Fiche publication
Date publication
novembre 1995
Journal
Cellular and molecular biology (Noisy-le-Grand, France)
Auteurs
Membres identifiés du Cancéropôle Est :
Pr MERLIN Jean-Louis
Tous les auteurs :
Edorh A, Parache RM, N'Sossani B, Bottin MC, Merlin JL, Colosetti P, Guillemin F, Le Faou A, Rihn B
Lien Pubmed
Résumé
A quantitative method of polymerase chain reaction (PCR) using both digoxigenin and radioactive labelled probes has been used for the detection of the c-erbB-2 proto-oncogene amplification in breast carcinomas with formalin-fixed paraffin-embedded tissue sections. c-erbB-2 proto-oncogene amplification has been demonstrated in 14 infiltrating ductal carcinomas. The technique consisted of the co-amplification of c-erbB-2 and IFN-gamma (interferon-gamma) genes. The latter was considered as a single copy gene per genome-equivalent. The aim of this study was to compare two quantitative PCR techniques based on the incorporation of either digoxigenin-11-dUTP or 32P-dCTP, during amplification. For the colorigenic method, using the Dig system, after electrophoresis and transfer, the specific bands were revealed with a chromogenic substrate of phosphatase. Their intensity estimated by scanning photometry following blot transparisation. After electrophoresis, the radioactive gel was submitted to radioautography and the band intensities evaluated by scanning spectrophotometry. For the 14 samples, a good agreement between both methods was noted. The colorigenic method is a valuable alternative to radiolabelling due to: i) time saving, ii) reagent conservation, iii) safe manipulation and iv) sensitivity of the same order for both methods.
Mots clés
Base Sequence, Breast Neoplasms, genetics, Carcinoma, Ductal, Breast, genetics, Colorimetry, DNA Primers, genetics, DNA, Neoplasm, genetics, Digoxigenin, Evaluation Studies as Topic, Female, Gene Amplification, Genes, erbB-2, Humans, Interferon-gamma, genetics, Molecular Probes, Molecular Sequence Data, Phosphorus Radioisotopes, Polymerase Chain Reaction, methods
Référence
Cell. Mol. Biol. (Noisy-le-grand). 1995 Nov;41(7):967-73
