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上皮和基质层黏蛋白-1 和 -2 在口腔和皮肤鳞状细胞癌中表达明显。

Epithelial and stromal syndecan-1 and -2 are distinctly expressed in oral- and cutaneous squamous cell carcinomas.

机构信息

Institute of Dentistry, University of Helsinki, Helsinki, Finland.

出版信息

J Oral Pathol Med. 2013 May;42(5):389-95. doi: 10.1111/jop.12025. Epub 2012 Dec 21.

Abstract

BACKGROUND

Oral squamous cell carcinoma (OSCC) and cutaneous squamous cell carcinoma (CSCC) are epithelial neoplasms of which OSCC has worse survival and higher risk of metastasis than CSCC. The aim of this study was to explore the differences of immunoexpressions between syndecan-1 and -2 in OSCC and head and neck CSCC.

METHODS

A total of 35 patients diagnosed with OSCC and 25 with CSCC, presented T1 and T2 tumors and treated at Helsinki University Central Hospital between years 2001 and 2009, were selected into this study. The levels and locations of syndecan-1 and -2 immunostainings were analyzed using formalin-fixed and paraffin-embedded tissue samples of OSCC and CSCC cases together with clinical data.

RESULTS

Cell membrane epithelial syndecan-1 expression decreased significantly compared to normal tissue in both cancer types. Cell membrane syndecan-1 expression in the invasive front had negative correlation with invasion depth of both tumors (OSCC, r = -0.339, P = 0.025; CSCC, r = -0.469, P = 0.004). In cancers over 4-mm invasion depth, the number of stromal syndecan-1-positive collagen fibers and inflammatory cells were higher in OSCC than in CSCC. Syndecan-2 expression in non-malignant stroma was higher in CSCC than in OSCC tumors. In addition, unlike syndecan-1, syndecan-2 was more often and more intensively expressed in the tumor inflammatory cells in CSCC than in OSCC.

CONCLUSION

Our results suggest that variable stromal expression of syndecan-1 and -2 in OSCC compared to CSCC may at least partially explain the differences in their clinical behavior.

摘要

背景

口腔鳞状细胞癌(OSCC)和皮肤鳞状细胞癌(CSCC)是上皮性肿瘤,其中 OSCC 的生存率更差,转移风险更高。本研究旨在探讨 OSCC 和头颈部 CSCC 中 syndecan-1 和 -2 的免疫表达差异。

方法

选择 2001 年至 2009 年间在赫尔辛基大学中心医院就诊的 35 例 OSCC 和 25 例 CSCC 患者,这些患者均诊断为 T1 和 T2 期肿瘤。使用福尔马林固定石蜡包埋的 OSCC 和 CSCC 组织样本及临床资料分析 syndecan-1 和 -2 免疫染色的水平和位置。

结果

与正常组织相比,两种癌症的细胞膜上皮 syndecan-1 表达均显著降低。两种肿瘤侵袭前沿的细胞膜 syndecan-1 表达与侵袭深度呈负相关(OSCC,r = -0.339,P = 0.025;CSCC,r = -0.469,P = 0.004)。在侵袭深度超过 4mm 的癌症中,OSCC 中的基质 syndecan-1 阳性胶原纤维和炎症细胞数量高于 CSCC。CSCC 肿瘤中非恶性基质中的 syndecan-2 表达高于 OSCC 肿瘤。此外,与 syndecan-1 不同,CSCC 中的肿瘤炎症细胞中 syndecan-2 的表达更频繁且更强烈,而 OSCC 中的表达则不然。

结论

我们的研究结果表明,与 CSCC 相比,OSCC 中基质 syndecan-1 和 -2 的可变表达至少部分解释了它们临床行为的差异。

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