Papadakos Konstantinos S, Darlix Amélie, Jacot William, Blom Anna M
Division of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö, Sweden.
Department of Medical Oncology, Institut Régional du Cancer Montpellier ICM, University of Montpellier, Montpellier, France.
Front Oncol. 2019 Oct 30;9:1141. doi: 10.3389/fonc.2019.01141. eCollection 2019.
Cartilage oligomeric matrix protein (COMP) is a pentameric cartilage protein also expressed in breast cancer tumors. A high expression of COMP evaluated by immunohistochemical staining is as an independent prognostic marker associated with poor patients' prognosis. Herein, levels of COMP were analyzed using an IVD approved ELISA in serum samples from 233 well-characterized breast cancer patients; 176 with metastatic breast cancer; and 57 in an early stage of the disease. The metastatic patients had double the concentration of serum COMP compared with those with early breast cancer. High levels of COMP in sera of metastatic patients were associated with the histological subtype ( = 0.025) and estrogen receptor positivity ( = 0.019) at the time of breast cancer diagnosis. Further, correlation was observed between the serum levels of COMP and the presence of liver ( = 0.010) or bone ( = 0.010) metastases in this population. Most importantly, elevated serum levels of COMP appear to serve as an independent prognostic marker of survival as assessed by Cox proportional hazard regression analysis ( = 0.001) for the metastatic patients. Among metastatic patients treated with taxanes (Docetaxel-Paclitaxel) as part of their first metastatic line ( = 25), those with high levels of serum COMP detected in the metastatic stage of the disease had a shorter median survival (0.2 years) compared with those with low levels of serum COMP (1.1 years) ( = 0.001). Taken together, the serum levels of COMP are elevated in the metastatic patients and may be a potential novel biomarker for the evaluation of the prognosis in this population.
软骨寡聚基质蛋白(COMP)是一种五聚体软骨蛋白,在乳腺癌肿瘤中也有表达。通过免疫组织化学染色评估的COMP高表达是与患者预后不良相关的独立预后标志物。在此,使用经体外诊断试剂批准的酶联免疫吸附测定(ELISA)分析了233例特征明确的乳腺癌患者血清样本中COMP的水平;其中176例为转移性乳腺癌患者;57例处于疾病早期。转移性患者血清COMP浓度是早期乳腺癌患者的两倍。转移性患者血清中高水平的COMP与乳腺癌诊断时的组织学亚型(P = 0.025)和雌激素受体阳性(P = 0.019)相关。此外,在该人群中观察到COMP血清水平与肝转移(P = 0.010)或骨转移(P = 0.010)的存在之间存在相关性。最重要的是,通过Cox比例风险回归分析评估(P = 0.001),转移性患者血清COMP水平升高似乎是生存的独立预后标志物。在作为一线转移性治疗(n = 25)接受紫杉烷类(多西他赛 - 紫杉醇)治疗的转移性患者中,疾病转移阶段检测到血清COMP水平高的患者中位生存期(0.2年)比血清COMP水平低的患者(1.1年)短(P = 0.001)。综上所述,转移性患者血清COMP水平升高,可能是评估该人群预后的潜在新型生物标志物。