Department of Biochemistry & Molecular Biology, Tongji Medical College, Huazhong University of Science & Technology, Wuhan 430030, China.
Department of Pathophysiology, Tongji Medical College, Huazhong University of Science & Technology, Wuhan 430030, China.
Cancer Lett. 2015 Aug 10;364(2):118-24. doi: 10.1016/j.canlet.2015.04.030. Epub 2015 May 12.
Lipoxin A4 (LXA4), an arachidonic acid-derived anti-inflammatory lipid mediator, shows anti-tumor potential by regulating tumor immune microenvironments. However, the underlying molecular and cellular basis of this function remains unclear. IL-10-producing B (Breg) cells display tumor-promoting effects by negatively regulating anti-tumor immunity. Here we show that LXA4 inhibits tumor growth by suppressing the generation of Breg cells in tumor-bearing mice. The administration of LXA4 inhibited the induction of Breg cells. Breg cell deficiency, in turn, resulted in LXA4 losing its anti-tumor properties. Intriguingly, regulatory T (Treg) cells also had a role in this process. Targeting Breg cells by LXA4 decreased the number of Treg cells in draining lymph nodes and tumor tissues as well as enhanced cytotoxic T cell activities. In addition, we further demonstrated that LXA4 inhibited Breg cells through its dephosphorylating STAT3 and ERK. These findings unveil a new anti-tumor mechanism underlying LXA4 targeting Breg cells with potential clinical applications.
脂氧素 A4(LXA4)是一种源自花生四烯酸的抗炎脂质介质,通过调节肿瘤免疫微环境显示出抗肿瘤潜力。然而,这种功能的潜在分子和细胞基础尚不清楚。产生白细胞介素 10 的 B(Breg)细胞通过负向调节抗肿瘤免疫而发挥促肿瘤作用。在这里,我们表明 LXA4 通过抑制荷瘤小鼠中 Breg 细胞的生成来抑制肿瘤生长。LXA4 的给药抑制了 Breg 细胞的诱导。反过来,Breg 细胞的缺失导致 LXA4 失去其抗肿瘤特性。有趣的是,调节性 T(Treg)细胞在这个过程中也发挥了作用。通过 LXA4 靶向 Breg 细胞,可减少引流淋巴结和肿瘤组织中 Treg 细胞的数量,并增强细胞毒性 T 细胞的活性。此外,我们还进一步证明,LXA4 通过去磷酸化 STAT3 和 ERK 抑制 Breg 细胞。这些发现揭示了 LXA4 靶向 Breg 细胞的抗肿瘤新机制,具有潜在的临床应用价值。