Lee C S, Redshaw A, Boag G
Department of Pathology, University of Melbourne, St George Hospital, Kogarah, New South Wales, Australia.
Aust N Z J Surg. 1996 Jul;66(7):464-8. doi: 10.1111/j.1445-2197.1996.tb00783.x.
Transforming growth factor alpha (TGF-alpha) is a polypeptide that is structurally similar to epidermal growth factor (EGF) that binds to the epidermal growth factor receptor (EGFR) and has been implicated in the development of several types of human tumours.
The expression of TGF-alpha is examined in laryngeal squamous cell carcinoma (SCC) (n = 24) and non-neoplastic polyps (n = 7) using streptavidin-biotin immunohistochemistry and a monoclonal antibody to the TGF-alpha protein. These cases had been previously characterized for EGFR immunoreactivity. The carcinomas were classified as well differentiated (n = 2), moderately differentiated (n = 16) and poorly differentiated (n = 6). Tissues from metastatic tumour deposits in lymph nodes (n = 5) were also studied.
TGF-alpha overexpression was defined as intense immunoreactivity in more than two-thirds of tumour cells immunostained for TGF-alpha and was present in the majority of the SCC cases (n = 15; 63%) and metastatic tumour deposits (n = 4; 80%). In contrast, although some of the vocal cord polyps showed weak (n = 2) to moderate (n = 5) immunostaining, none had evidence of strong TGF-alpha immunoreactivity. The differences in TGF-alpha immunoreactivity were significant between primary laryngeal SCC and vocal cord polyps (P = 0.013; chi 2 test with continuity correction), and between metastatic laryngeal SCC and vocal cord polyps (P = 0.023; chi 2 test with continuity correction). There was no significant difference in TGF-alpha expression between the different grades of carcinomas (P = 0.92, chi 2 test) or between non-metastatic and metastatic carcinomas (P = 0.82; chi 2 test with continuity correction). No significant correlation was found between TGF-alpha expression and patient survival or tumour recurrence (r = 0.077, r2 = 0.006, P = 0.75; simple regression analysis), or between TGF-alpha expression and EGFR immunoreactivity (r = 0.325, r2 = 0.106, P = 0.0851).
In conclusion, increased TGF-alpha immunoreactivity is present in most cases of laryngeal SCC with no specific relationship to tumour grade, suggesting that it may be important in the development of laryngeal carcinomas but not in its progression. No significant correlation was found between TGF-alpha and EGFR expression in laryngeal tumours and TGF-alpha immunoreactivity is of no prognostic value.
转化生长因子α(TGF-α)是一种多肽,其结构与表皮生长因子(EGF)相似,能与表皮生长因子受体(EGFR)结合,并且与多种类型人类肿瘤的发生有关。
使用链霉亲和素-生物素免疫组织化学和针对TGF-α蛋白的单克隆抗体,检测24例喉鳞状细胞癌(SCC)和7例非肿瘤性息肉中TGF-α的表达。这些病例先前已进行EGFR免疫反应性的特征分析。癌组织分为高分化(n = 2)、中分化(n = 16)和低分化(n = 6)。还研究了来自淋巴结转移瘤灶的组织(n = 5)。
TGF-α过表达定义为在三分之二以上经TGF-α免疫染色的肿瘤细胞中出现强免疫反应性,多数SCC病例(n = 15;63%)和转移瘤灶(n = 4;80%)中存在TGF-α过表达。相比之下,尽管一些声带息肉显示出弱(n = 2)至中度(n = 5)免疫染色,但均无TGF-α强免疫反应性的证据。原发性喉SCC与声带息肉之间以及转移性喉SCC与声带息肉之间TGF-α免疫反应性的差异具有统计学意义(P = 0.013;连续性校正卡方检验)。不同分级的癌之间(P = 0.92,卡方检验)或非转移性癌与转移性癌之间(P = 0.82;连续性校正卡方检验)TGF-α表达无显著差异。未发现TGF-α表达与患者生存率或肿瘤复发之间存在显著相关性(r = 0.077,r2 = 0.006,P = 0.75;简单回归分析),也未发现TGF-α表达与EGFR免疫反应性之间存在显著相关性(r = 0.325,r2 = 0.106,P = 0.0851)。
总之,大多数喉SCC病例中TGF-α免疫反应性增加,与肿瘤分级无特定关系,这表明其可能在喉癌发生中起重要作用,但在其进展中并非如此。未发现喉肿瘤中TGF-α与EGFR表达之间存在显著相关性,且TGF-α免疫反应性无预后价值。