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微囊性附属器癌中 Hedgehog 信号分子的表达。

Expression of Hedgehog signalling molecules in microcystic adnexal carcinoma.

机构信息

Skin Cancer Center, Department of Dermatology, Ruhr-University Bochum, Bochum, Germany.

Dermatopathology Duisburg, Duisburg, Germany.

出版信息

Clin Exp Dermatol. 2021 Aug;46(6):1052-1057. doi: 10.1111/ced.14634. Epub 2021 May 1.

Abstract

BACKGROUND

Microcystic adnexal carcinoma (MAC) is a rare skin neoplasm that has not been characterized on a molecular basis.

AIM

To assess expression profiles of Hedgehog (HH) signalling molecules in MAC and control tumours.

METHODS

Immunohistochemistry was performed for Sonic Hedgehog (SHH), Indian Hedgehog (IHH), Patched 1 (PTCH1) and Smoothened (SMO) on patient MAC tissue (n = 26) and control tumour tissue, including syringoma (SyG; n = 11), trichoepithelioma (TE; n = 11) and basal cell carcinoma (BCC; n = 12) tissues.

RESULTS

Patched 1 and SMO immunoreactivity was significantly higher in BCC than in SyG, TE or MAC (P < 0.001 and P < 0.03, respectively). The highest IHH expression was observed in BCC and TE compared with SyG and MAC (P < 0.04). Notably, the highest SHH protein expression was observed in SyG compared with MAC, TE and even BCC (P < 0.001). In patients with MAC, SMO immunoreactivity significantly (r = 0.51; P < 0.01) correlated with PTCH1 expression. Further correlation studies did not show significant associations between the HH expression markers assessed (P > 0.05).

CONCLUSION

Our results indicate that alterations of the HH signalling are unlikely to play a major role in the pathogenesis of MAC, which is in contrast to the morphologically similar BCC and TE. Our observation provides additional information to the limited molecular pathology knowledge on this rare tumour.

摘要

背景

微囊性附属器癌(MAC)是一种罕见的皮肤肿瘤,尚未在分子基础上进行特征描述。

目的

评估 Hedgehog(HH)信号分子在 MAC 和对照肿瘤中的表达谱。

方法

对 26 例 MAC 组织和 11 例汗腺瘤(SyG)、11 例毛发上皮瘤(TE)和 12 例基底细胞癌(BCC)对照肿瘤组织中的 Sonic Hedgehog(SHH)、Indian Hedgehog(IHH)、Patched 1(PTCH1)和 Smoothened(SMO)进行免疫组织化学染色。

结果

PTCH1 和 SMO 免疫反应性在 BCC 中显著高于 SyG、TE 或 MAC(P<0.001 和 P<0.03)。在 BCC 和 TE 中观察到最高的 IHH 表达,与 SyG 和 MAC 相比(P<0.04)。值得注意的是,在 SyG 中观察到最高的 SHH 蛋白表达,与 MAC、TE 甚至 BCC 相比(P<0.001)。在 MAC 患者中,SMO 免疫反应性与 PTCH1 表达显著相关(r=0.51;P<0.01)。进一步的相关性研究表明,评估的 HH 表达标志物之间没有显著关联(P>0.05)。

结论

我们的结果表明,HH 信号的改变不太可能在 MAC 的发病机制中起主要作用,这与形态上相似的 BCC 和 TE 不同。我们的观察结果为这种罕见肿瘤的有限分子病理学知识提供了额外的信息。

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