MYCN gene amplification in rhabdomyosarcoma
D Driman, PS Thorner, ML Greenberg… - Cancer, 1994 - Wiley Online Library
D Driman, PS Thorner, ML Greenberg, S Chilton‐MacNeill, J Squire
Cancer, 1994•Wiley Online LibraryBackground. Amplification of the MYCN oncogene, formerly known as N‐myc, has been
seen in several malignant tumors, particularly neuroblastoma, where its association with a
poor clinical outcome is the clearest example of a clinically relevant oncogene mutation in
any human cancer. Methods. The incidence and clinical significance of MYCN amplification
in rhabdomyosarcoma (RMS) was assessed by Southern blot analysis in this retrospective
study of seven alveolar RMS and six embryonal RMS. Results. MYCN amplification (4‐to 13 …
seen in several malignant tumors, particularly neuroblastoma, where its association with a
poor clinical outcome is the clearest example of a clinically relevant oncogene mutation in
any human cancer. Methods. The incidence and clinical significance of MYCN amplification
in rhabdomyosarcoma (RMS) was assessed by Southern blot analysis in this retrospective
study of seven alveolar RMS and six embryonal RMS. Results. MYCN amplification (4‐to 13 …
Abstract
Background. Amplification of the MYCN oncogene, formerly known as N‐myc, has been seen in several malignant tumors, particularly neuroblastoma, where its association with a poor clinical outcome is the clearest example of a clinically relevant oncogene mutation in any human cancer.
Methods. The incidence and clinical significance of MYCN amplification in rhabdomyosarcoma (RMS) was assessed by Southern blot analysis in this retrospective study of seven alveolar RMS and six embryonal RMS.
Results. MYCN amplification (4‐ to 13‐fold) was present in three of seven alveolar RMS (42.9%) but in none of the embryonal RMS. There was no significant difference between the clinical behavior of the MYCN‐amplified and unamplified tumors, and no correlation was found with the light microscopic appearances of the tumors or with desmin immunoreactivity.
Conclusions. The findings are compatible with previous studies that demonstrated cytogenetic evidence of gene amplification in RMS, and help to clarify conflicting reports in the literature about MYCN amplification in alveolar and embryonal RMS. The results raise the possibility of important biologic differences between these subtypes of RMS, differences that warrant further investigation.
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