Department of Biology, San Diego State University, 5500 Campanile Drive, NLS-407, San Diego, CA, 92182, USA.
Department of Immunology, Department of Surgery, Mayo Clinic, Guggenheim 3-42B, Rochester, MN, 55905, USA.
Cancer Immunol Immunother. 2018 Jan;67(1):13-23. doi: 10.1007/s00262-017-2057-0. Epub 2017 Sep 5.
The transcription factor signal activator and transducer or transcription (STAT3), which regulates genes controlling proliferation, survival, and invasion, is activated inappropriately in many human cancers, including breast cancer. Activation of STAT3 can lead to both malignant cellular behavior and suppression of immune cell function in the tumor microenvironment. Through a chemical-biology screen, pyrimethamine (PYR), an FDA approved anti-microbial drug, was identified as an inhibitor of STAT3 function at concentrations known to be achieved safely in humans. We report that PYR shows therapeutic activity in two independent mouse models of breast cancer, with both direct tumor inhibitory and immune stimulatory effects. PYR-inhibited STAT3 activity in TUBO and TM40D-MB metastatic breast cancer cells in vitro and inhibited tumor cell proliferation and invasion into Matrigel basement membrane matrix. In tumor-transplanted mice, PYR had both direct and indirect tumor inhibitory effects. Tumor-bearing mice treated with PYR showed reduced STAT3 activation in tumor cells, attenuated tumor growth, and reduced tumor-associated inflammation. In addition, expression of Lamp1 by tumor infiltrating CD8 T cells was elevated, indicating enhanced release of cytotoxic granules. These findings suggest that PYR may have beneficial effects in the treatment of breast cancer.
转录因子信号激活物和转导子或转录(STAT3)调节控制增殖、存活和侵袭的基因,在许多人类癌症中(包括乳腺癌)不适当激活。STAT3 的激活可导致肿瘤微环境中的恶性细胞行为和免疫细胞功能抑制。通过化学生物学筛选,发现苯巴比妥(PYR),一种美国食品和药物管理局批准的抗微生物药物,在已知可在人体内安全达到的浓度下,可作为 STAT3 功能的抑制剂。我们报告称,PYR 在两种独立的乳腺癌小鼠模型中具有治疗活性,具有直接的肿瘤抑制和免疫刺激作用。PYR 在体外抑制 TUBO 和 TM40D-MB 转移性乳腺癌细胞中的 STAT3 活性,并抑制肿瘤细胞增殖和侵袭 Matrigel 基底膜基质。在荷瘤小鼠中,PYR 具有直接和间接的肿瘤抑制作用。用 PYR 治疗的荷瘤小鼠显示肿瘤细胞中 STAT3 激活减少,肿瘤生长减弱,肿瘤相关炎症减少。此外,肿瘤浸润性 CD8 T 细胞中 Lamp1 的表达升高,表明细胞毒性颗粒的释放增强。这些发现表明 PYR 可能对乳腺癌的治疗有有益的作用。