Combined use of expression and CGH arrays pinpoints novel candidate genes in Ewing sarcoma family of tumors
2009

Identifying Genes in Ewing Sarcoma

Sample size: 31 publication Evidence: moderate

Author Information

Author(s): Suvi Savola, Arto Klami, Abhishek Tripathi, Tarja Niini, Massimo Serra, Piero Picci, Samuel Kaski, Diana Zambelli, Katia Scotlandi, Sakari Knuutila

Primary Institution: University of Helsinki

Hypothesis

The study aims to pinpoint genomic regions and potential target genes involved in the tumorigenesis of Ewing sarcoma family of tumors (ESFT).

Conclusion

Array CGH and integration analysis proved effective in identifying chromosome regions and novel target genes involved in the tumorigenesis of ESFT.

Supporting Evidence

  • 87% of the cases showed copy number changes.
  • Patients with three or fewer copy number changes had significantly better survival rates.
  • 20 novel ESFT associated putative oncogenes and tumor suppressor genes were identified.

Takeaway

Researchers looked at tumor samples from kids with a type of bone cancer to find important genes that might help us understand how the cancer grows.

Methodology

The study used array comparative genomic hybridization (CGH) and expression arrays to analyze copy number alterations and gene expression in ESFT patient samples.

Limitations

The sample size was not large enough to draw definitive conclusions about the prognostic value of HDGF expression.

Participant Demographics

The mean age of patients was 20.7 years, with a male-to-female ratio of 22:9.

Statistical Information

P-Value

0.03

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/1471-2407-9-17

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication