C-KIT PROTOONCOGENE IS MORE LIKELY TO LOSE EXPRESSION IN DIFFERENTIATED THYROID-CARCINOMA THAN 3 THYROID-SPECIFIC GENES - THYROID PEROXIDASE, THYROGLOBULIN, AND THYROID-STIMULATING HORMONE-RECEPTOR
T. Tanaka et al., C-KIT PROTOONCOGENE IS MORE LIKELY TO LOSE EXPRESSION IN DIFFERENTIATED THYROID-CARCINOMA THAN 3 THYROID-SPECIFIC GENES - THYROID PEROXIDASE, THYROGLOBULIN, AND THYROID-STIMULATING HORMONE-RECEPTOR, Endocrine journal, 42(5), 1995, pp. 723-728
Although c-kit proto-oncogene product is known to be weakly expressed
on normal thyrocytes, its function is unclear. In order to investigate
the significance of thyroid c-kit, c-kit gene expression in 37 variou
s thyroid tissues was analyzed by comparing c-kit gene expression with
the mRNA expression of three thyroid-specific genes: thyroid peroxida
se, thyroglobulin, and thyroid stimulating hormone receptor. c-kit mRN
A was hardly detected by the usual northern blot method in 2 of 7 foll
icular carcinomas, 11 of 12 papillary carcinomas, and a medullary carc
inoma. On the other hand, a high level of c-kit mRNA expression was fo
und in all 17 benign thyroid tissues (4 normal thyroid tissues, 4 Grav
es' disease, 2 adenomatous goiters, and 7 follicular adenomas). This s
tudy found that c-kif proto-oncogene is more likely to lose expression
in differentiated thyroid carcinoma than any thyroid-specific gene. D
ecreased c-kit gene expression may serve as an indicator for the de-di
fferentiation of thyrocytes.