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丙型肝炎患者血浆中的致断裂因子:它们在肝癌起源中的可能作用。

Clastogenic factors in the plasma of patients with hepatitis C: their possible role at the origin of hepatocarcinoma.

作者信息

Emerit Ingrid, Serejo Fatima, Carneiro de Moura Miguel

机构信息

Institut Biomédical des Cordeliers, University Paris VI, 132 rue Léon Maurice Nordmann, Paris 75013, France.

出版信息

Cancer Genet Cytogenet. 2007 Nov;179(1):31-5. doi: 10.1016/j.cancergencyto.2007.07.012.

Abstract

Clastogenic factors (CF) are endogenous clastogens composed of lipid peroxidation products, cytokines, and abnormal nucleotides of inosine. They are regularly observed after radiation exposure and in chronic inflammatory diseases, where they are supposed to be risk factors for carcinogenesis. In the present study, we evaluate clastogenic activity in the plasma of patients with chronic hepatitis C, HCV-positive liver cirrhosis, and hepatocarcinoma in comparison to liver metastasis. Plasma ultrafiltrates from patients were added to blood cultures of healthy donors (CF test). The chromosomal aberration rates observed in 100 metaphases after 48 hours of cultivation were expressed as adjusted clastogenic scores (ACS). The differences in ACS between the four patient groups and controls were highly significant and represented a 10-fold increase in chromatid-type aberrations. The ACS of patients with cirrhosis and hepatocarcinoma were higher than those of hepatitis patients without these complications, but the differences did not reach statistical significance. Because of cytotoxic effects, the cultures did not grow for 10/17 patients with hepatocarcinoma and were repeated with a reduced volume of ultrafiltrate (0.1 instead of 0.25 mL). The ACS were highest in these 10 patients. When the CF activity of HCV-positive hepatocarcinoma was compared to metastasis because of other malignancies, the differences in ACS were highly significant for the cultures set up with the reduced quantity of ultrafiltrate. The percentage of CF-positive samples was 100% for hepatocarcinoma and 9% for metastasis. The results show that the chromosome-damaging effects of CF increase as the disease progresses to cirrhosis and liver cancer. Formed via the intermediacy of superoxide and generating more superoxide, CF are responsible for an autosustained, long-lived DNA-damaging process, which is documented at the chromosomal level by our technique.

摘要

断裂因子(CF)是由脂质过氧化产物、细胞因子和次黄苷异常核苷酸组成的内源性致断裂剂。在辐射暴露后以及慢性炎症性疾病中经常观察到它们,在这些疾病中它们被认为是致癌的危险因素。在本研究中,我们评估了慢性丙型肝炎、HCV阳性肝硬化和肝癌患者与肝转移患者血浆中的断裂活性。将患者的血浆超滤物添加到健康供体的血液培养物中(CF试验)。培养48小时后在100个中期观察到的染色体畸变率表示为调整后的断裂评分(ACS)。四个患者组与对照组之间的ACS差异非常显著,染色单体型畸变增加了10倍。肝硬化和肝癌患者的ACS高于无这些并发症的肝炎患者,但差异未达到统计学意义。由于细胞毒性作用,17例肝癌患者中有10例培养物未生长,因此用减少体积的超滤物(0.1 mL而不是0.25 mL)重复试验。这10例患者的ACS最高。当将HCV阳性肝癌的CF活性与其他恶性肿瘤引起的转移进行比较时,对于用减少量超滤物建立的培养物,ACS差异非常显著。肝癌CF阳性样本的百分比为100%,转移为9%。结果表明,随着疾病进展为肝硬化和肝癌,CF的染色体损伤作用增强。CF通过超氧化物介导形成并产生更多超氧化物,导致一个自我维持、长期的DNA损伤过程,我们的技术在染色体水平上记录了这一过程。

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