Ferreira S A, Vasconcelos J L A, Cavalcanti C L B, Rêgo M J B, Beltrão E I C
Laboratório de Imunopatologia Keizo Asami (LIKA), Universidade Federal de Pernambuco, Cidade Universitária, Recife, PE, Brazil,
Med Mol Morphol. 2013 Dec;46(4):198-202. doi: 10.1007/s00795-013-0025-0. Epub 2013 Mar 19.
Altered sialylation has been observed during oncogenic transformation and has been implicated in tumor progression and metastases. This pattern may aid the biological behavior of many tumors. Skin cancer is the most common cancer worldwide and their diagnosis becomes difficult, in some cases, due to variety of factors that affect the accuracy of the nowadays exams, such as huge spectrum of tumors and their variants. So, this study investigates the changes in expression and distribution of α2,3 and α2,6-linked sialic acid in non-melanomas skin cancer to identify the sialylation pattern which may be useful in the differential diagnosis of this tumor. Lectin histochemistry was used to examine the expression and distribution of sialic acid in different types of non-melanoma skin cancers. We applied Maackia amurensis lectin, which interacts with α2,3-linked sialic acid and Sambucus nigra lectin specific for α2,6-linked sialic acid. The histochemical analysis showed that α2,3 and α2,6-linked sialic acid vary their expression according with the tumor type analyzed. The distribution of α2,3-linked sialic was differentially expressed in between basal cell carcinoma (BCC) and squamous cell carcinoma (SCC) (p < 0.0001), BCC and actinic keratosis (p = 0.0033) and BCC and keratoacanthoma (p < 0.0001). In the case of α2,6-linked sialic acid its expression was also different between BCC and SCC (p < 0.0001), BCC and actinic keratosis (p = 0.0002) and BCC and keratoacanthoma (p < 0.0362). Lectin histochemistry showed a different expression of both sialic acid linkages types between pre-malign and malign tumors and between malign tumors. Although preliminary, these findings are promising for the development of diagnostic techniques to help in the differential diagnosis of non-melanoma skin tumors using lectin histochemistry as an auxiliary tool.
在致癌转化过程中已观察到唾液酸化改变,且其与肿瘤进展和转移有关。这种模式可能有助于许多肿瘤的生物学行为。皮肤癌是全球最常见的癌症,在某些情况下,由于影响当前检查准确性的多种因素,如肿瘤及其变体的种类繁多,其诊断变得困难。因此,本研究调查非黑素瘤皮肤癌中α2,3和α2,6连接唾液酸的表达和分布变化,以确定可能有助于该肿瘤鉴别诊断的唾液酸化模式。采用凝集素组织化学法检测不同类型非黑素瘤皮肤癌中唾液酸的表达和分布。我们应用了与α2,3连接唾液酸相互作用的东北马兜铃凝集素和对α2,6连接唾液酸具有特异性的黑接骨木凝集素。组织化学分析表明,α2,3和α2,6连接唾液酸的表达随所分析的肿瘤类型而变化。α2,3连接唾液酸的分布在基底细胞癌(BCC)和鳞状细胞癌(SCC)之间(p < 0.0001)、BCC和光化性角化病之间(p = 0.