Väyrynen Juha P, Kantola Tiina, Väyrynen Sara A, Klintrup Kai, Bloigu Risto, Karhu Toni, Mäkelä Jyrki, Herzig Karl-Heinz, Karttunen Tuomo J, Tuomisto Anne, Mäkinen Markus J
Cancer and Translational Medicine Research Unit, University of Oulu, Oulu, Finland.
Department of Pathology, Oulu University Hospital and Medical Research Center Oulu, Oulu, Finland.
Int J Cancer. 2016 Jul 1;139(1):112-21. doi: 10.1002/ijc.30040. Epub 2016 Mar 7.
Increased inflammatory cell infiltration correlates to improved survival in colorectal cancer (CRC). Development and progression of CRC is associated with alterations in serum cytokine levels but their significance is not well defined. In this study, we investigated the relationships between the serum levels of 13 cytokines and the densities of eight types of tumor infiltrating inflammatory cells and their impact on disease-free survival (DFS), cancer-specific survival (CSS) and overall survival (OS) in a prospectively recruited group of 147 CRC patients. There were strong positive correlations between the serum concentrations of different cytokines, as well as between the different types of tumor infiltrating immune cells, whereas the associations between serum cytokines and tumor infiltrating immune cells were generally weak. High serum IL-12 levels associated with increased densities of peritumoral CD8(+) T cells, intraepithelial CD3(+) T cells and intratumoral neutrophils, while high serum CCL4 levels associated with increased densities of peritumoral CD68(+) cells. In multivariate survival models, increased infiltration of intraepithelial CD3(+) T cells and increased serum CCL4 associated with improved DFS, whereas higher intratumoral CD83(+) dendritic cell density and increased serum interferon gamma levels associated with improved CSS and OS. Also high density of peritumoral CD3(+) T cells associated with improved CSS. In conclusion, serum cytokines and tumor infiltrating immune cells in CRC represent entities with high intragroup correlations but relatively weak intergroup correlations. The results suggest that tumor infiltrating CD3(+) T cells, CD83(+) dendritic cells, serum CCL4 and serum interferon gamma represent relevant markers of disease outcome.
炎症细胞浸润增加与结直肠癌(CRC)患者生存率提高相关。CRC的发生和进展与血清细胞因子水平的改变有关,但其意义尚未明确界定。在本研究中,我们调查了147例前瞻性招募的CRC患者血清中13种细胞因子水平与8种肿瘤浸润性炎症细胞密度之间的关系,以及它们对无病生存期(DFS)、癌症特异性生存期(CSS)和总生存期(OS)的影响。不同细胞因子的血清浓度之间,以及不同类型的肿瘤浸润免疫细胞之间存在强正相关,而血清细胞因子与肿瘤浸润免疫细胞之间的关联通常较弱。血清IL-12水平高与瘤周CD8(+) T细胞、上皮内CD3(+) T细胞和瘤内中性粒细胞密度增加相关,而血清CCL4水平高与瘤周CD68(+)细胞密度增加相关。在多变量生存模型中,上皮内CD3(+) T细胞浸润增加和血清CCL4增加与DFS改善相关,而瘤内CD83(+)树突状细胞密度较高和血清干扰素γ水平增加与CSS和OS改善相关。瘤周CD3(+) T细胞高密度也与CSS改善相关。总之,CRC中的血清细胞因子和肿瘤浸润免疫细胞代表组内相关性高但组间相关性相对较弱的实体。结果表明,肿瘤浸润性CD3(+) T细胞、CD83(+)树突状细胞、血清CCL4和血清干扰素γ是疾病预后的相关标志物。