Ayoub Nehad, Alkhatatbeh Mohammad, Jibreel Malak, Ababneh Mera
Department of Clinical Pharmacy, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid 22110, Jordan.
Oncol Lett. 2017 Mar;13(3):1974-1982. doi: 10.3892/ol.2017.5670. Epub 2017 Feb 1.
The development and progression of cancer is a complex and multifactorial process and the global prevalence of obesity is markedly increasing. A number of studies have made an association between obesity and increased rates of epithelial tumors. Obesity is associated with altered adipokine levels, potentially contributing to the process of tumor development and metastasis. In the current study, the associations between circulating adipokines and measures of adiposity and tumor characteristics among patients diagnosed with solid malignancies were examined at the time of presentation, and following the administration of chemotherapy. A total of 30 patients with cancer and matched healthy controls were enrolled in the present study. Plasma adipokine levels of hepatocyte growth factor (HGF), adiponectin and leptin were determined using commercially available ELISA kits. At baseline, plasma HGF, adiponectin and leptin levels were not significantly different between patients with cancer and the healthy controls. Circulating HGF levels were significantly associated with the stage of cancer at diagnosis (P=0.044), but lacked a significant association with lymph node status (P=0.194). Plasma adiponectin and leptin levels were not significantly associated with tumor characteristics at the time of diagnosis. Only leptin was positively correlated with the body mass index of patients with cancer (P<0.001). No significant correlations were detected between the evaluated adipokines and measures of visceral obesity, as determined by waist circumference and the waist-hip ratio at presentation. Following administration of chemotherapy, adiponectin was the only adipokine evaluated in the current study that exhibited a significant difference, when compared with baseline plasma levels (P=0.013), and a significant positive correlation between baseline and follow-up circulating levels (P=0.002) among patients with cancer. In addition, there were no significant inter-correlations between circulating adipokines at baseline level and during follow-up in patients with cancer. Collectively, the findings of the current study suggest a lack of diagnostic roles for the adipokines investigated and no significant association with measures of adiposity. Adiponectin may be a potential adipokine to measure in patients with cancer, in order to further assess its prognostic and predictive potential.
癌症的发生和发展是一个复杂的多因素过程,而全球肥胖患病率正在显著上升。多项研究已将肥胖与上皮肿瘤发病率增加联系起来。肥胖与脂肪因子水平改变有关,这可能促进肿瘤发生和转移过程。在本研究中,对确诊为实体恶性肿瘤的患者在初诊时以及化疗后,检测了循环脂肪因子与肥胖指标及肿瘤特征之间的关联。本研究共纳入了30例癌症患者及匹配的健康对照。使用市售酶联免疫吸附测定(ELISA)试剂盒测定血浆中肝细胞生长因子(HGF)、脂联素和瘦素等脂肪因子水平。基线时,癌症患者与健康对照之间血浆HGF、脂联素和瘦素水平无显著差异。循环HGF水平与诊断时的癌症分期显著相关(P = 0.044),但与淋巴结状态无显著关联(P = 0.194)。诊断时血浆脂联素和瘦素水平与肿瘤特征无显著关联。仅瘦素与癌症患者的体重指数呈正相关(P < 0.001)。初诊时通过腰围和腰臀比确定的评估脂肪因子与内脏肥胖指标之间未检测到显著相关性。化疗后,脂联素是本研究中唯一评估的脂肪因子,与基线血浆水平相比有显著差异(P = 0.013),且癌症患者基线与随访循环水平之间有显著正相关(P = 0.002)。此外,癌症患者基线水平和随访期间循环脂肪因子之间无显著相互关联。总体而言,本研究结果表明所研究的脂肪因子缺乏诊断作用,且与肥胖指标无显著关联。脂联素可能是癌症患者中一种潜在的可测量脂肪因子,以便进一步评估其预后和预测潜力。