Barricklow Zoe, DiVincenzo Mallory J, Angell Colin D, Carson William E
The Arthur G. James Cancer Hospital and Solove Research Institute, The Ohio, State University, Columbus, OH, USA.
Department of Veterinary Biosciences, The Ohio State University, Columbus, OH, USA.
Clin Cosmet Investig Dermatol. 2022 Aug 30;15:1743-1757. doi: 10.2147/CCID.S372287. eCollection 2022.
The presence of ulceration in melanoma is associated with poor clinical outcomes and is the third most powerful predictor of survival in the AJCC Melanoma Staging System after tumor thickness and mitotic activity. The aggressive biological behavior associated with ulceration has been hypothesized to be the result of an intrinsic biological attribute that favors dissemination and presents locally with the loss of epidermal integrity. Among the features of ulcerated melanoma, many show promise as potential prognostic tools, markers of differential immunogenicity and indicators of oncogenic drivers of invasion and metastasis. The incidence of ulcerated melanoma is greater in males, increases with age and with systemic inflammatory risk factors (diabetes, smoking, low vitamin D, elevated body mass index). Patients with ulcerated primary tumors seem to exclusively benefit from adjuvant interferon (IFN) therapy, which is likely the consequence of an altered tumor microenvironment. When ulceration is present, there is a higher density of macrophages and dendritic cells and enhanced expression of pro-inflammatory cytokines, such as IL-6. There is also an increased expression of proteins involved in tumor antigen presentation in ulcerated melanomas. Histologically, vascular density, vasculogenic mimicry and angiotropism are all significantly correlated with ulceration in melanoma. The presence of ulceration is associated with reduced protein expression of E-cadherin and PTEN and elevated levels of N-cadherin and the matrix metalloproteinases. Differential microRNA expression also holds promise as a potential prognostic biomarker of malignancy and disease spread within the setting of ulceration. However, the molecular and cellular differences associated with the ulcerated state are complex and further study will aid in determining how these differences can be harnessed to improve care for patients with melanoma.
黑色素瘤中溃疡的存在与不良临床结局相关,是美国癌症联合委员会(AJCC)黑色素瘤分期系统中仅次于肿瘤厚度和有丝分裂活性的第三大生存预测指标。与溃疡相关的侵袭性生物学行为被认为是一种内在生物学特性的结果,这种特性有利于肿瘤扩散,并在局部表现为表皮完整性的丧失。在溃疡型黑色素瘤的诸多特征中,许多有望成为潜在的预后工具、免疫原性差异的标志物以及侵袭和转移致癌驱动因素的指标。溃疡型黑色素瘤的发病率男性更高,随年龄增长以及系统性炎症风险因素(糖尿病、吸烟、低维生素D、高体重指数)而增加。原发性肿瘤有溃疡的患者似乎仅从辅助干扰素(IFN)治疗中获益,这可能是肿瘤微环境改变的结果。出现溃疡时,巨噬细胞和树突状细胞密度更高,促炎细胞因子如白细胞介素-6的表达增强。溃疡型黑色素瘤中参与肿瘤抗原呈递的蛋白质表达也增加。组织学上,血管密度、血管生成拟态和血管嗜性均与黑色素瘤中的溃疡显著相关。溃疡的存在与E-钙黏蛋白和PTEN的蛋白表达降低以及N-钙黏蛋白和基质金属蛋白酶水平升高有关。差异微小RNA表达也有望成为溃疡情况下恶性肿瘤和疾病扩散的潜在预后生物标志物。然而,与溃疡状态相关的分子和细胞差异很复杂,进一步研究将有助于确定如何利用这些差异来改善黑色素瘤患者的治疗。