Suppr超能文献

GBP1 通过激活 SP1 促进皮肤鳞状细胞癌的增殖和侵袭。

GBP1 promotes cutaneous squamous cell carcinoma proliferation and invasion through activation of STAT3 by SP1.

机构信息

Department of Burns and Plastic Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, P.R. China.

出版信息

Exp Dermatol. 2024 Jun;33(6):e15112. doi: 10.1111/exd.15112.

Abstract

Cutaneous squamous cell carcinoma (cSCC) ranks as the second most prevalent skin tumour (excluding melanoma). However, the molecular mechanisms driving cSCC progression remain elusive. This study aimed to investigate GBP1 expression in cSCC and elucidate its potential molecular mechanisms underlying cSCC development. GBP1 expression was assessed across public databases, cell lines and tissue samples. Various assays, including clone formation, CCK8 and EdU were employed to evaluate cell proliferation, while wound healing and transwell assays determined cell migration and invasion. Subcutaneous tumour assays were conducted to assess in vivo tumour proliferation, and molecular mechanisms were explored through western blotting, immunofluorescence and immunoprecipitation. Results identified GBP1 as an oncogene in cSCC, with elevated expression in both tumour tissues and cells, strongly correlating with tumour stage and grade. In vitro and in vivo investigations revealed that increased GBP1 expression significantly enhanced cSCC cell proliferation, migration and invasion. Mechanistically, GBP1 interaction with SP1 promoted STAT3 activation, contributing to malignant behaviours. In conclusion, the study highlights the crucial role of the GBP1/SP1/STAT3 signalling axis in regulating tumour progression in cSCC. These findings provide valuable insights into the molecular mechanisms of cSCC development and offer potential therapeutic targets for interventions against cSCC.

摘要

皮肤鳞状细胞癌 (cSCC) 是第二大常见皮肤肿瘤(不包括黑色素瘤)。然而,驱动 cSCC 进展的分子机制仍不清楚。本研究旨在研究 cSCC 中 GBP1 的表达,并阐明其在 cSCC 发展中的潜在分子机制。评估了公共数据库、细胞系和组织样本中的 GBP1 表达。通过克隆形成、CCK8 和 EdU 等各种测定来评估细胞增殖,而通过划痕愈合和 Transwell 测定来确定细胞迁移和侵袭。进行了皮下肿瘤测定以评估体内肿瘤增殖,并通过 Western blot、免疫荧光和免疫沉淀来探索分子机制。结果确定 GBP1 是 cSCC 的致癌基因,在肿瘤组织和细胞中均呈高表达,与肿瘤分期和分级强烈相关。体外和体内研究表明,GBP1 表达增加可显著增强 cSCC 细胞的增殖、迁移和侵袭。机制上,GBP1 与 SP1 的相互作用促进了 STAT3 的激活,导致恶性行为。总之,该研究强调了 GBP1/SP1/STAT3 信号轴在调节 cSCC 肿瘤进展中的关键作用。这些发现为 cSCC 发展的分子机制提供了有价值的见解,并为针对 cSCC 的干预提供了潜在的治疗靶点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验