Please use this identifier to cite or link to this item:
https://hdl.handle.net/10356/173163
Title: | Adipose-enriched peri-tumoral stroma, in contrast to myofibroblast-enriched stroma, prognosticates poorer survival in breast cancers | Authors: | Lau, Hannah Si Hui Tan, Veronique Kiak Mien Tan, Benita Kiat Tee Sim, Yirong Quist, Jelmar Thike, Aye Aye Tan, Puay Hoon Pervaiz, Shazib Grigoriadis, Anita Sabapathy, Kanaga |
Keywords: | Science::Medicine Science::Biological sciences |
Issue Date: | 2023 | Source: | Lau, H. S. H., Tan, V. K. M., Tan, B. K. T., Sim, Y., Quist, J., Thike, A. A., Tan, P. H., Pervaiz, S., Grigoriadis, A. & Sabapathy, K. (2023). Adipose-enriched peri-tumoral stroma, in contrast to myofibroblast-enriched stroma, prognosticates poorer survival in breast cancers. NPJ Breast Cancer, 9(1), 84-. https://dx.doi.org/10.1038/s41523-023-00590-7 | Project: | NCCSPG-YR2015-JAN-7 | Journal: | NPJ Breast Cancer | Abstract: | Despite our understanding of the genetic basis of intra-tumoral heterogeneity, the role of stromal heterogeneity arising from an altered tumor microenvironment in affecting tumorigenesis is poorly understood. In particular, extensive study on the peri-tumoral stroma in the morphologically normal tissues surrounding the tumor is lacking. Here, we examine the heterogeneity in tumors and peri-tumoral stroma from 8 ER+/PR+/HER2- invasive breast carcinomas, through multi-region transcriptomic profiling by microarray. We describe the regional heterogeneity observed at the intrinsic molecular subtype, pathway enrichment, and cell type composition levels within each tumor and its peri-tumoral region, up to 7 cm from the tumor margins. Moreover, we identify a pro-inflammatory adipose-enriched peri-tumoral subtype which was significantly associated with poorer overall survival in breast cancer patients, in contrast to an adaptive immune cell- and myofibroblast-enriched subtype. These data together suggest that peri-tumoral heterogeneity may be an important determinant of the evolution and treatment of breast cancers. | URI: | https://hdl.handle.net/10356/173163 | ISSN: | 2374-4677 | DOI: | 10.1038/s41523-023-00590-7 | Schools: | School of Biological Sciences | Organisations: | National Cancer Centre | Rights: | © The Author(s) 2023. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http:// creativecommons.org/licenses/by/4.0/. | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
Appears in Collections: | SBS Journal Articles |
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s41523-023-00590-7.pdf | 7.38 MB | Adobe PDF | ![]() View/Open |
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