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瞬时受体电位通道亚家族 M 成员 8(TRPM8)在非黑素细胞皮肤癌中的表达:一项临床和免疫组化研究。

Expression of Transient Receptor Potential Channel of Melastatin number 8 (TRPM8) in Non- Melanoma Skin Cancer: A Clinical and Immunohistochemical study.

机构信息

Pathology Department, Faculty of Medicine, Menoufia University, Shebin El Kom, Egypt.

Dermatology Department, Faculty of Medicine, Menoufia University, Shebin El Kom, Egypt.

出版信息

J Immunoassay Immunochem. 2021 Nov 2;42(6):620-632. doi: 10.1080/15321819.2021.1918709. Epub 2021 Apr 25.

Abstract

Transient Receptor Potential Channel of Melastatin number 8 (TRPM8) is abnormally expressed in many cancers as lung, however little is known about TRPM8 expression in non-melanoma skin cancer (NMSC) including cutaneous squamous cell carcinoma (SCC) and basal cell carcinoma (BCC). This work aimed to study TRPM8 expression in NMSC. It included 100 skin biopsies (50 normal skin as control group, 15 BCC and 35 SCC). Immunohistochemical staining for TRPM8 was done and results were correlated with clinicopathological characters. There was significant higher TRPM8 H-score in NMSC than control skin. On comparing SCC cases to control, there was significant positive TRPM8 expression, strong intensity, diffuse pattern, cytoplasmic and nucleo-cytoplasmic localization and higher range of H-score in SCC. In contrast, BCC showed significant lower TRPM8 positive expression when compared to control skin. Higher TRPM8 H-score in SCC showed significant positive correlation with large tumor size and poor tumor differentiation.TRPM8 may be implicated in pathogenesis of NMSC. Its association with bad prognostic characters; potentiates its role as prognostic biomarker and open new chances for therapeutic intervention in NMSC. TRPM8 antagonists may share in decreasing tumor growth and progression and may serve as potential target for tumor immunotherapy.

摘要

瞬时受体电位通道 M 亚家族成员 8(TRPM8)在许多癌症中异常表达,如肺癌,但在非黑色素瘤皮肤癌(NMSC)中,包括皮肤鳞状细胞癌(SCC)和基底细胞癌(BCC)中,TRPM8 的表达情况知之甚少。本研究旨在研究 NMSC 中 TRPM8 的表达情况。纳入 100 例皮肤活检标本(50 例正常皮肤作为对照组,15 例 BCC 和 35 例 SCC)。进行 TRPM8 免疫组织化学染色,并将结果与临床病理特征进行相关性分析。与正常皮肤相比,NMSC 中 TRPM8 的 H 评分显著升高。将 SCC 病例与对照组相比,SCC 中 TRPM8 的表达显著阳性,强度较强,呈弥漫性模式,定位于细胞质和核质,H 评分范围较高。相比之下,与正常皮肤相比,BCC 中 TRPM8 的阳性表达显著降低。SCC 中较高的 TRPM8 H 评分与较大的肿瘤大小和较差的肿瘤分化呈显著正相关。TRPM8 可能与 NMSC 的发病机制有关。其与不良预后特征的相关性使其具有作为预后生物标志物的潜力,并为 NMSC 的治疗干预开辟了新的机会。TRPM8 拮抗剂可能有助于减少肿瘤的生长和进展,并可能成为肿瘤免疫治疗的潜在靶点。

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