了解和管理局部晚期基底细胞癌:对发病机制、治疗策略和刺猬通路抑制剂作用的见解。

IF 1.8 4区 医学 Q3 DERMATOLOGY
Marta Cebolla-Verdugo, Carlos Llamas-Segura, Juan P Velasco-Amador, Francisco M Almazán-Fernández, Ricardo Ruiz-Villaverde
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引用次数: 0

摘要

鉴于局部晚期基底细胞癌(BCC)的高发病率和对局部组织造成破坏的可能性,了解和管理局部晚期基底细胞癌至关重要。虽然 BCC 的转移潜力通常较低,但其高发病率凸显了加强治疗策略的必要性。局部晚期 BCC 带来了独特的挑战,通常需要积极干预以防止毁容和功能障碍。刺猬通路抑制剂(HHIs)的出现通过靶向刺猬信号传导异常(BCC发病机制的关键驱动因素)提供了前景广阔的治疗途径。因此,阐明局部晚期 BCC 的发病机制并探索 HHIs 的作用是有效治疗这种流行性癌症的关键。从流行病学角度看,BCC 主要影响皮肤白皙、长期暴露于阳光下的人群,年轻群体的发病率呈上升趋势。风险因素包括紫外线照射、家族性皮肤癌病史、免疫抑制以及遗传综合征,如基底细胞痣综合征和色素性皮肤病。从病理上讲,BCC 来自皮肤表皮细胞,主要的遗传驱动因素是刺猬通路的激活,涉及 PTCH1 和 SMO 的突变。由于基因变化,患者可能会对刺猬抑制剂产生抗药性,从而使治疗策略复杂化。BCC 的特点是免疫原性低,这阻碍了免疫反应,也给治疗带来了挑战。加强对局部晚期 BCC 的流行病学、风险因素和发病机制的了解,以及开发刺猬蛋白通路抑制剂等靶向治疗方法,对于有效控制这种流行性癌症和改善患者预后至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Understanding and managing locally advanced basal cell carcinoma: insights into pathogenesis, therapeutic strategies, and the role of hedgehog pathway inhibitors.

Understanding and managing locally advanced basal cell carcinoma (BCC) is crucial given its substantial prevalence and potential for local tissue destruction. While BCC typically exhibits low metastatic potential, its high incidence underscores the need for enhanced therapeutic strategies. Locally advanced BCC presents unique challenges, often necessitating aggressive interventions to prevent disfigurement and functional impairment. The emergence of hedgehog pathway inhibitors (HHIs) offers promising therapeutic avenues by targeting aberrant hedgehog signaling, a key driver in BCC pathogenesis. Thus, elucidating the pathogenesis of locally advanced BCC and exploring the role of HHIs are critical endeavors in effectively managing this prevalent carcinoma. Epidemiologically, BCC primarily affects individuals with fair skin and chronic sun exposure, with an increasing incidence noted among younger age groups. Risk factors include UV radiation exposure, familial history of skin cancer, immunosuppression, and genetic syndromes such as basal cell nevus syndrome and xeroderma pigmentosum. Pathogenetically, BCC arises from cells in the skin's epidermis, with hedgehog pathway activation being a primary genetic driver, involving mutations in PTCH1 and SMO. Resistance to hedgehog inhibitors may occur due to genetic changes, complicating treatment strategies. BCC is characterized by low immunogenicity, which hinders immune response and contributes to treatment challenges. Enhanced understanding of the epidemiology, risk factors, and pathogenesis of locally advanced BCC, along with the development of targeted therapeutic approaches such as hedgehog pathway inhibitors, is essential for effectively managing this prevalent carcinoma and improving patient outcomes.

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CiteScore
3.10
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