Xu Heng, Wu Jianzhong, Chen Bo, Li Meng, Tian Yanna, He Mingfang, Xue Jing, Wang Jiangnan, Bai Shan, Sharma Ashok, Liu Haitao, Tang Jinhai, She Jin-Xiong
Institute of Translational Medicine, School of Pharmaceutical Sciences, Nanjing Tech University Nanjing, Jiangsu Province, 210009, China.
Jiangsu Cancer Hospital, Nanjing Medical University Nanjing, Jiangsu, 210009, China.
Am J Transl Res. 2014 Nov 22;6(6):850-6. eCollection 2014.
DKK1 is a secreted glycoprotein that inhibits Wnt/β-catenin signaling but may up-regulate the nonconanical Wnt signaling. Consistent with its inhibitory function in Wnt/β-catenin signaling, aberrant DKK1 expression has been observed in many types of human cancers, while contradicting findings have been reported in other studies. There are also several studies on serum DKK1 levels in various cancers with conflicting findings. In the present study, serum DKK1 was determined in 217 non- small cell lung cancer (NSCLC) patients, 35 small cell lung cancer (SCLC) patients and 286 matched healthy controls using a commercially available ELISA assay kit. Compared to healthy controls, serum DKK1 level was significantly lower in NSCLC (p < 10(-28)) and SCLC (p <10(-4)) patients. Interestingly, serum DKK1 level was higher in NSCLC patients in stage IV (p < 0.0005), with lymph node involvement (p < 0.0002) or with metastasis (p < 0.0001), suggesting that DKK1 may promote metastasis. After surgery and/or chemotherapy, serum DKK1 level is rapidly increased and reached levels observed in healthy controls in most patients. The degree of post therapeutic DKK1 increase varied in different treatment regimens. Our results thus provide strong evidence for the reduced levels of serum DKK1 in both types of lung cancer. However, in the context of all published studies, DKK1 appears to have a dichotomous role in cancer and its effect in a given cancer type or even a given cancer patient is likely to depend on the molecular context of the patient.
DKK1是一种分泌型糖蛋白,它抑制Wnt/β-连环蛋白信号通路,但可能上调非经典Wnt信号通路。与其在Wnt/β-连环蛋白信号通路中的抑制功能一致,在许多类型的人类癌症中都观察到了异常的DKK1表达,而其他研究则报道了相互矛盾的结果。关于各种癌症患者血清DKK1水平也有几项研究,结果相互矛盾。在本研究中,使用市售的ELISA检测试剂盒测定了217例非小细胞肺癌(NSCLC)患者、35例小细胞肺癌(SCLC)患者和286例匹配的健康对照者的血清DKK1。与健康对照相比,NSCLC患者(p < 10(-28))和SCLC患者(p < 10(-4))的血清DKK1水平显著降低。有趣的是,IV期NSCLC患者(p < 0.0005)、有淋巴结转移(p < 0.0002)或有远处转移(p < 0.0001)的患者血清DKK1水平较高,这表明DKK1可能促进转移。手术和/或化疗后,大多数患者的血清DKK1水平迅速升高并达到健康对照者的水平。不同治疗方案后DKK1升高的程度有所不同。因此,我们的结果为两种类型肺癌患者血清DKK1水平降低提供了有力证据。然而,在所有已发表的研究背景下,DKK1在癌症中似乎具有双重作用,其在特定癌症类型甚至特定癌症患者中的作用可能取决于患者的分子背景。