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Dab2 调控皮肤鳞状细胞癌的肿瘤进展。

Disabled 2 (Dab2) Regulates Tumour Progression in Skin Squamous Cell Carcinoma.

机构信息

Stem Cell Biology Group, Waghmare Lab, Cancer Research Institute, Advanced Centre for Treatment Research and Education in Cancer (ACTREC), Tata Memorial Centre, Navi Mumbai, Maharashtra, India.

Homi Bhabha National Institute, Training School Complex, Mumbai, India.

出版信息

Exp Dermatol. 2024 Nov;33(11):e70009. doi: 10.1111/exd.70009.

Abstract

Dab2 is an endocytic adaptor protein involved in various physiological processes and signaling pathways. Dab2 is deregulated in various cancers; however, its role in skin squamous cell carcinoma ( SCC) has not been elucidated yet. In the present study, we used the DMBA/TPA induced murine skin carcinogenesis model to examine the role of Dab2 in skin tumour progression. We generated tamoxifen inducible Dab2 conditional knockout system for our study. Loss of Dab2 led to delayed papilloma initiation and reduced papilloma burden. Delayed papilloma initiation was due to reduce proliferative potential of the papillomas due to Dab2 loss. Furthermore, while the WT papillomas progressed to SCC, the papillomas formed in Dab2 cKO mice failed to undergo malignant conversion to SCC. Dab2 cKO tumours showed reduced expression of K8, a marker for aggressive tumour. Moreover, Dab2 ckO tumours failed to undergo EMT as shown by reduced expression of Vimentin and Twist1. Dab2 cKO tumours also showed reduced expression of Sox2, a stem cell marker. Furthermore, qPCR analysis showed upregulation of Dab2 expression in the human skin cancer cell lines as compared to normal human skin keratinocytes. In patients, TCGA data analysis of skin cancer melanoma (SKCM) showed a trend where high levels of Dab2 correlated with poor overall survival. The present study shows that Dab2 promotes tumour progression in skin SCC.

摘要

Dab2 是一种参与多种生理过程和信号通路的内吞衔接蛋白。Dab2 在各种癌症中失调;然而,其在皮肤鳞状细胞癌(SCC)中的作用尚未阐明。在本研究中,我们使用 DMBA/TPA 诱导的小鼠皮肤致癌模型来研究 Dab2 在皮肤肿瘤进展中的作用。我们为研究生成了可诱导型 Dab2 条件性敲除系统。Dab2 的缺失导致了乳头状瘤起始的延迟和乳头状瘤负担的减少。乳头状瘤起始的延迟是由于 Dab2 缺失导致了乳头状瘤的增殖潜力降低。此外,虽然 WT 乳头状瘤进展为 SCC,但 Dab2 cKO 小鼠中形成的乳头状瘤未能发生恶性转化为 SCC。Dab2 cKO 肿瘤显示出 K8 的表达减少,K8 是一种侵袭性肿瘤的标志物。此外,Dab2 ckO 肿瘤未能发生 EMT,表现为 Vimentin 和 Twist1 的表达减少。Dab2 cKO 肿瘤也显示出 Sox2 的表达减少,Sox2 是一种干细胞标志物。此外,qPCR 分析显示,与正常人类皮肤角质形成细胞相比,人类皮肤癌细胞系中 Dab2 的表达上调。在患者中,TCGA 皮肤癌黑色素瘤(SKCM)数据分析显示,高水平的 Dab2 与整体生存不良相关。本研究表明 Dab2 促进皮肤 SCC 中的肿瘤进展。

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