Divisão de Pesquisa Clínica, Instituto Nacional do Câncer - INCA, Rio de Janeiro, RJ, Brasil.
Int Braz J Urol. 2021 Mar-Apr;47(2):295-305. doi: 10.1590/S1677-5538.IBJU.2020.0054.
The standard treatment for locally advanced cervical cancer (CC) is chemo-radiotherapy. Once the bladder receives part of the radiation, a typical inflammatory condition that configures radiation-induced cystitis may develop. Chronic radiation-induced cystitis is commonly characterized by the bladder new submucosal vascularization, which is typically fragile and favors hematuria. The current study aims to investigate if Hypoxia-Induced Factor (HIF-1α) and its transcriptional target Vascular Endothelial Growth Factor A (VEGF-A) could be a primary pathway leading to increased submucosal vascularization. HIF-1α and VEGF-A mRNA levels in bladder core biopsies from CC patients treated with radiotherapy versus untreated (non-irradiated) patients were analyzed using a droplet digital polymerase chain reaction technology. Gene expression results showed that HIF-1α and VEGF-A had no significant differences between bladder samples from patients previously irradiated and untreated patient samples. However, a direct relationship between the degree of late morbidity and the expression of HIF-1α and VEGF-A has been demonstrated. Despite the lack of statistical significance precludes a definitive conclusion, the data presented herein suggests that further studies investigating the role of HIF-1α in bladder neovascularization in radiation-induced cystitis are highly recommended.
局部晚期宫颈癌(CC)的标准治疗方法是化疗放疗。一旦膀胱接受部分辐射,就可能会出现典型的炎症状态,即放射性膀胱炎。慢性放射性膀胱炎的特征通常是膀胱新的黏膜下血管化,通常很脆弱,容易出现血尿。本研究旨在探讨缺氧诱导因子(HIF-1α)及其转录靶标血管内皮生长因子 A(VEGF-A)是否可能是导致黏膜下血管化增加的主要途径。使用液滴数字聚合酶链反应技术分析接受放疗与未接受放疗(未照射)的 CC 患者膀胱核心活检中的 HIF-1α 和 VEGF-A mRNA 水平。基因表达结果表明,先前接受过放疗的患者膀胱样本与未接受治疗的患者膀胱样本中 HIF-1α 和 VEGF-A 无显着差异。然而,已经证明晚期发病率的程度与 HIF-1α 和 VEGF-A 的表达之间存在直接关系。尽管缺乏统计学意义排除了明确的结论,但本文提供的数据表明,强烈建议进一步研究 HIF-1α 在放射性膀胱炎中膀胱新生血管形成中的作用。