Roh Joo-Young, Kee Sun-Ho, Choi Jung-Woo, Lee Ji-Hye, Lee Ju-Han, Lee Eung Seok, Kim Young-Sik
Department of Dermatology, Gachon Medical School, Gil Medical Center, Incheon, Korea.
J Cutan Pathol. 2007 Feb;34(2):166-73. doi: 10.1111/j.1600-0560.2006.00583.x.
Different combinations of beta-tubulin isotypes contribute to the diverse functions of microtubules (MTs). Class II beta-tubulin (class II tubulin) is up-regulated in differentiated keratinocytes. In contrast, the expression of class II tubulin in follicular differentiation and cutaneous tumors has not been studied.
The immunohistochemical expression of class II tubulin was investigated in 117 cutaneous tumors: 30 squamous cell carcinomas (SCCs), seven keratoacanthomas (KAs), 57 basal cell carcinomas (BCCs), 23 trichoepitheliomas (TEs), and in the adjacent non-neoplastic skin.
Class II tubulin was expressed in the keratinocytes of the granular layer, melanocytes, hair cortical and cuticular cells, inner root sheath (IRS), companion layer (CL) of the outer root sheath (ORS), and mesenchymal cells with Schwannian or myogenic differentiation. Moreover, class II tubulin expression was increased in the areas of squamous or follicular differentiation in cutaneous tumors. On grading the follicular differentiation or myofibroblastic response with anti-class II tubulin, TE showed follicular differentiation more frequently (p < 0.001) with less of a myofibroblastic response (p = 0.001) than BCC.
Class II tubulin expression is closely related to squamous or follicular differentiation and may be helpful in distinguishing most SCCs from KAs and BCC from TE. However, it does not reliably distinguish well-differentiated, crateriform SCC from KA.
β-微管蛋白异构体的不同组合促成了微管(MTs)的多种功能。II类β-微管蛋白(II类微管蛋白)在分化的角质形成细胞中上调。相比之下,II类微管蛋白在毛囊分化和皮肤肿瘤中的表达尚未得到研究。
研究了117例皮肤肿瘤中II类微管蛋白的免疫组化表达:30例鳞状细胞癌(SCC)、7例角化棘皮瘤(KA)、57例基底细胞癌(BCC)、23例毛发上皮瘤(TE),以及相邻的非肿瘤性皮肤。
II类微管蛋白在颗粒层角质形成细胞、黑素细胞、毛发皮质和角质层细胞、内根鞘(IRS)、外根鞘(ORS)的伴随层(CL)以及具有雪旺氏或肌源性分化的间充质细胞中表达。此外,皮肤肿瘤中鳞状或毛囊分化区域的II类微管蛋白表达增加。在用抗II类微管蛋白对毛囊分化或肌成纤维细胞反应进行分级时,与BCC相比,TE更频繁地表现出毛囊分化(p < 0.001),而肌成纤维细胞反应较少(p = 0.001)。
II类微管蛋白表达与鳞状或毛囊分化密切相关,可能有助于区分大多数SCC与KA以及BCC与TE。然而,它不能可靠地区分高分化的火山口状SCC与KA。