Transition to invasive breast cancer is associated with progressive changes in the structure and composition of tumor stroma

Author:

Risom TylerORCID,Glass David R,Liu Candace C,Rivero-Gutiérrez Belén,Baranski Alex,McCaffrey Erin FORCID,Greenwald Noah F,Kagel Adam,Strand Siri H,Varma Sushama,Kong Alex,Keren Leeat,Srivastava Sucheta,Zhu Chunfang,Khair Zumana,Veis Deborah J,Deschryver Katherine,Vennam Sujay,Maley Carlo,Hwang E Shelley,Marks Jefferey R,Bendall Sean CORCID,Colditz Graham A,West Robert B,Angelo MichaelORCID

Abstract

AbstractDuctal carcinomain situ(DCIS) is a pre-invasive lesion that is thought to be a precursor to invasive breast cancer (IBC). To understand how the tumor microenvironment (TME) changes with transition to IBC, we used Multiplexed Ion Beam Imaging by time of flight (MIBI-TOF) and a 37-plex antibody staining panel to analyze 140 clinically annotated surgical resections covering the full spectrum of breast cancer progression. We compared normal, DCIS, and IBC tissues using machine learning tools for multiplexed cell segmentation, pixel-based clustering, and object morphometrics. Transition from DCIS to IBC was found to occur along a trajectory marked by coordinated shifts in location and function of myoepithelium, fibroblasts, and infiltrating immune cells in the surrounding stroma. Taken together, this comprehensive study within the HTAN Breast PreCancer Atlas offers insight into the etiologies of DCIS, its transition to IBC, and emphasizes the importance of the TME stroma in promoting these processes.

Publisher

Cold Spring Harbor Laboratory

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