Thompson S, Cantwell B M, Cornell C, Turner G A
Department of Clinical Biochemistry, Medical School, Newcastle upon Tyne, UK.
Br J Cancer. 1991 Aug;64(2):386-90. doi: 10.1038/bjc.1991.314.
A previous study has shown that there are high levels of an abnormally-fucosylated form of haptoglobin (FHp) in the blood of cancer patients (Thompson & Turner, 1987b). In this study, we investigated the expression of this substance in serial blood specimens from women with ovarian or breast cancer who were undergoing cytotoxic chemotherapy. The level of FHp was related to patient response to therapy status, this latter index being an indirect determination of tumour burden. FHp levels did not correlate with gross liver metastasis (as shown by CT scans or the blood levels of liver enzymes). This conclusion was further supported by results from patients with hepatocellular cancer. FHp was elevated in most of these patients, but the pattern of change did not correlate with variations in the level of the hepatoma marker, alpha-foetoprotein. It seems likely that FHp is produced by the liver. Primary and secondary tumours could release substances, such as cytokines, which interfere with fucose metabolism in the liver.
先前的一项研究表明,癌症患者血液中存在高水平的异常岩藻糖基化形式的触珠蛋白(FHp)(汤普森和特纳,1987b)。在本研究中,我们调查了接受细胞毒性化疗的卵巢癌或乳腺癌女性患者系列血液标本中这种物质的表达情况。FHp水平与患者对治疗状态的反应相关,后者是肿瘤负荷的间接测定指标。FHp水平与肝脏大转移灶(如CT扫描或肝酶血液水平所示)无关。肝细胞癌患者的结果进一步支持了这一结论。这些患者中的大多数FHp升高,但变化模式与肝癌标志物甲胎蛋白水平的变化无关。FHp似乎是由肝脏产生的。原发性和继发性肿瘤可能释放细胞因子等物质,干扰肝脏中的岩藻糖代谢。