GIGA-Cancer

The GIGA-Cancer unit is composed of several laboratories sharing a common interest in the study of the mechanisms involved during cancer development and progression. More particularly, GIGA-Cancer researchers investigate the molecular mechanisms implicated during tumor invasion and metastases through the study of several protease families (metalloproteases, ADAMTs,...) that degrade the extracellular matrix. They also examine the role of several extracellular matrix components such as the SIBLINGs (Small integrin-binding ligand N-linked proteins) during the several steps of cancer progression.

GIGA-CANCER groups also have a special interest in the study of angiogenesis, a key biological process that allows the neovascularization of malignant lesions, enabling their local growth and facilitating the dissemination of cancer cells. Finally, GIGA-Cancer is involved in projects aiming to identify new accessible cancer biomarkers which could be the bases for targeted cancer therapies.

NoelA 

Head of the thematic research unit
Agnès Noël

 


Research projects

 

Research units

Tumour and development biology See more
   Jean-Michel Foidart, Agnès Noël

Metastases Research See more
    Vincent Castronovo, Akeila Bellahcene

Pathology
    Jacques Boniver, Philippe Delvenne

Molecular biology & genetic engineering See more
    Joseph Martial, Ingrid Struman

Laboratory of connective tissues biology See more
   Alain Colige

Histology - Cytology
    Marie-Paule Defresne

Human genetics See more
    Vincent Bours

   Laboratory of cellular and molecular epigenetics See more
   Luc Willems

 Advisory Board

  • Jacques Ghysdael, Institut Curie Paris, France
  • Yvan de Launoit, Institut Pasteur, Lille, France
  • Giulia Taraboletti, Mario Negri Institute for pharmacological Research, Bergamo, Italy
  • Pascal Barbry, CNRS, Sophia Antipolis, France

Significant publications

Paupert J, Sounni NE, Noel A.
Lymphangiogenesis in post-natal tissue remodeling: Lymphatic endothelial cell connection with its environment.
Mol Aspects Med. 2011;32:146-158 

Pirotte S, Lamour V, Lambert V, Alvarez Gonzalez ML, Ormenese S, Noël A, Mottet D, Castronovo V, Bellahcène A.
Dentin matrix protein 1 induces membrane expression of VE-cadherin on endothelial cells and inhibits VEGF-induced angiogenesis by blocking VEGFR-2 phosphorylation.
Blood. 2011 Feb 24;117(8):2515-26 

Lecomte J, Louis K, Detry B, Blacher S, Lambert V, Bekaert S, Munaut C, Paupert J, Blaise P, Foidart JM, Rakic JM, Krane SM, Noel A.
Bone marrow-derived mesenchymal cells and mmp13 contribute to experimental choroidal neovascularization.
Cell Mol Life Sci. 2011;68:677-686 See more

El Hour M, Moncada-Pazos A, Blacher S, Masset A, Cal S, Berndt S, Detilleux J, Host L, Obaya AJ, Maillard C, Foidart JM, Ectors F, Noel A, Lopez-Otin C.
Higher sensitivity of Adamts12-deficient mice to tumor growth and angiogenesis.
Oncogene 29(20): 3025-32 (2010) See more.

Bellahcène A, Castronovo V, Ogbureke KU, Fisher LW, Fedarko NS.
Small integrin-binding ligand N-linked glycoproteins (SIBLINGs): multifunctional proteins in cancer.
Nat Rev Cancer. 2008 Mar;8(3):212-26. Review.

Bruyère F, Melen-Lamalle L, Blacher S, Roland G, Thiry M, Moons L, Frankenne F, Carmeliet P, Alitalo K, Libert C, Sleeman JP, Foidart JM, Noël A.
Modeling lymphangiogenesis in a three-dimensional culture system.
Nat Methods. 2008; 5(5):431-7.

Herens C, Lambert F, Quintanilla-Martinez L, Bisig B, Deusings C, de Leval L.
Cyclin D1-negative mantle cell lymphoma with cryptic t(12;14)(p13;q32) and cyclin D2 overexpression.
Blood, 2008, 111 : 1745-46.

Kesteloot F, Desmoulière A, Leclercq I, Thiry M, Arrese JE, Prockop DJ, Lapière CM, Nusgens BV, Colige A.
ADAM metallopeptidase with thrombospondin type 1 motif 2 inactivation reduces the extent and stability of carbon tetrachloride-induced hepatic fibrosis in mice.
Hepatology. 2007 Nov;46(5):1620-31.

Mineur P, Colige AC, Deroanne CF, Dubail J, Kesteloot F, Habraken Y, Noël A, Vöö S, Waltenberger J, Lapière CM, Nusgens BV, Lambert CA.
Newly identified biologically active and proteolysis-resistant VEGF-A isoform VEGF111 is induced by genotoxic agents.
The Journal of Cell Biology, 2007, 179,6;1261-1273.


See all the GIGA publications