Biochemical pathways and targeted therapies in basal cell carcinoma: A systematic review

B. Tran, Tiffany Alexander, A. Somani
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引用次数: 2

Abstract

Basal cell carcinoma (BCC) is the most common type of human malignancy. It is a slow-growing skin cancer with little ability to metastasize, but it is aggressive and can cause local tissue destruction. Descriptions of Basal Cell Nevus Syndrome (BCNS), characterized by a predisposition to the formation of BCC and other neoplasms, and identification of the genetic defect in this syndrome, has led to significant advancement in our understanding of the pathogenesis of BCC. Unregulated expression of target genes in the sonic Hedgehog (SHH) signaling pathway plays a prominent role in the pathogenesis of BCC. An understanding of the signaling components has allowed for the development of pharmacologic agents that inhibit the SHH pathway. The first inhibitor of the SHH pathway approved by the Food and Drug Administration (FDA) for the treatment of BCC is vismodegib. In this review, we will discuss the biochemical pathways involved in BCC as targets of novel pharmacologic therapies.
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基底细胞癌的生化途径和靶向治疗:系统综述
基底细胞癌(BCC)是人类最常见的恶性肿瘤。这是一种生长缓慢的皮肤癌,几乎没有转移的能力,但它具有侵袭性,可以导致局部组织破坏。基底细胞痣综合征(Basal Cell neus Syndrome, BCNS)具有形成基底细胞癌和其他肿瘤的易感性,对其的描述以及对该综合征遗传缺陷的识别,使我们对基底细胞癌发病机制的理解取得了重大进展。sonic Hedgehog (SHH)信号通路中靶基因的不调节表达在BCC的发病机制中起着重要作用。对信号传导成分的理解使得开发抑制SHH通路的药物成为可能。美国食品和药物管理局(FDA)批准用于治疗BCC的首个SHH通路抑制剂是vismodegib。在这篇综述中,我们将讨论作为新型药物治疗靶点的BCC的生化途径。
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