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本文引用的文献

1
Breast cancer screening among adult women in China, 2010.中国成年女性乳腺癌筛查(2010 年)。
Prev Chronic Dis. 2013 Nov 7;10:E183. doi: 10.5888/pcd10.130136.
2
Mammary carcinoma cell derived cyclooxygenase 2 suppresses tumor immune surveillance by enhancing intratumoral immune checkpoint activity.乳腺癌细胞衍生的环氧化酶2通过增强肿瘤内免疫检查点活性来抑制肿瘤免疫监视。
Breast Cancer Res. 2013;15(5):R75. doi: 10.1186/bcr3469.
3
Up-regulation of PD-L1, IDO, and T(regs) in the melanoma tumor microenvironment is driven by CD8(+) T cells.在黑色素瘤肿瘤微环境中,PD-L1、IDO 和 T(regs)的上调是由 CD8(+) T 细胞驱动的。
Sci Transl Med. 2013 Aug 28;5(200):200ra116. doi: 10.1126/scitranslmed.3006504.
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Survival Advantage in Patients with Metastatic Breast Cancer Receiving Endocrine Therapy plus Sialyl Tn-KLH Vaccine: Post Hoc Analysis of a Large Randomized Trial.内分泌治疗联合唾液酸化 Tn-KLH 疫苗治疗转移性乳腺癌患者的生存优势:一项大型随机试验的事后分析。
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Type III TGF-β receptor downregulation generates an immunotolerant tumor microenvironment.III 型 TGF-β 受体下调可产生免疫耐受的肿瘤微环境。
J Clin Invest. 2013 Sep;123(9):3925-40. doi: 10.1172/JCI65745. Epub 2013 Aug 8.
6
Transcription factor ATF3 links host adaptive response to breast cancer metastasis.转录因子 ATF3 将宿主适应性反应与乳腺癌转移联系起来。
J Clin Invest. 2013 Jul;123(7):2893-906. doi: 10.1172/JCI64410. Epub 2013 Jun 10.
7
Wiskott-Aldrich syndrome protein regulates leukocyte-dependent breast cancer metastasis.Wiskott-Aldrich 综合征蛋白调控白细胞依赖性乳腺癌转移。
Cell Rep. 2013 Aug 15;4(3):429-36. doi: 10.1016/j.celrep.2013.07.007. Epub 2013 Aug 1.
8
MicroRNA-19a-3p inhibits breast cancer progression and metastasis by inducing macrophage polarization through downregulated expression of Fra-1 proto-oncogene.MicroRNA-19a-3p 通过下调 Fra-1 原癌基因的表达诱导巨噬细胞极化,抑制乳腺癌的进展和转移。
Oncogene. 2014 Jun 5;33(23):3014-23. doi: 10.1038/onc.2013.258. Epub 2013 Jul 8.
9
Myeloid-derived suppressor cells in breast cancer.乳腺癌中的髓源抑制细胞。
Breast Cancer Res Treat. 2013 Jul;140(1):13-21. doi: 10.1007/s10549-013-2618-7. Epub 2013 Jul 5.
10
Hydrazinocurcumin Encapsuled nanoparticles "re-educate" tumor-associated macrophages and exhibit anti-tumor effects on breast cancer following STAT3 suppression.载双氢青蒿素姜黄素纳米粒“再教育”肿瘤相关巨噬细胞,并通过抑制 STAT3 发挥抗乳腺癌作用。
PLoS One. 2013 Jun 25;8(6):e65896. doi: 10.1371/journal.pone.0065896. Print 2013.

利用免疫系统治疗乳腺癌。

Harnessing the immune system for the treatment of breast cancer.

机构信息

Department of Medicine, VA Palo Alto Health Care System/Stanford University School of Medicine, Stanford, CA 94305, USA.

出版信息

J Zhejiang Univ Sci B. 2014 Jan;15(1):1-15. doi: 10.1631/jzus.B1300264.

DOI:10.1631/jzus.B1300264
PMID:24390741
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3891115/
Abstract

Standard treatment options for breast cancer include surgery, chemotherapy, radiation, and targeted therapies, such as adjuvant hormonal therapy and monoclonal antibodies. Recently, the recognition that chronic inflammation in the tumor microenvironment promotes tumor growth and survival during different stages of breast cancer development has led to the development of novel immunotherapies. Several immunotherapeutic strategies have been studied both preclinically and clinically and already have been shown to enhance the efficacy of conventional treatment modalities. Therefore, therapies targeting the immune system may represent a promising next-generation approach for the treatment of breast cancers. This review will discuss recent findings that elucidate the roles of suppressive immune cells and proinflammatory cytokines and chemokines in the tumor-promoting microenvironment, and the most current immunotherapeutic strategies in breast cancer.

摘要

乳腺癌的标准治疗选择包括手术、化疗、放疗和靶向治疗,如辅助激素治疗和单克隆抗体。最近,人们认识到肿瘤微环境中的慢性炎症促进了乳腺癌发展的不同阶段的肿瘤生长和存活,这导致了新型免疫疗法的发展。已经有几种免疫治疗策略在临床前和临床研究中进行了研究,并且已经证明它们可以增强常规治疗方法的疗效。因此,靶向免疫系统的治疗方法可能代表了治疗乳腺癌的下一代有前途的方法。这篇综述将讨论最近的发现,这些发现阐明了抑制性免疫细胞和促炎细胞因子和趋化因子在促进肿瘤的微环境中的作用,以及乳腺癌中最新的免疫治疗策略。