Association of RET codon 691 polymorphism in radiation-induced human thyroid tumours with C-cell hyperplasia in peritumoural tissue
2002

RET Gene Polymorphism and C-cell Hyperplasia in Thyroid Tumors

Sample size: 29 publication 10 minutes Evidence: high

Author Information

Author(s): Bounacer A, Du Villard J A, Wicker R, Caillou B, Schlumberger M, Sarasin A, Suárez H G

Primary Institution: Institut de Recherches sur le Cancer, C.N.R.S.

Hypothesis

Is there a relationship between RET gene polymorphism and C-cell hyperplasia in thyroid tumors associated with radiation exposure?

Conclusion

The study found a significantly higher frequency of C-cell hyperplasia in peritumoral thyroid tissues of radiation-induced epithelial thyroid tumors compared to sporadic tumors and normal tissues.

Supporting Evidence

  • 55% of radiation-induced thyroid tumors had C-cell hyperplasia.
  • Only 7% of sporadic thyroid tumors showed C-cell hyperplasia.
  • The RET G691S polymorphism was found in 88% of tumors with C-cell hyperplasia.

Takeaway

The study shows that people who had radiation exposure and developed thyroid tumors are more likely to have a specific genetic change and a condition called C-cell hyperplasia in the surrounding tissue.

Methodology

The study analyzed thyroid tissues from patients with radiation-induced tumors and compared them to sporadic tumors and normal tissues for genetic alterations and C-cell hyperplasia.

Limitations

The study did not explore the exact molecular mechanisms linking the RET polymorphism to C-cell hyperplasia.

Participant Demographics

The study included 29 patients (18 women, 11 men) with a mean age of 29.8 years at diagnosis.

Statistical Information

P-Value

0.0001

Statistical Significance

p=0.0001

Digital Object Identifier (DOI)

10.1038/sj.bjc.6600371

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