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吲哚胺2,3-双加氧酶1通过白细胞介素-6/信号转导及转录激活因子调节乳腺癌对他莫昔芬的耐药性。

Indoleamine 2,3-dioxygenase 1 regulates breast cancer tamoxifen resistance through interleukin-6/signal transducer and activator of transcription.

作者信息

Zhao Xinchun, Jiang Yujia, Xu Ming, Hu Jin, Feng Nan, Deng Huifang, Lu Chong, Huang Tao

机构信息

Department of Breast and Thyroid Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China; Department of General Surgery, First Affiliated Hospital, School of Medicine, Shihezi University, Shihezi, China.

Department of Breast and Thyroid Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Toxicol Appl Pharmacol. 2022 Apr 1;440:115921. doi: 10.1016/j.taap.2022.115921. Epub 2022 Feb 11.

Abstract

Breast cancer is the primary cause of cancer-related deaths in women. Tamoxifen (TAM) is the preferred drug for treating premenopausal luminal-type breast cancer, but TAM resistance restricts its ability to benefit patients. To date, the mechanism of this resistance remains unclear, and there is currently no effective treatment for reversing it. The expression of indoleamine 2,3-dioxygenase 1 (IDO1) has been shown to be elevated in various malignancies. Here, we aimed to investigate the role of IDO1 in TAM-resistant breast cancer. We confirmed that IDO1 is strongly expressed in TAM-resistant breast cancer, and it mediates drug-resistant cell proliferation, metastasis, and TAM resistance in vivo and in vitro through interleukin-6/signal transducer and activator of transcription 3 (IL-6/STAT3). We also found that the mechanism by which TAM upregulates IDO1 is dependent on STAT1 activation. In summary, IDO1 regulates TAM resistance and can serve as a novel target for treatment of TAM-resistant breast cancer.

摘要

乳腺癌是女性癌症相关死亡的主要原因。他莫昔芬(TAM)是治疗绝经前腔面型乳腺癌的首选药物,但他莫昔芬耐药性限制了其使患者受益的能力。迄今为止,这种耐药性的机制仍不清楚,目前尚无有效的逆转治疗方法。吲哚胺2,3-双加氧酶1(IDO1)的表达已被证明在各种恶性肿瘤中升高。在此,我们旨在研究IDO1在他莫昔芬耐药乳腺癌中的作用。我们证实IDO1在他莫昔芬耐药乳腺癌中强烈表达,并且它通过白细胞介素-6/信号转导和转录激活因子3(IL-6/STAT3)在体内和体外介导耐药细胞的增殖、转移和他莫昔芬耐药性。我们还发现他莫昔芬上调IDO1的机制依赖于STAT1激活。总之,IDO1调节他莫昔芬耐药性,可作为治疗他莫昔芬耐药乳腺癌的新靶点。

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