Orthopaedic Surgery and Traumatology Department, Clínica San Miguel, Beloso Alto 36, 31006 Pamplona, Spain.
DISIT Biotech, Fuenlabrada Hospital, 28942 Madrid, Spain.
Curr Oncol. 2022 Apr 12;29(4):2650-2661. doi: 10.3390/curroncol29040217.
Radiation-induced fibrosis (RIF) is a severe side effect related with soft tissues sarcomas (STS) radiotherapy. RIF is a multicellular process initiated primarily by TGF-β1 that is increased in irradiated tissue, whose signaling leads to intracellular Smad2/3 phosphorylation and further induction of profibrotic target genes. P144 (Disetertide©) is a peptide inhibitor of TGF-β1 and is proposed as a candidate compound for reducing RIF associated wound healing problems and muscle fibrosis in STS.
A treatment and control group of WNZ rabbits were employed to implement a brachytherapy animal model, through catheter implantation at the lower limb. Two days after implantation, animals received 20 Gy isodosis, intended to induce a high RIF grade. The treatment group received intravenous P144 administration following a brachytherapy session, repeated at 24-72 h post-radiation, while the control group received placebo. Four weeks later, affected muscular tissues underwent histological processing for collagen quantification and P-Smad2/3 immunohistochemistry through image analysis.
High isodosis Brachytherapy produced remarkable fibrosis in this experimental model. Results showed retained macro and microscopical morphology of muscle in the P144 treated group, with reduced extracellular matrix fibrosis, with a lower area of collagen deposition measured through Masson's trichrome staining. Intravenous P144 also induced a significant reduction in Smad2/3 phosphorylation levels compared with the placebo group.
P144 administration clearly reduces RIF and opens a new potential co-treatment approach to reduce complications in soft tissue sarcoma (STS) radiotherapy. Further studies are required to establish whether the dosage and timing optimization of P144 administration, in different RIF phases, might entirely avoid fibrosis associated with STS brachytherapy.
辐射诱导纤维化(RIF)是软组织肉瘤(STS)放射治疗的一种严重副作用。RIF 是一种多细胞过程,主要由 TGF-β1 引发,在辐照组织中增加,其信号导致细胞内 Smad2/3 磷酸化,进一步诱导促纤维化靶基因。P144(Disetertide©)是 TGF-β1 的肽抑制剂,被提议作为一种候选化合物,用于减少与 STS 相关的 RIF 引起的伤口愈合问题和肌肉纤维化。
WNZ 兔的治疗组和对照组被用来实施近距离放射治疗动物模型,通过在下肢植入导管。植入后两天,动物接受 20Gy 等剂量照射,旨在诱导高 RIF 级。治疗组在放射治疗后 24-72 小时接受静脉内 P144 给药,而对照组接受安慰剂。四周后,受影响的肌肉组织接受胶原定量的组织学处理,并通过图像分析进行 P-Smad2/3 免疫组织化学。
高剂量近距离放射治疗在该实验模型中产生了显著的纤维化。结果表明,在 P144 治疗组中保留了肌肉的宏观和微观形态,细胞外基质纤维化减少,通过 Masson 三色染色测量的胶原沉积面积较低。与安慰剂组相比,静脉内 P144 还诱导了 Smad2/3 磷酸化水平的显著降低。
P144 给药明显减轻了 RIF,并为减少软组织肉瘤(STS)放射治疗的并发症开辟了新的潜在联合治疗方法。需要进一步研究以确定 P144 给药的剂量和时间优化,在不同的 RIF 阶段,是否可以完全避免与 STS 近距离放射治疗相关的纤维化。