Genetic and genomic analysis modeling of germline c-MYC overexpression and cancer susceptibility
2008

Genetic Analysis of c-MYC Overexpression and Cancer Risk

Sample size: 54 publication Evidence: moderate

Author Information

Author(s): Solé Xavier, Hernández Pilar, de Heredia Miguel López, Armengol Lluís, Rodríguez-Santiago Benjamín, Gómez Laia, Maxwell Christopher A, Aguiló Fernando, Condom Enric, Abril Jesús, Pérez-Jurado Luis, Estivill Xavier, Nunes Virginia, Capellá Gabriel, Gruber Stephen B, Moreno Víctor, Pujana Miguel Angel

Primary Institution: Catalan Institute of Oncology, IDIBELL, L'Hospitalet, Barcelona, Spain

Hypothesis

Variation at 8q24 cis-regulator(s) of transcription can significantly alter germline c-MYC expression levels and contribute to cancer susceptibility.

Conclusion

The study suggests that germline c-MYC overexpression may promote prostate cancer susceptibility by down-regulating the tumor suppressor KLF6 gene.

Supporting Evidence

  • Genetic variation at 8q24 has been associated with prostate cancer risk.
  • c-MYC overexpression correlates with more aggressive forms of prostate cancer.
  • Significant SNPs were identified that associate with c-MYC expression levels.

Takeaway

This study found that changes in a specific gene can make people more likely to get prostate cancer by affecting another important gene that helps prevent cancer.

Methodology

The study used genetic association scans and expression profiling in normal prostate tissues to analyze c-MYC expression and its association with prostate cancer risk.

Limitations

The genetic scanning analysis is susceptible to false positives, and larger sample sizes are needed for definitive conclusions.

Participant Demographics

The study included individuals of European ancestry and African Americans.

Statistical Information

P-Value

0.004

Confidence Interval

0.06 – 0.41

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/1471-2164-9-12

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