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MYC oncogenes and human neoplastic disease
C E Nesbit1, J M Tersak, E V Prochownik
1Department of Pediatrics, Children's Hospital of Pittsburgh, Pennsylvania 15213, USA.
Oncogene
|June 23, 1999
Summary
The three MYC oncoproteins (c-MYC, N-MYC, and L-MYC) have distinct roles in human cancers. Deregulated expression of each MYC gene is linked to specific malignancies, highlighting their non-interchangeable functions in disease.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- The MYC family of oncoproteins, including c-MYC, N-MYC, and L-MYC, are implicated in the pathogenesis of numerous human cancers.
- Empirical evidence supports the significant role of MYC oncoproteins in the development and progression of various neoplastic diseases.
Purpose of the Study:
- To review and summarize the distinct in vivo roles of c-MYC, N-MYC, and L-MYC oncoproteins.
- To correlate the deregulated expression of specific MYC genes with particular human malignancies.
- To identify unresolved questions for future basic and clinical research regarding MYC gene involvement in cancer.
Main Methods:
- Review of data primarily from non-clinical studies on MYC oncoprotein function.
- Analysis of evidence linking specific MYC genes to distinct neoplastic diseases.
- Examination of studies utilizing primary tumor material to confirm MYC involvement.
Main Results:
- MYC oncoproteins (c-MYC, N-MYC, L-MYC) exhibit distinct functional roles in vivo.
- The deregulated expression of each MYC gene is specifically associated with certain human cancers.
- MYC genes are not interchangeable; their aberrant functional consequences differ.
Conclusions:
- The distinct roles of MYC oncoproteins explain their specific associations with different human malignancies.
- Further investigation is warranted to address unresolved questions regarding MYC gene involvement in cancer causation and progression.
- Confirmatory evidence from primary tumor studies supports the role of MYC members in specific cancers.