Angiodrastic Chemokines Production by Colonic Cancer Cell Lines

Onco Pub Date : 2022-04-29 DOI:10.3390/onco2020006
Emmanouil George, Moursellas Andrew, Tzardi Maria, Voumvouraki Argyro, Kouroumalis Elias
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引用次数: 1

Abstract

Purpose: To study the production of angiodrastic chemokines by colonic cancer cell lines. Methods: A pro-angiogenic factor (VEGF), two angiogenic chemokines (CXCL8, CXCL6), and one angiostatic (CXCL4) chemokine were measured by ELISA in the supernatants of the colon cancer cell lines HT-29 and Caco-2. Cells were cultured for 24 h in the presence of serum from cancer patients or healthy individuals. Results were analyzed by one-way ANOVA and the General Linear Model for repeated measures. Results: Colonic epithelial cells are potent producers of angiodrastic chemokines. HT-29 and Caco-2 cells produce all four chemokines under basal conditions and 24 h after incubation with human serum. The secretion response, however, was completely different. HT-29 cells produce more CXCL8 and VEGF irrespective of culture conditions, while Caco-2 cells seem unresponsive with respect to CXCL6 and CXCL4. Moreover, HT-29 cells produce more CXCL8 and VEGF when incubated with cancer serum, contrary to Caco-2 cells which produce more CXCL4 under the same conditions. Conclusions: The two colon cancer cell lines were producers of all chemokines studied, but their responses were not uniform under similar culture conditions. CXCL8 and VEGF are differently regulated compared to CXCL4 and CXCL6 in these two cell lines
结肠癌细胞系血管趋化因子的产生
目的:研究结肠癌癌症细胞系分泌血管紧张性趋化因子的情况。方法:用ELISA法检测癌症细胞株HT-29和Caco-2的上清液中一种促血管生成因子(VEGF)、两种血管生成趋化因子(CXCL8、CXCL6)和一种血管生成性趋化因子。细胞在癌症患者或健康个体的血清存在下培养24小时。结果通过单因素方差分析和重复测量的一般线性模型进行分析。结果:结肠上皮细胞是血管紧张性趋化因子的有效生产者。HT-29和Caco-2细胞在基础条件下和与人血清孵育24小时后产生所有四种趋化因子。然而,分泌反应却完全不同。无论培养条件如何,HT-29细胞都会产生更多的CXCL8和VEGF,而Caco-2细胞似乎对CXCL6和CXCL4没有反应。此外,当与癌症血清孵育时,HT-29细胞产生更多的CXCL8和VEGF,这与在相同条件下产生更多CXCL4的Caco-2细胞相反。结论:癌症细胞系是所研究的所有趋化因子的产生者,但在相似的培养条件下,它们的反应并不一致。在这两种细胞系中,CXCL8和VEGF与CXCL4和CXCL6相比受到不同的调节
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