Department of Oral Pathology, Federal University of Rio Grande do Norte, Natal, Brazil.
Faculty of Nursing and Medicine Nova Esperança, João Pessoa, Brazil.
Arch Oral Biol. 2022 Apr;136:105387. doi: 10.1016/j.archoralbio.2022.105387. Epub 2022 Feb 22.
To investigate and compare the immunoexpression of E-cadherin, α-SMA, TGF-β and Snail proteins between cases of actinic cheilitis (AC) and squamous cell carcinoma of the lower lip (LLSCC).
E-cadherin, α-SMA, TGF-β and Snail antibody immunostaining was analyzed semiquantitatively in 54 AC cases and in 49 LLSCCs. The cases were classified as low and high expression for analysis of the association with clinicopathological variables and overall survival (OS) and disease-free survival (DFS) rates.
High expression of E-cadherin (cytoplasmic) (p = 0.001) and α-SMA (p < 0.001) was identified in LLSCCs, as well as low expression of TGF-β in LLSCCs (p < 0.001) and high expression of Snail in AC cases (p = 0.006). Survival analysis revealed that high expression of α-SMA at the tumor invasion front, a network immunostaining pattern of this protein, and high expression of TGF-β in tumor buds were significantly associated with poor OS (p < 0.05). There was a higher risk of death among LLSCC cases with high expression of α-SMA (HR = 5.90, p = 0.03). High expression of TGF-β in tumor buds was significantly associated with poor DFS (p = 0.007) and with a higher risk of negative outcomes for DFS (HR = 4.44, p = 0.014).
The present results suggest the potential involvement of dysregulation of proteins associated with epithelial-mesenchymal transition in the modulation of lip carcinogenesis and greater aggressiveness of LLSCC.
研究并比较光化性唇炎(AC)和下唇鳞状细胞癌(LLSCC)病例中 E-钙黏蛋白、α-SMA、TGF-β和 Snail 蛋白的免疫表达。
对半定量分析了 54 例 AC 病例和 49 例 LLSCC 病例中 E-钙黏蛋白、α-SMA、TGF-β和 Snail 抗体的免疫染色。根据与临床病理变量及总生存(OS)和无病生存(DFS)率的相关性,将病例分为低表达和高表达进行分析。
在 LLSCC 中,E-钙黏蛋白(细胞质)(p=0.001)和α-SMA(p<0.001)的高表达,以及 LLSCC 中 TGF-β的低表达(p<0.001)和 AC 病例中 Snail 的高表达(p=0.006)被发现。生存分析显示,肿瘤侵袭前沿α-SMA 的高表达、该蛋白的网络免疫染色模式以及肿瘤芽中 TGF-β的高表达与 OS 不良显著相关(p<0.05)。在 LLSCC 病例中,α-SMA 高表达的死亡风险更高(HR=5.90,p=0.03)。肿瘤芽中 TGF-β的高表达与 DFS 不良显著相关(p=0.007),DFS 不良的风险更高(HR=4.44,p=0.014)。
本研究结果提示,与上皮间质转化相关的蛋白失调可能参与了唇癌的发生和发展,并增加了 LLSCC 的侵袭性。