首页> 美国卫生研究院文献>European Journal of Histochemistry : EJH >Expression patterns of α23-Sialyltransferase I and α26-Sialyltransferase I in human cutaneous epithelial lesions
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Expression patterns of α23-Sialyltransferase I and α26-Sialyltransferase I in human cutaneous epithelial lesions

机译:α23-唾液酸转移酶I和α26-唾液酸转移酶I在人皮肤上皮病变中的表达模式

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摘要

Skin tumors have become one of the most common cancers in the world and their carcinogenesis is frequently associated with altered glycosylation patterns. The aberrant sialylation, a type of glycosylation, can mediate pathophysiological key events during various stages of tumor progression, including invasion and metastasis. Sialyltransferases play a key role in a variety of biological processes, including cell-cell communication, cell-matrix interaction, adhesion, and protein targeting. In this study, it was evaluated the expression of ST3Gal I and ST6Gal I in cutaneous epithelial lesions that include actinic keratosis (n=15), keratoacanthoma (n=9), squamous cell carcinoma (n=22) and basal cell carcinoma (n=28) in order to evaluate if sialyltransferases expression is different in premalignant and in malignant tumors. The expression of ST3Gal I was observed in actinic keratosis (53%), keratoacanthoma (78%), squamous cell carcinoma (73%) and basal cell carcinoma (32%) with statistic differences between basal cell carcinoma and keratoacanthoma (P=0.0239) and basal cell carcinoma and squamous cell carcinoma (P=0.0096); for ST6Gal I, cytoplasmic expression was noted in actinic keratosis (40%), heterogeneous and cytoplasmic expression was noted in keratoacanthoma (67%), squamous cell carcinoma (41%) and basal cell carcinoma (7%) with statistic differences between basal cell carcinoma and squamous cell carcinoma (P=0.0061) and basal cell carcinoma and keratoacanthoma (P=0.0008). In summary, our results showed that the high expression of ST3Gal I and ST6Gal I, in skin tumors, is associated with tumors with greater potential for invasion and metastasis, as in the case of squamous cell carcinoma, and this may be related to their behavior.
机译:皮肤肿瘤已成为世界上最常见的癌症之一,其致癌作用通常与糖基化模式的改变有关。异常的唾液酸化(一种糖基化)可以在肿瘤进展的各个阶段(包括侵袭和转移)中介导病理生理关键事件。唾液酸转移酶在多种生物学过程中起关键作用,包括细胞与细胞之间的通讯,细胞与基质的相互作用,粘附和蛋白质靶向。在这项研究中,我们评估了ST3Gal I和ST6Gal I在包括光化性角化病(n = 15),角化棘皮瘤(n = 9),鳞状细胞癌(n = 22)和基底细胞癌(n = 28),以评估唾液酸转移酶在恶性肿瘤前和恶性肿瘤中的表达是否不同。 ST3Gal I的表达在光化性角化病(53%),角化棘皮瘤(78%),鳞状细胞癌(73%)和基底细胞癌(32%)中观察到,基底细胞癌和角化棘皮瘤之间的统计学差异(P = 0.0239)基底细胞癌和鳞状细胞癌(P = 0.0096);对于ST6Gal I,在光化性角化病(40%)中注意到细胞质表达,在角棘皮瘤(67%),鳞状细胞癌(41%)和基底细胞癌(7%)中注意到异质和胞质表达,基底细胞之间的统计差异癌和鳞状细胞癌(P = 0.0061)和基底细胞癌和角棘皮瘤(P = 0.0008)。总之,我们的结果表明,如皮肤鳞状细胞癌,ST3Gal I和ST6Gal I在皮肤肿瘤中的高表达与肿瘤具有更大的侵袭和转移潜能有关,这可能与其行为有关。

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