Michel Rigaud

Prof. Dr. Michel Rigaud


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 April 2015 in Clinical and Translational Medicine
Verified
Journal Article
Open access
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GBGuislaine Barriere
Guislaine Barriere
PFPietro Fici
Pietro Fici
Giulia GalleraniGiulia Gallerani
Giulia Gallerani
FFFrancesco Fabbri
Francesco Fabbri
MRMichel Rigaud
Michel Rigaud
Epithelial mesenchymal transition (EMT) is a physiological process necessary to normal embryologic development. However in genesis of pathological situations, this transition can be perverted and signaling pathways have different regulations from those of normal physiology. In cancer invasion, such a mechanism leads to generation of circulating tumor cells. Epithelial cancer cells become motile mesenchymal cells able to shed from the primary tumor and enter in the blood circulation. This is the major part of the invasive way of cancer. EMT is also implicated in chronic diseases like fibrosis and particularly renal fibrosis. In adult organisms, healing is based on EMT which is beneficial to repair wounds even if it can sometimes exceed its goal and elicit fibrosis. In this review, we delineate the clinical significance of EMT in both physiological and pathological circumstances.

23 March 2012 in BMC Cancer
Verified
Journal Article
Open access
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GBGuislaine Barrière
Guislaine Barrière
ARAlain Riouallon
Alain Riouallon
JRJoël Renaudie
Joël Renaudie
MTMichel Tartary
Michel Tartary
MRMichel Rigaud
Michel Rigaud
Background: Epithelial mesenchymal transition (EMT) is a crucial event likely involved in dissemination of epithelial cancer cells. This process enables them to acquire migratory/invasive properties, contributing to tumor and metastatic spread. To know if this event is an early one in breast cancer, we developed a clinical trial. The aim of this protocol was to detect circulating tumor cells endowed with mesenchymal and/or stemness characteristics, at the time of initial diagnosis. Breast cancer patients (n = 61), without visceral or bone metastasis were enrolled and analysis of these dedifferentiated circulating tumor cells (ddCTC) was realized. Methods: AdnaGen method was used for enrichment cell selection. Then, ddCTC were characterized by RT-PCR study of the following genes: PI3Kα, Akt-2, Twist1 (EMT markers) and ALDH1, Bmi1 and CD44 (stemness indicators). Results: Among the studied primary breast cancer cohort, presence of ddCTC was detected in 39% of cases. This positivity is independant from tumor clinicopathological factors apart from the lymph node status. Conclusions: Our data uniquely demonstrated that in vivo EMT occurs in the primary tumors and is associated with an enhanced ability of tumor cells to intravasate in the early phase of cancer disease. These results suggest that analysis of circulating tumor cells focused on cells showing mesenchymal or stemness characteristics might facilitate assessment of new drugs in clinical trials.

1 July 2013
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Journal Article
Open access
PDF file
GBGuislaine Barriere
Guislaine Barriere
MRMichel Rigaud
Michel Rigaud
After clouds sun again shines on circulating tumor cells research