Anderson M, Muro-Cacho C, Cordero J, Livingston S, Muñoz-Antonia T
Molecular Oncology Program, University of South Florida College of Medicine, Tampa, USA.
Arch Otolaryngol Head Neck Surg. 1999 Aug;125(8):849-54. doi: 10.1001/archotol.125.8.849.
To study the intracellular location of transforming growth factor beta type II receptors (TbetaR-II) in verrucous carcinoma (VC) and squamous cell carcinoma (SqCC), and to evaluate their role in the biological behavior of both neoplasias.
Ten VC and 10 well-differentiated SqCC specimens were analyzed by immunohistochemistry and in situ hybridization for the expression and intracellular location of TbetaR-II. Receptor expression was evaluated in areas of invasion and in areas of transformation of VC into SqCC. TbetaR-II expression was compared with expression of the type I receptor (TbetaR-I).
Formalin-fixed, paraffin-embedded tissue sections from VCs and well-differentiated SqCCs, operated on at the H. L. Moffitt Cancer Center and Research Institute from May 1987 to January 1998, were selected for the study.
None.
While in all VCs TbetaR-II was found to be located along the membrane of the neoplastic keratinocytes, TbetaR-II expression in SqCC was observed predominantly in a cytoplasmic location. This cytoplasmic location of TbetaR-II was also seen in areas of transition from VC to SqCC. Expression of TbetaR-I was found in a cytoplasmic location in both tumor types.
The membranous location of TbetaR-II in VC exposes the receptor to the growth inhibitory control of TGF-beta and may explain why VC tumors are less aggressive clinically. The marked reduction of membranous TbetaR-II and their predominant cytoplasmic location diminishes TGF-beta growth inhibition and may contribute to the transformation of VC into the more aggressive SqCC.
研究II型转化生长因子β受体(TbetaR-II)在疣状癌(VC)和鳞状细胞癌(SqCC)中的细胞内定位,并评估其在这两种肿瘤生物学行为中的作用。
采用免疫组织化学和原位杂交技术分析10例VC和10例高分化SqCC标本中TbetaR-II的表达及细胞内定位。在VC的侵袭区域和VC向SqCC转化的区域评估受体表达情况。将TbetaR-II的表达与I型受体(TbetaR-I)的表达进行比较。
选取1987年5月至1998年1月在H. L. Moffitt癌症中心和研究所接受手术的VC和高分化SqCC的福尔马林固定、石蜡包埋组织切片进行研究。
无。
在所有VC中,TbetaR-II定位于肿瘤角质形成细胞的细胞膜上,而在SqCC中,TbetaR-II的表达主要位于细胞质中。在从VC向SqCC转变的区域也可见到TbetaR-II的这种细胞质定位。在两种肿瘤类型中,TbetaR-I的表达均位于细胞质中。
VC中TbetaR-II的膜定位使该受体受到TGF-β的生长抑制控制,这可能解释了为什么VC肿瘤在临床上侵袭性较小。膜性TbetaR-II的显著减少及其主要的细胞质定位削弱了TGF-β的生长抑制作用,可能促使VC转变为侵袭性更强的SqCC。