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. 2021 Mar 22;5:26. doi: 10.1038/s41698-021-00160-9

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© The Author(s) 2021

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/.

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Fig. 6 — Adipose stromal cells (ASC) derived from WAT are the principal source of CXCL12 driving cancer by increasing the survival and proliferation of cancer cells and subsequently their EMT and aggressiveness via CXCR4-mediated signaling. Lightning bolt: D-CAN as a proof-of-principal experimental therapeutic that can be used to deplete ASC and suppress cancer progression.