Department of Molecular Medicine and Surgery, Section of Reconstructive Plastic Surgery, Karolinska Institutet, Stockholm, Sweden.
J Plast Reconstr Aesthet Surg. 2010 Nov;63(11):1910-6. doi: 10.1016/j.bjps.2009.12.001. Epub 2010 Jan 15.
Surgical wounds within previously irradiated tissues are common in reconstructive surgery and subject to an increased incidence of postoperative complications due to vascular dysfunction, including thrombosis in both microvascular anastomosis and the microcirculatory bed. However, there is no study that has described gene expression patterns in radiated human blood vessels. This study aims to determine if radiation can induce changes in gene expression that can promote thrombus formation in human microvascular recipient veins.
Paired biopsies from radiated recipient veins and non-radiated flap veins were simultaneously harvested from 15 patients during free-flap reconstruction, 4-215 weeks from termination of radiation. Radiated and non-radiated veins were compared using a custom-made Taqman(®) low-density array (TLDA) to analyse differential gene expression in a large number of genes involved in inflammation and coagulation. Results were confirmed by real-time polymerase chain reaction (RT-PCR) and immunohistochemistry.
Results from TLDA indicate an acute increase of cytokines and leucocyte adhesion molecules related to activation of transcription factor nuclear factor kappa-B (NF-kB), confined to the first 3 months after radiotherapy treatment. Results were confirmed by RT-PCR and activity localised to the endothelium by immunohistochemistry. RT-PCR analyses of genes associated with coagulation showed sustained expression of plasminogen activator inhibitor-1 (PAI-1) in radiated veins.
We found an acute inflammatory response with endothelial activation, followed by a sustained PAI-1 gene expression in irradiated microvascular recipient veins that can explain adverse effects years after radiation, such as microvascular occlusion and poor surgical wound healing. We believe that the results contribute to the search for therapeutic adjuncts to cope with the adverse effects of radiation therapy and strongly advocate postoperative, rather than preoperative, radiotherapy whenever possible.
在重建手术中,先前接受过放射治疗的组织中的手术伤口很常见,由于血管功能障碍,包括微血管吻合术和微循环床中的血栓形成,术后并发症的发生率增加。然而,尚无研究描述过放射后的人血管中的基因表达模式。本研究旨在确定放射是否会引起基因表达的变化,从而促进人微血管受体静脉中的血栓形成。
在游离皮瓣重建期间,从 15 名患者中同时采集受照射受体静脉和未受照射皮瓣静脉的配对活检样本,距放射治疗结束后 4-215 周。使用定制的 Taqman(®)低密度阵列(TLDA)比较受照射和未受照射的静脉,以分析大量涉及炎症和凝血的基因的差异表达。通过实时聚合酶链反应(RT-PCR)和免疫组织化学证实了结果。
TLDA 的结果表明,转录因子核因子 kappa-B(NF-kB)的激活相关的细胞因子和白细胞黏附分子在放射治疗后 3 个月内急性增加,仅限于此。通过 RT-PCR 和免疫组织化学将活性定位于内皮证实了这一点。与凝血相关的基因的 RT-PCR 分析显示,放射血管中纤溶酶原激活物抑制剂-1(PAI-1)的持续表达。
我们发现受照射的微血管受体静脉中存在急性炎症反应和内皮细胞激活,随后持续表达 PAI-1 基因,这可以解释放射治疗多年后的不良影响,如微血管闭塞和手术伤口愈合不良。我们认为,这些结果有助于寻找治疗辅助手段来应对放射治疗的不良影响,并强烈主张在可能的情况下,术后而不是术前进行放射治疗。