皮肤基底细胞癌中IMP3的免疫组织化学表达

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL Galician Medical Journal Pub Date : 2022-09-01 DOI:10.21802/gmj.2022.3.1
V. Bartoš
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引用次数: 0

摘要

背景胰岛素样生长因子II mRNA结合蛋白3(IMP3)是一种在肿瘤细胞癌变过程中上调的癌胚蛋白。它与许多恶性肿瘤的不良临床结果有关。本研究旨在评估IMP3在皮肤基底细胞癌(BCC)中的免疫组织化学表达状态,并将其与Ki-67指标值相关联。方法。本分析纳入了32例基底细胞癌的活检标本。对所有样品进行IMP3(克隆69.1)和Ki-67抗原(克隆MIB-1)的免疫组化染色。后果IMP3弱表达11例(34.4%),中度表达11例,强表达5例(15.6%),阴性染色5例(15.2%)。在表现出侵袭性生长特征的7个BCC中,除1个外,其余均表现出弱反应性。相反,所有五个表现出强IMP3阳性的基底细胞癌均由惰性生长组织学亚型组成。具有浸润性组织形态学的基底细胞癌似乎没有产生更显著IMP3的趋势。IMP3的表达状态与肿瘤组织的增殖状态(Ki-67≤50%,Ki-67>50%)无显著关系(p>0.05)。绝大多数皮肤基底细胞癌表达IMP3,这表明这种癌蛋白与基底细胞癌的致癌作用有关。然而,更显著的表达似乎与BCC的侵袭性生长表型或肿瘤细胞的更高增殖活性无关。
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Immunohistochemical Expression of IMP3 in Cutaneous Basal Cell Carcinoma
Background. Insulin-like growth factor-II mRNA-binding protein 3 (IMP3) is an oncofetal protein upregulated in tumor cells during carcinogenesis. It has been linked to adverse clinical outcome in many malignancies. This study was aimed to evaluate an immunohistochemical expression status of IMP3 in cutaneous basal cell carcinoma (BCC) and to correlate it with the Ki-67 index values. Methods. Biopsy specimens from 32 cases of BCC were enrolled into this analysis. All samples were immunohistochemically stained for IMP3 (Clone 69.1) and Ki-67 antigen (Clone MIB-1). Results. IMP3 showed a weak expression in 11 (34.4%) cases, a moderate expression in 11 (34.4%) cases, a strong expression in 5 (15.6%) cases, and negative staining in 5 (15.6%) cases. Among seven BCCs exhibiting aggressive-growth features, all but one showed weak reactivity. In contrast, all five BCCs manifesting strong IMP3 positivity consisted of the indolent-growth histologic subtypes. BCCs with infiltrative histomorphology did not appear to have a tendency towards more striking production of IMP3. There was no significant relationship between the IMP3 expression status and the proliferation status (Ki-67 ≤ 50% vs. Ki-67 > 50%) of the tumor tissue (p > 0.05). Conclusions. The vast majority of cutaneous BCCs express IMP3, suggesting this oncoprotein is implicated in BCC carcinogenesis. However, more pronounced expression does not seem to be associated with aggressive-growth phenotype of BCC or higher proliferative activity of neoplastic cells.
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