Lissoni P, Rovelli F, Malugani F, Bucovec R, Conti A, Maestroni G J
Division of Radiation Oncology, San Gerardo Hospital, 20052 Monza, Milan, Italy.
Neuro Endocrinol Lett. 2001;22(1):45-7.
The anticancer activity of the indole melatonin has been explained to be due to its immunomodulatory, anti-prolferative and anti-oxidant effects, whereas at present no data are available about its possible influence on the angiogenesis, which has been shown to be one of the main biological mechanisms responsible for tumor dissemination. Vascular endothelial growth factor (VEGF) is the most active angiogenic factor, and the evidence of abnormally high blood levels or VEGF has been proven to be associated with poor prognosis in cancer patients. To investigate the influence of melatonin on angiogenesis, in this preliminary study we have evaluated the effects of melatonin therapy on VEGF blood levels in advanced cancer patients.
MATERIAL & METHODS: The study included 20 metastatic patients, who progressed on previous conventional antitumor therapies and for whom no other effective treatment was available. Melatonin was given orally at 20 mg/day in the evening for at least 2 months. Serum levels of VEGF were measured by an enzyme immunoassay on venous blood samples collected at 15-day intervals.
The clinical response consisted of minor response (MR) in 2, stable disease (SD) in 6 and progressive disease (PD) in the remaining 12 patients. VEGF mean levels decreased on therapy, without, however, statistical differences with respect to the pre-treatment values. In contrast, by evaluating changes in VEGF levels in relation to the clinical response, non-progressing patients (MR + SD) showed a significant decline in VEGF mean concentrations, whereas no effect was achieved in progressing patients.
This study, by showing that melatonin-induced control or the neoplastic growth is associated with a decline in VEGF secretion, would suggest that the pineal hormone may control tumor growth at least in part by acting as a natural anti-angiogenic molecule, with a following opposition or angiogenesis-dependent cancer proliferation.
吲哚类褪黑素的抗癌活性被认为归因于其免疫调节、抗增殖和抗氧化作用,然而目前尚无关于其对血管生成可能影响的数据,而血管生成已被证明是肿瘤扩散的主要生物学机制之一。血管内皮生长因子(VEGF)是最活跃的血管生成因子,血液中VEGF水平异常升高的证据已被证明与癌症患者的不良预后相关。为了研究褪黑素对血管生成的影响,在这项初步研究中,我们评估了褪黑素治疗对晚期癌症患者VEGF血液水平的影响。
该研究纳入了20例转移性患者,这些患者在先前的传统抗肿瘤治疗中病情进展,且没有其他有效的治疗方法。褪黑素于晚上口服,剂量为20mg/天,至少服用2个月。通过酶免疫测定法对每隔15天采集的静脉血样本测量VEGF的血清水平。
临床反应包括2例轻微反应(MR)、6例病情稳定(SD)和其余12例病情进展(PD)。治疗期间VEGF平均水平下降,但与治疗前值相比无统计学差异。相比之下,通过评估VEGF水平相对于临床反应的变化,病情未进展的患者(MR + SD)VEGF平均浓度显著下降,而病情进展的患者未出现效果。
本研究表明,褪黑素诱导的肿瘤生长控制与VEGF分泌下降有关,这表明松果体激素可能至少部分通过作为一种天然抗血管生成分子发挥作用来控制肿瘤生长,进而对抗血管生成依赖性的癌症增殖。