Reduced risk of synovial sarcoma in females: X-chromosome inactivation?
2002

Reduced Risk of Synovial Sarcoma in Females

Sample size: 680 publication Evidence: moderate

Author Information

Author(s): Bu X, Bernstein L, Brynes R K

Primary Institution: University of Southern California, Keck School of Medicine

Hypothesis

We hypothesize that X-chromosome inactivation reduces the likelihood of synovial sarcoma development in females.

Conclusion

The study provides evidence that X-inactivation may explain the similar risk of synovial sarcoma in females compared to males.

Supporting Evidence

  • The incidence of synovial sarcoma is roughly one per million adults.
  • More than 95% of synovial sarcoma cases demonstrate a characteristic t(X;18) translocation.
  • The male-to-female ratio of age-standardised incidence rates is 1.1:1.
  • The observed proportion of male cases was 53.3%, which aligns with the hypothesis of X-inactivation.

Takeaway

This study suggests that girls and women are less likely to get a certain type of cancer because one of their X-chromosomes is turned off.

Methodology

The study analyzed age-specific and sex-specific incidence data from the SEER program for 680 cases of synovial sarcoma.

Potential Biases

The study acknowledges potential ascertainment bias from non-population-based case series.

Limitations

The study did not analyze data according to race or geographical region due to limited case numbers.

Participant Demographics

Data derived from SEER registries, representing about 14% of the US population.

Statistical Information

P-Value

p<0.00001

Statistical Significance

p<0.00001

Digital Object Identifier (DOI)

10.1038/sj.bjc.6600362

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