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Interleukin-22 promotes aerobic glycolysis associated with tumor progression via targeting hexokinase-2 in human colon cancer cells

机译:白介素-22通过靶向人类结肠癌细胞中的己糖激酶-2促进与肿瘤进展相关的有氧糖酵解

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摘要

Interleukin-22 has been explored extensively in human cancer, but its functions and underlying mechanisms are incompletely understood. Here, we show that aberrant interleukin-22 expression facilitates aerobic glycolysis in colon cancer cells. Elevated interleukin-22 mRNA expression was observed and positively correlated with hexokinase-2 in colon cancer tissues. In vitro, interleukin-22 enhanced glucose consumption and lactate production via targeting hexokinase-2 in colon cancer cells. Moreover, the transcriptional factor c-Myc and signal transducer and activator of transcription 3 were involved in interleukin-22-induced up-regulation of hexokinase-2. We further demonstrated that hexokinase-2 partly accounted for interleukin-22-mediated cellular proliferation in DLD-1 cells. In vivo, our data demonstrated that interleukin-22 significantly promoted tumor growth along with elevated expression of c-Myc and hexokinase-2 in mice. In summary, our findings provide a new perspective on the pro-inflammatory cytokine interleukin-22 in promoting aerobic glycolysis associated with tumor progression in human colon cancer cells.
机译:白介素-22在人类癌症中已被广泛研究,但其功能和潜在机制尚不完全清楚。在这里,我们显示异常的白介素22表达促进结肠癌细胞中的有氧糖酵解。在结肠癌组织中观察到白介素-22 mRNA表达升高,并与己糖激酶-2呈正相关。在体外,白介素22通过靶向结肠癌细胞中的己糖激酶-2来提高葡萄糖消耗和乳酸的产生。此外,转录因子c-Myc和信号转导和转录激活因子3参与白介素22诱导的己糖激酶-2的上调。我们进一步证明,己糖激酶2部分解释了DLD-1细胞中白介素22介导的细胞增殖。在体内,我们的数据表明白介素22显着促进了小鼠肿瘤的生长以及c-Myc和hexokinase-2表达的升高。总之,我们的发现为促炎性细胞因子白介素-22在促进人类结肠癌细胞中与肿瘤进展相关的需氧糖酵解中提供了新的视角。

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