Canney P A, Dean S
Wessex Regional Radiotherapy Centre, Southampton.
Br J Radiol. 1990 Aug;63(752):620-3. doi: 10.1259/0007-1285-63-752-620.
Transforming growth factor beta (TGF-beta) is a peptide which has a fundamental role in controlling proliferation of many cell types. Its main effect upon connective tissues in vivo is to stimulate growth. It can result in endothelial cell proliferation but tends to inhibit epithelial cell growth. Damage to the connective tissues and the vasculature are the principal findings in late radiotherapy damage. Following the initial cellular depletion after radiotherapy, an abnormal proliferation of these tissues occurs, which does not respond to normal feedback mechanisms. Immunocytochemical staining for TGF-beta has been performed upon six patients who had received pre-operative radiotherapy and three patients who had surgery alone for large bowel tumours. Transforming growth factor beta was found in relation to the pathological changes of late radiation damage in the non-tumour-bearing tissues of four out of six previously irradiated patients, but in none of the non-irradiated patients. This paper proposes that TGF-beta activity may modulate late post-radiation changes.
转化生长因子β(TGF-β)是一种在控制多种细胞类型增殖方面具有重要作用的肽。它在体内对结缔组织的主要作用是刺激生长。它可导致内皮细胞增殖,但往往抑制上皮细胞生长。结缔组织和脉管系统的损伤是放射治疗晚期损伤的主要表现。放疗后最初细胞减少后,这些组织会出现异常增殖,且对正常反馈机制无反应。对6例接受术前放疗的患者和3例仅接受手术治疗的大肠肿瘤患者进行了TGF-β免疫细胞化学染色。在6例先前接受放疗的患者中,有4例的非肿瘤组织中发现了与放射治疗晚期损伤病理变化相关的转化生长因子β,而在未接受放疗的患者中均未发现。本文提出TGF-β活性可能调节放疗后的晚期变化。