De Toni Enrico N, Nagel Dorothea, Philipp Alexander B, Herbst Andreas, Thalhammer Isabel, Mayerle Julia, Török Helga-Paula, Brandl Lydia, Kolligs Frank T
Department of Medicine II, University Hospital, LMU Munich, Munich, Germany.
Institute of Laboratory Medicine, University Hospital, LMU Munich, Munich, Germany.
Cell Physiol Biochem. 2018;45(2):605-613. doi: 10.1159/000487101. Epub 2018 Jan 29.
BACKGROUND/AIMS: Osteoprotegerin (OPG) is a soluble receptor of the pro-apoptotic cytokine TRAIL which is thought to contribute to tumour development by inhibiting apoptosis or affecting other aspects of tumour biology, including cell proliferation and immune response. Although immunohistochemical studies suggest that OPG correlates with survival in metastatic colorectal cancer (mCRC), only scarce data are available on serum OPG in CRC patients.
In this pilot study, we assessed the prognostic significance of serum OPG and CEA (Carcinoembryonic antigen) in 81 patients with UICC (Union for International Cancer Control) stage-IV mCRC. OPG was additionally assessed by immunohistochemistry in primary tissue samples from 33 patients of the same cohort.
Baseline serum OPG correlated with CEA (r=0.36, p=0.0011), but independently predicted survival of mCRC patients. Life expectancy was poorer in patients with OPG levels above the median concentration of 51ng/ml (median overall survival [95% confidence interval] 1.8 years [1.3-3.0] vs. 1.0 [0.7-1.2] p=0.013). Patients with high levels of both OPG and CEA had an even poorer life expectancy vs. low-OPG/low-CEA patients (0.9 years [0.6-1.5] vs. 3 years [1.2-4.4], p=0.015), indicating that CEA and OPG have additive prognostic significance. Immunohistochemical analysis of OPG failed to show a correlation between OPG staining and survival (p=0.055) or OPG concentration from matched serum samples.
This pilot study provides evidence of independent prognostic significance of serum OPG in patients with advanced mCRC and warrants its further prospective validation.
背景/目的:骨保护素(OPG)是促凋亡细胞因子TRAIL的可溶性受体,被认为通过抑制凋亡或影响肿瘤生物学的其他方面(包括细胞增殖和免疫反应)来促进肿瘤发展。尽管免疫组化研究表明OPG与转移性结直肠癌(mCRC)的生存率相关,但关于CRC患者血清OPG的资料却很少。
在这项初步研究中,我们评估了81例国际癌症控制联盟(UICC)IV期mCRC患者血清OPG和癌胚抗原(CEA)的预后意义。另外,对同一队列中33例患者的原发组织样本进行了OPG免疫组化分析。
基线血清OPG与CEA相关(r = 0.36,p = 0.0011),但可独立预测mCRC患者的生存率。OPG水平高于中位数浓度51ng/ml的患者预期寿命较差(中位总生存期[95%置信区间]为1.8年[1.3 - 3.0] vs. 1.0[0.7 - 1.2],p = 0.013)。OPG和CEA水平均高的患者与低OPG/低CEA患者相比,预期寿命更差(0.9年[0.6 - 1.5] vs. 3年[1.2 - 4.4],p = 0.015),表明CEA和OPG具有相加的预后意义。OPG免疫组化分析未能显示OPG染色与生存率(p = 0.055)或匹配血清样本中OPG浓度之间的相关性。
这项初步研究提供了血清OPG在晚期mCRC患者中具有独立预后意义的证据,值得进一步进行前瞻性验证。