M. Trovato et al., Expression of CD30 ligand and CD30 receptor in normal thyroid and benign and malignant thyroid nodules, THYROID, 11(7), 2001, pp. 621-628
Because the CD30 ligand (CD30L)/CD30 receptor (CD30) system is expressed in
certain malignancies, but has not been studied in thyroid nodules, we inve
stigated its immunohistochemical expression in 6 normal thyroids (NT) and 1
31 thyroid nodules: 28 colloid nodules (CN), 45 adenomas (15 oncocytic [OA]
, 30 follicular [FA]) and 58 carcinomas (15 follicular [FTC], 1 insular [IT
C], 6 anaplastic [ATC], 30 papillary [PTC], and 6 medullary [MTC]). NT and
CN expressed neither CD30L nor CD30 (CD30L(-)/CD30(-)). Forty percent of OA
and 20% of FA showed epithelial coexpression of CD30L and CD30, and inters
titial expression of CD30L, which was also observed in the surrounding norm
al tissue. Within malignancies, epithelial coexpression of CD30L and CD30 w
as observed in 7% of FTC, 33% of ATC, 67% of PTC, and 67% of MTC. Only PTC
and MTC showed epithelial expression of CD30L in the perinodular tissue wit
h similar frequency (80% PTC, 75% MTC). PTC and MTC had the highest proport
ion of CD30L(+) or CD30(+) cells, and together with OA, a thus far unreport
ed nuclear location of CD30L. In PTC, the proportion of CD30L(+) cells and
the prevalence of nuclear location of CD30L correlated inversely and direct
ly, respectively, with aggressiveness. Ln conclusion, CD30L/CD30 signaling
is activated only past the colloid nodule stage, most frequently in an auto
crine fashion.