, Martignetti JA, Buller RE, Friedman SL, Walsh MJ, Rose SL. E-cadherin is a novel transcriptional target of the KLF6 tumor suppressor. Oncogene 2006 May 15;.


DiFeo A, Narla G, Hirshfeld J, Camacho-Vanegas O, Narla J, Rose SL, Martignetti JA, Yao S, Levine A, Birrer MJ, Bonome T, Friedman SL, Buller RE, Kalir T. Roles of KLF6 and KLF6-SV1 in ovarian cancer progression and intraperitoneal dissemination. Clin Cancer Res 2006; 12: 3730-3739.


Goutham N, Difeo A, Yao S, Banno A, Hod E, Reeves HL, Martignetti J, Camacho-Vanegas O, Levine A, Kirschenbaum A, Chan AM, Friedman SL, Qiao RF. Targeted inhibition of the KLF6 splice variant, KLF6 SV1, supresses prostate cancer cell growth and spread. Cancer Research 2005; 65: 5761-5768.


Lucioli S, Pepe G, Mercuri E, Camacho-Vanegas O, Lucarini L, Pietroni V, Urtizberea A, Ben Yaou R, De Visser M, Bonnemann C, Lannaccone ST, Merlini L, Bushby K, Muntoni F, Bertini E, Chu ML, Giusti B. Detection of common and private mutations in the COL6A1 gene of Bethlem myopathy patients. Neurology 2005; 64: 1931-1937.


Vanegas OC, Zhang RZ, Sabatelli P, Lattanzi G, Pepe G, Guisti B, Columbaro M, Chu ML, Merlini L, Bencivenga P. Novel COL6A1 splicing mutation in a family affected by mild Bethlem myopathy. Muscle Nerve 2002; 25: 513-519.


Longo L, Vanegas OC, Patel M, Rosti V, Li H, ande Luzzato L, Merghoub T, Pandolfi PP, Notaro R, Manova K, Waka J. Maternally transmitted severe glucose 6-phospate dehydrogenase deficiency is an embryonic lethal. EMBO J 2002; 21: 4229-4239.


Camacho-Vanegas O, Bertini E, Zhang RZ, Petrini S, Pepe G, Sabatelli P, Giusti B, Chu ML, Minosse C. Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VI. Proc. Natl. Acad. Sci. USA 2001; 98: 7516-7521.


Rovira A, De Angioletti M, Camacho-Vanegas O, Liu D, Luzzatto L, Gallartdo HF, Notaro R, Sadelain R, Rosti V. Stable in vivo expression of glucose-6-phosphate dehydrogenase (G6PD) and rescue of G6PD deficiency in stem cells by gene transfer. Blood 2000; 96: 411-417.


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