Suppr超能文献

分析导管原位癌肿瘤微环境中的基质特征。

Analysis of stromal signatures in the tumor microenvironment of ductal carcinoma in situ.

机构信息

Department of Pathology, Stanford University Hospital, Room L235, 300 Pasteur Drive, Stanford, CA 94305, USA.

出版信息

Breast Cancer Res Treat. 2010 Sep;123(2):397-404. doi: 10.1007/s10549-009-0654-0. Epub 2009 Dec 1.

Abstract

Recent advances in the study of the tumor microenvironment have revealed significant interaction between tumor cells and their surrounding stroma in model systems. We have previously shown that two distinct stromal signatures derived from a macrophage (CSF1) response and a fibroblastic (DTF-like) response are present in subsets of invasive breast cancers and show a correlation with clinical outcome. In the present study we explore whether these signatures also exist in the stroma of ductal carcinoma in situ (DCIS). We studied the signatures by both gene expression profile analysis of a publically available data set of DCIS and by immunohistochemistry (IHC) on a tissue microarray of DCIS and invasive breast cancer cases. Both the gene expression and immunohistochemical data show that the macrophage response and fibroblast expression signatures are present in the stroma of subsets of DCIS cases. The incidence of the stromal signatures in DCIS is similar to the incidence in invasive breast cancer that we have previously reported. We also find that the macrophage response signature is associated with higher grade DCIS and cases which are ER and PR negative, whereas the fibroblast signature was not associated with any clinicopathologic features in DCIS. A comparison of 115 matched cases of DCIS and invasive breast cancer found a correlation between the type of stromal response in DCIS and invasive ductal carcinoma (IDC) within the same patient for both the macrophage response and the fibroblast stromal signatures (P = 0.03 and 0.08, respectively). This study is a first characterization of these signatures in DCIS. These signatures have significant clinicopathologic associations and tend to be conserved as the tumor progresses from DCIS to invasive breast cancer.

摘要

近年来,对肿瘤微环境的研究进展揭示了模型系统中肿瘤细胞与其周围基质之间的显著相互作用。我们之前已经表明,两种不同的基质特征,即源自巨噬细胞(CSF1)反应的特征和源自成纤维细胞(DTF 样)反应的特征,存在于浸润性乳腺癌的亚群中,并与临床结果相关。在本研究中,我们探讨了这些特征是否也存在于导管原位癌(DCIS)的基质中。我们通过公共 DCIS 数据集的基因表达谱分析和 DCIS 和浸润性乳腺癌病例的组织微阵列免疫组织化学(IHC)来研究这些特征。基因表达和免疫组织化学数据均表明,巨噬细胞反应和成纤维细胞表达特征存在于亚组 DCIS 病例的基质中。DCIS 中基质特征的发生率与我们之前报道的浸润性乳腺癌的发生率相似。我们还发现,巨噬细胞反应特征与高级别 DCIS 和 ER 和 PR 阴性病例相关,而成纤维细胞特征与 DCIS 中的任何临床病理特征均无关。对 115 对匹配的 DCIS 和浸润性乳腺癌病例的比较发现,在同一患者中,DCIS 和浸润性导管癌(IDC)中的基质反应类型与巨噬细胞反应和成纤维细胞基质特征之间存在相关性(分别为 P = 0.03 和 0.08)。本研究首次对这些特征在 DCIS 中的特征进行了描述。这些特征具有显著的临床病理相关性,并倾向于在肿瘤从 DCIS 进展为浸润性乳腺癌时保持保守。

相似文献

1
Analysis of stromal signatures in the tumor microenvironment of ductal carcinoma in situ.
Breast Cancer Res Treat. 2010 Sep;123(2):397-404. doi: 10.1007/s10549-009-0654-0. Epub 2009 Dec 1.
2
Breast carcinoma in sclerosing adenosis: a clinicopathological and immunophenotypical analysis on 206 lesions.
J Clin Pathol. 2018 Jun;71(6):546-553. doi: 10.1136/jclinpath-2017-204751. Epub 2018 Feb 7.
4
Ductal carcinoma in situ of the breast: the importance of morphologic and molecular interactions.
Hum Pathol. 2016 Mar;49:114-23. doi: 10.1016/j.humpath.2015.11.003. Epub 2015 Nov 17.
5
Gene expression profiling of tumour epithelial and stromal compartments during breast cancer progression.
Breast Cancer Res Treat. 2012 Aug;135(1):153-65. doi: 10.1007/s10549-012-2123-4. Epub 2012 Jun 21.
6
Stromal signatures in endometrioid endometrial carcinomas.
Mod Pathol. 2014 Apr;27(4):631-9. doi: 10.1038/modpathol.2013.131. Epub 2013 Nov 22.
8
Molecular diversity in ductal carcinoma in situ (DCIS) and early invasive breast cancer.
Mol Oncol. 2010 Aug;4(4):357-68. doi: 10.1016/j.molonc.2010.06.007. Epub 2010 Jun 26.
10
Differential Gene Expression in Ductal Carcinoma In Situ of the Breast Based on ERBB2 Status.
Cancer Control. 2017 Jan;24(1):102-110. doi: 10.1177/107327481702400117.

引用本文的文献

3
Tumor microenvironmental determinants of high-risk DCIS progression.
Res Sq. 2024 May 9:rs.3.rs-4126092. doi: 10.21203/rs.3.rs-4126092/v1.
6
TGFβ-mediated MMP13 secretion drives myoepithelial cell dependent breast cancer progression.
NPJ Breast Cancer. 2023 Mar 2;9(1):9. doi: 10.1038/s41523-023-00513-6.
7
Macrophage density is an adverse prognosticator for ipsilateral recurrence in ductal carcinoma in situ.
Breast. 2022 Aug;64:35-40. doi: 10.1016/j.breast.2022.04.004. Epub 2022 Apr 22.
10
Cancer-Associated Fibroblasts in Breast Cancer Treatment Response and Metastasis.
Cancers (Basel). 2021 Jun 23;13(13):3146. doi: 10.3390/cancers13133146.

本文引用的文献

2
Role of COX-2 in epithelial-stromal cell interactions and progression of ductal carcinoma in situ of the breast.
Proc Natl Acad Sci U S A. 2009 Mar 3;106(9):3372-7. doi: 10.1073/pnas.0813306106. Epub 2009 Feb 13.
3
The macrophage colony-stimulating factor 1 response signature in breast carcinoma.
Clin Cancer Res. 2009 Feb 1;15(3):778-87. doi: 10.1158/1078-0432.CCR-08-1283.
4
Comedo-ductal carcinoma in situ: A paradoxical role for programmed cell death.
Cancer Biol Ther. 2008 Nov;7(11):1774-82. doi: 10.4161/cbt.7.11.6781. Epub 2008 Nov 12.
5
The fibromatosis signature defines a robust stromal response in breast carcinoma.
Lab Invest. 2008 Jun;88(6):591-601. doi: 10.1038/labinvest.2008.31. Epub 2008 Apr 14.
7
Tumor stroma and regulation of cancer development.
Annu Rev Pathol. 2006;1:119-50. doi: 10.1146/annurev.pathol.1.110304.100224.
9
Mesenchymal stem cells within tumour stroma promote breast cancer metastasis.
Nature. 2007 Oct 4;449(7162):557-63. doi: 10.1038/nature06188.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验