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卵巢肿瘤微环境中的免疫细胞群体

Immune Cell Population in Ovarian Tumor Microenvironment.

作者信息

Cai Dong Li, Jin Li-Ping

机构信息

Clinical and Translational Research Center, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, Shanghai 201204, China.

Laboratory for Reproductive Immunology, Hospital of Obstetrics and Gynecology, Fudan University Shanghai Medical College, Shanghai 200011, China.

出版信息

J Cancer. 2017 Aug 25;8(15):2915-2923. doi: 10.7150/jca.20314. eCollection 2017.

DOI:10.7150/jca.20314
PMID:28928882
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5604442/
Abstract

Ovarian cancer, the third most common with highest mortality rates gynecological malignancy among women in China, is characterized by a unique tumor immune microenvironment. Immune-cell population infiltrated into the tumor tissue among patients with ovarian cancer are associated positively or negatively with antitumor activity. The imbalance between immune activation and immune suppression can result in oncogenesis and cancer progression. Therefore, intense investigation of the immunologic mechanism of ovarian cancer is urgently needed, and a comprehensive understanding of the network in which immune cells interact with the microenvironment, tumor cells and each other will greatly promote the development of more effective immunotherapies for ovarian cancer. In this review, we will focus on the main immune-cell population in ovarian tumor microenvironment, discuss their role in tumor progression and try to give the readers a new perspective in finding more promising therapeutic targets for cancers.

摘要

卵巢癌是中国女性中第三常见且死亡率最高的妇科恶性肿瘤,其特征在于独特的肿瘤免疫微环境。浸润到卵巢癌患者肿瘤组织中的免疫细胞群体与抗肿瘤活性呈正相关或负相关。免疫激活与免疫抑制之间的失衡可导致肿瘤发生和癌症进展。因此,迫切需要深入研究卵巢癌的免疫机制,全面了解免疫细胞与微环境、肿瘤细胞以及彼此之间相互作用的网络,这将极大地促进针对卵巢癌更有效免疫疗法的发展。在本综述中,我们将聚焦于卵巢肿瘤微环境中的主要免疫细胞群体,讨论它们在肿瘤进展中的作用,并试图为读者提供一个新的视角,以寻找更有前景的癌症治疗靶点。

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Immune Cell Population in Ovarian Tumor Microenvironment.卵巢肿瘤微环境中的免疫细胞群体
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Integrated multi-omics analysis reveals the immunotherapeutic significance of tumor cells with high FN1 expression in ovarian cancer.整合多组学分析揭示了 FN1 高表达肿瘤细胞在卵巢癌中的免疫治疗意义。
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本文引用的文献

1
Clinical Use of Programmed Cell Death-1 and Its Ligand Expression as Discriminatory and Predictive Markers in Ovarian Cancer.程序性细胞死亡受体 1 及其配体表达在卵巢癌中的鉴别和预测标志物的临床应用。
Clin Cancer Res. 2017 Jul 1;23(13):3453-3460. doi: 10.1158/1078-0432.CCR-16-2366. Epub 2016 Dec 16.
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Tumor-associated macrophages drive spheroid formation during early transcoelomic metastasis of ovarian cancer.肿瘤相关巨噬细胞在卵巢癌早期经体腔转移过程中驱动球体形成。
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4
CD103+ intraepithelial T cells in high-grade serous ovarian cancer are phenotypically diverse TCRαβ+ CD8αβ+ T cells that can be targeted for cancer immunotherapy.高级别浆液性卵巢癌中的CD103⁺上皮内T细胞是表型多样的TCRαβ⁺CD8αβ⁺T细胞,可成为癌症免疫治疗的靶点。
Oncotarget. 2016 Nov 15;7(46):75130-75144. doi: 10.18632/oncotarget.12077.
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CCL18 from ascites promotes ovarian cancer cell migration through proline-rich tyrosine kinase 2 signaling.腹水中的CCL18通过富含脯氨酸的酪氨酸激酶2信号通路促进卵巢癌细胞迁移。
Mol Cancer. 2016 Sep 9;15(1):58. doi: 10.1186/s12943-016-0542-2.
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MAbs. 2016 Nov/Dec;8(8):1437-1455. doi: 10.1080/19420862.2016.1219005. Epub 2016 Aug 5.
7
Expression of Vascular Endothelial Growth Factor in Ovarian Cancer Inhibits Tumor Immunity through the Accumulation of Myeloid-Derived Suppressor Cells.血管内皮生长因子在卵巢癌中的表达通过髓系来源的抑制细胞的积累抑制肿瘤免疫。
Clin Cancer Res. 2017 Jan 15;23(2):587-599. doi: 10.1158/1078-0432.CCR-16-0387. Epub 2016 Jul 11.
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Epithelial ovarian cancer-secreted exosomal miR-222-3p induces polarization of tumor-associated macrophages.上皮性卵巢癌分泌的外泌体 miR-222-3p 诱导肿瘤相关巨噬细胞极化。
Oncotarget. 2016 Jul 12;7(28):43076-43087. doi: 10.18632/oncotarget.9246.
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How Ovarian Cancer Evades Immune Scrutiny.卵巢癌如何逃避免疫监测。
Cancer Discov. 2016 Apr;6(4):OF1. doi: 10.1158/2159-8290.CD-NB2016-026. Epub 2016 Mar 8.
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Combined Immunoscore of CD103 and CD3 Identifies Long-Term Survivors in High-Grade Serous Ovarian Cancer.CD103和CD3联合免疫评分可识别高级别浆液性卵巢癌的长期存活者。
Int J Gynecol Cancer. 2016 May;26(4):671-9. doi: 10.1097/IGC.0000000000000672.