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Regulatory T cells are an important prognostic factor in breast cancer: a systematic review and meta-analysis.调节性 T 细胞是乳腺癌的一个重要预后因素:系统评价和荟萃分析。
Neoplasma. 2016;63(5):789-98. doi: 10.4149/neo_2016_517.
2
Targeting BCL6 and STAT3 in triple negative breast cancer: the one-two punch?针对三阴性乳腺癌中的BCL6和STAT3:组合出击?
Oncoscience. 2015 Nov 21;2(11):912. doi: 10.18632/oncoscience.270. eCollection 2015.
3
International Variation in Female Breast Cancer Incidence and Mortality Rates.女性乳腺癌发病率和死亡率的国际差异。
Cancer Epidemiol Biomarkers Prev. 2015 Oct;24(10):1495-506. doi: 10.1158/1055-9965.EPI-15-0535. Epub 2015 Sep 10.
4
Phagocytes as Corrupted Policemen in Cancer-Related Inflammation.吞噬细胞:癌症相关炎症中的腐败警察。
Adv Cancer Res. 2015;128:141-71. doi: 10.1016/bs.acr.2015.04.013. Epub 2015 Jun 16.
5
Induction of fibronectin by HER2 overexpression triggers adhesion and invasion of breast cancer cells.HER2过表达诱导纤连蛋白触发乳腺癌细胞的黏附和侵袭。
Exp Cell Res. 2015 Apr 10;333(1):116-26. doi: 10.1016/j.yexcr.2015.02.019. Epub 2015 Mar 3.
6
HER2 mediated de novo production of TGFβ leads to SNAIL driven epithelial-to-mesenchymal transition and metastasis of breast cancer.HER2 介导的 TGFβ 的从头合成导致乳腺癌的 SNAIL 驱动的上皮间质转化和转移。
Mol Oncol. 2014 Dec;8(8):1532-47. doi: 10.1016/j.molonc.2014.06.006. Epub 2014 Jun 18.
7
The involvement of JAK-STAT3 in cell motility, invasion, and metastasis.JAK-STAT3在细胞运动、侵袭和转移中的作用。
JAKSTAT. 2014 Jan 1;3(1):e28086. doi: 10.4161/jkst.28086. Epub 2014 Feb 20.
8
The transcriptional modulator BCL6 as a molecular target for breast cancer therapy.转录调节因子BCL6作为乳腺癌治疗的分子靶点。
Oncogene. 2015 Feb 26;34(9):1073-82. doi: 10.1038/onc.2014.61. Epub 2014 Mar 24.
9
β-Catenin promotes colitis and colon cancer through imprinting of proinflammatory properties in T cells.β-连环蛋白通过在 T 细胞中印记促炎特性来促进结肠炎和结肠癌。
Sci Transl Med. 2014 Feb 26;6(225):225ra28. doi: 10.1126/scitranslmed.3007607.
10
Anticancer properties of distinct antimalarial drug classes.不同抗疟药物类别的抗癌特性。
PLoS One. 2013 Dec 31;8(12):e82962. doi: 10.1371/journal.pone.0082962. eCollection 2013.

STAT3 抑制剂氨甲蝶呤在乳腺癌的小鼠模型中显示出抗癌和免疫刺激作用。

The STAT3 inhibitor pyrimethamine displays anti-cancer and immune stimulatory effects in murine models of breast cancer.

机构信息

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.

出版信息

Cancer Immunol Immunother. 2018 Jan;67(1):13-23. doi: 10.1007/s00262-017-2057-0. Epub 2017 Sep 5.

DOI:10.1007/s00262-017-2057-0
PMID:28875329
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5783191/
Abstract

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.

摘要

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。