Ch. Lee et al., HIGH-FREQUENCY OF REARRANGEMENT OF THE RET PROTOONCOGENE (RET PTC) INCHINESE PAPILLARY THYROID CARCINOMAS/, The Journal of clinical endocrinology and metabolism, 83(5), 1998, pp. 1629-1632
The activation of RET protooncogene, through chromosomal translocation
, is unique to papillary thyroid carcinomas. Rearrangement of the RET
kinase domain to 3 partner genes has been described, of which the RET/
PTC1 is the most common. To investigate the frequency of RET rearrange
ment in Chinese papillary thyroid carcinomas, we have performed RT-PCR
to amplify specific RET/PTC transcripts. Among the papillary thyroid
carcinomas of 11 patients examined, we have identified 2 containing RE
T/PTC1, 3 containing RET/PTC2, and 1 containing RET/PTC3 oncogenes. Al
though the cause of the high frequency of RET/PTC oncogenes in Chinese
papillary thyroid carcinomas is unknown, our study suggests that RET
rearrangement is an important genetic lesion underlying the developmen
t of thyroid papillary carcinoma in Taiwan.