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胰腺癌相关星状细胞:降低肿瘤微环境中免疫抑制作用的可行靶点。

Pancreatic cancer-associated stellate cells: A viable target for reducing immunosuppression in the tumor microenvironment.

作者信息

Mace Thomas A, Bloomston Mark, Lesinski Gregory B

机构信息

Division of Medical Oncology; Department of Internal Medicine; The Ohio State University; Columbus, OH USA.

出版信息

Oncoimmunology. 2013 Jul 1;2(7):e24891. doi: 10.4161/onci.24891. Epub 2013 May 7.

DOI:10.4161/onci.24891
PMID:24073373
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3782129/
Abstract

Pancreatic cancer-associated stellate cells secrete soluble factors, such as interleukin-6 (IL-6), that promote the accumulation of myeloid-derived suppressor cells via a signal transducer and activator of transcription 3 (STAT3)-dependent mechanism. Targeting components of the IL-6/JAK/STAT3 signaling axis within the tumor stroma could therefore inhibit local immunosuppression and improve the efficacy of immunotherapeutic regimens against pancreatic cancer.

摘要

胰腺癌相关的星状细胞分泌可溶性因子,如白细胞介素-6(IL-6),其通过信号转导和转录激活因子3(STAT3)依赖性机制促进髓源性抑制细胞的积累。因此,靶向肿瘤基质内的IL-6/JAK/STAT3信号轴成分可以抑制局部免疫抑制,并提高针对胰腺癌的免疫治疗方案的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b828/3782129/8e1919358599/onci-2-e24891-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b828/3782129/8e1919358599/onci-2-e24891-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b828/3782129/8e1919358599/onci-2-e24891-g1.jpg

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2
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Antioxid Redox Signal. 2014 Mar 1;20(7):1098-116. doi: 10.1089/ars.2012.5133. Epub 2013 Mar 20.
3
Advances in targeting cell surface signalling molecules for immune modulation.
Cancer Med. 2025 Jun;14(11):e70788. doi: 10.1002/cam4.70788.
4
The Role of Tumor Microenvironment in Pancreatic Cancer Immunotherapy: Current Status and Future Perspectives.肿瘤微环境在胰腺癌免疫治疗中的作用:现状与未来展望。
Int J Mol Sci. 2024 Sep 3;25(17):9555. doi: 10.3390/ijms25179555.
5
Barriers and opportunities in pancreatic cancer immunotherapy.胰腺癌免疫治疗中的障碍与机遇。
NPJ Precis Oncol. 2024 Sep 12;8(1):199. doi: 10.1038/s41698-024-00681-z.
6
Dual roles of myeloid-derived suppressor cells in various diseases: a review.髓系来源抑制性细胞在多种疾病中的双重作用:综述。
Arch Pharm Res. 2024 Jul;47(7):597-616. doi: 10.1007/s12272-024-01504-2. Epub 2024 Jul 15.
7
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9
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10
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5
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6
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J Immunother. 2012 May;35(4):299-308. doi: 10.1097/CJI.0b013e3182518e83.
7
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J Gastroenterol Hepatol. 2012 Mar;27 Suppl 2:69-74. doi: 10.1111/j.1440-1746.2011.07000.x.
8
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10
Pten in stromal fibroblasts suppresses mammary epithelial tumours.基质成纤维细胞中的Pten抑制乳腺上皮肿瘤。
Nature. 2009 Oct 22;461(7267):1084-91. doi: 10.1038/nature08486.