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在实验性小鼠模型的进行性皮肤癌发生过程中,FGFR2和NOTCH1表达呈负相关。

FGFR2 and NOTCH1 Expression Inversely Correlated in Progressive Cutaneous Carcinogenesis in an Experimental Mouse Model.

作者信息

Vairaktari Georgia, Schramm Alexander, Vairaktari Efstathia, Derka Spyridoula, Sakkas Andreas, Lefantzis Nikolaos, Diamantopoulou Stavroula, Vylliotis Antonis, Lazaris Andreas, Ebeling Marcel, Vassiliou Stavros

机构信息

Department of Oral and Maxillofacial Surgery, University General Hospital Attikon, School of Medicine, National and Kapodistrian University of Athens, 11527 Athens, Greece.

Department of Oral and Maxillofacial Surgery, University Hospital Ulm, Albert-Einstein-Allee 10, 89081 Ulm, Germany.

出版信息

J Pers Med. 2024 Jul 5;14(7):729. doi: 10.3390/jpm14070729.

DOI:10.3390/jpm14070729
PMID:39063983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11277703/
Abstract

Cutaneous squamous cell carcinoma (cSCC) is a common and increasingly prevalent form of skin cancer, posing significant health challenges. Understanding the molecular mechanisms involved in cSCC progression is crucial for developing effective treatments. The primary aim of this research was to evaluate the activation of NOTCH1 and FGFR2 oncogenes in inducing skin cancer in FVB/N mice through a stepwise chemical process. Forty female FVB/N mice, aged four weeks, were randomly divided into a control group (n = 8) and two experimental groups (group A: n = 16, group B: n = 16). This study involved subjecting the groups to a two-stage carcinogenesis procedure. This included an initial application of 97.4 nmol DMBA on shaved skin on their backs, followed by applications of 32.4 nmol TPA after thirteen weeks for group A and after twenty weeks for group B. The control group did not receive any treatment. Their skin conditions were monitored weekly to detect tumor development. After the experiment, the animals were euthanized for further tissue sampling. The examination of skin lesions in the experimental groups showed a correlation with tumor progression, ranging from dysplasia to carcinoma. Tumor samples were assessed both histologically and immunohistochemically. Notably, FGFR2 expression was higher in benign, precancerous, and malignant tumors compared to normal tissue. NOTCH1 expression was only elevated in benign tumors compared to normal tissue. This study demonstrates a clear correlation of FGFR2 expression and the progression of cutaneous neoplasms, while NOTCH 1 expression is inversely correlated in FVB/N mice. This suggests an early involvement of these oncogenes in the development of skin tumors.

摘要

皮肤鳞状细胞癌(cSCC)是一种常见且日益普遍的皮肤癌形式,带来了重大的健康挑战。了解cSCC进展所涉及的分子机制对于开发有效的治疗方法至关重要。本研究的主要目的是通过逐步化学过程评估NOTCH1和FGFR2癌基因在诱导FVB/N小鼠皮肤癌中的激活情况。40只四周龄的雌性FVB/N小鼠被随机分为对照组(n = 8)和两个实验组(A组:n = 16,B组:n = 16)。本研究涉及对这些组进行两阶段致癌程序。这包括首先在其背部剃毛的皮肤上涂抹97.4 nmol的二甲基苯并蒽(DMBA),然后A组在13周后、B组在20周后涂抹32.4 nmol的佛波酯(TPA)。对照组未接受任何处理。每周监测它们的皮肤状况以检测肿瘤发展。实验结束后,对动物实施安乐死以进行进一步的组织采样。实验组皮肤病变检查显示与肿瘤进展相关,范围从发育异常到癌。对肿瘤样本进行了组织学和免疫组织化学评估。值得注意的是,与正常组织相比,FGFR2在良性、癌前和恶性肿瘤中的表达更高。与正常组织相比,NOTCH1仅在良性肿瘤中表达升高。本研究表明FGFR2表达与皮肤肿瘤进展存在明显相关性,而在FVB/N小鼠中NOTCH 1表达呈负相关。这表明这些癌基因在皮肤肿瘤发展中早期就发挥了作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa44/11277703/ec5bae95df0b/jpm-14-00729-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa44/11277703/46beb479b25e/jpm-14-00729-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa44/11277703/03e249da0edc/jpm-14-00729-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa44/11277703/1b61834de2bc/jpm-14-00729-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa44/11277703/ec5bae95df0b/jpm-14-00729-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa44/11277703/46beb479b25e/jpm-14-00729-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa44/11277703/03e249da0edc/jpm-14-00729-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa44/11277703/1b61834de2bc/jpm-14-00729-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa44/11277703/ec5bae95df0b/jpm-14-00729-g004.jpg

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1
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Mol Cancer. 2023 Jan 12;22(1):10. doi: 10.1186/s12943-022-01708-4.
2
Method to Study Skin Cancer: Two-Stage Chemically Induced Carcinogenesis in Mouse Skin.研究皮肤癌的方法:小鼠皮肤的两阶段化学诱导癌变。
Methods Mol Biol. 2020;2154:231-238. doi: 10.1007/978-1-0716-0648-3_19.
3
The Hamster Model of Sequential Oral Carcinogenesis: An Update.序贯口腔致癌的仓鼠模型:更新。
In Vivo. 2019 Nov-Dec;33(6):1751-1755. doi: 10.21873/invivo.11665.
4
Targeting Cellular Trafficking of Fibroblast Growth Factor Receptors as a Strategy for Selective Cancer Treatment.靶向成纤维细胞生长因子受体的细胞转运作为选择性癌症治疗策略
J Clin Med. 2018 Dec 20;8(1):7. doi: 10.3390/jcm8010007.
5
Making way for suppressing the FGF19/FGFR4 axis in cancer.为抑制癌症中的 FGF19/FGFR4 轴铺平道路。
Future Med Chem. 2018 Oct;10(20):2457-2470. doi: 10.4155/fmc-2018-0099. Epub 2018 Oct 16.
6
FGF2 and EGF induce epithelial-mesenchymal transition in malignant pleural mesothelioma cells via a MAPKinase/MMP1 signal.FGF2 和 EGF 通过 MAPKinase/MMP1 信号诱导恶性胸膜间皮瘤细胞发生上皮-间充质转化。
Carcinogenesis. 2018 Apr 5;39(4):534-545. doi: 10.1093/carcin/bgy018.
7
Management of Metastatic Melanoma in 2018.2018年转移性黑色素瘤的管理
JAMA Oncol. 2018 Jun 1;4(6):857-858. doi: 10.1001/jamaoncol.2018.0170.
8
-mutant melanoma: current challenges and future prospect.- 突变型黑色素瘤:当前挑战与未来展望
Onco Targets Ther. 2017 Aug 8;10:3941-3947. doi: 10.2147/OTT.S117121. eCollection 2017.
9
Survival of patients with advanced metastatic melanoma: the impact of novel therapies-update 2017.晚期转移性黑色素瘤患者的生存情况:新型疗法的影响——2017年更新
Eur J Cancer. 2017 Sep;83:247-257. doi: 10.1016/j.ejca.2017.06.028. Epub 2017 Aug 23.
10
The new paradigm of systemic therapies for metastatic melanoma.转移性黑色素瘤的系统性治疗新范例。
J Am Acad Dermatol. 2017 Aug;77(2):356-368. doi: 10.1016/j.jaad.2017.04.1126.