Needle biopsy accelerates pro-metastatic changes and systemic dissemination in breast cancer: Implications for mortality by surgery delay

  • Cell Rep Med. 2023 Dec 19;4(12):101330. doi: 10.1016/j.xcrm.2023.101330.
Hiroyasu Kameyama  1 Priya Dondapati  1 Reese Simmons  1 Macall Leslie  1 John F Langenheim  2 Yunguang Sun  3 Misung Yi  4 Aubrey Rottschaefer  1 Rashmi Pathak  1 Shreya Nuguri  1 Kar-Ming Fung  5 Shirng-Wern Tsaih  6 Inna Chervoneva  4 Hallgeir Rui  2 Takemi Tanaka  7
Affiliations
  • 1. Stephenson Cancer Center, University of Oklahoma Health Sciences Center, 975 NE 10th St., Oklahoma City, OK 73104, USA.
  • 2. Department of Pharmacology, Physiology & Cancer Biology, Sidney Kimmel Cancer Center, Thomas Jefferson University, 233 S 10th St., BLSB 1008, Philadelphia, PA 19107, USA.
  • 3. Department of Pathology, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USA.
  • 4. Division of Biostatistics, Department of Pharmacology, Physiology & Cancer Biology, Sidney Kimmel Cancer Center, Thomas Jefferson University, 233 S 10th St., BLSB 1008, Philadelphia, PA 19107, USA.
  • 5. Department of Pathology, School of Medicine, University of Oklahoma Health Sciences Center, 940 Stanton L Young Boulevard, Oklahoma City, OK 73104, USA.
  • 6. Department of Obstetrics and Gynecology, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USA.
  • 7. Stephenson Cancer Center, University of Oklahoma Health Sciences Center, 975 NE 10th St., Oklahoma City, OK 73104, USA; Department of Pathology, School of Medicine, University of Oklahoma Health Sciences Center, 940 Stanton L Young Boulevard, Oklahoma City, OK 73104, USA. Electronic address: [email protected].
Abstract

Increased Breast Cancer (BC) mortality risk posed by delayed surgical resection of tumor after diagnosis is a growing concern, yet the underlying mechanisms remain unknown. Our cohort analyses of early-stage BC patients reveal the emergence of a significantly rising mortality risk when the biopsy-to-surgery interval was extended beyond 53 days. Additionally, histology of post-biopsy Tumors shows prolonged retention of a metastasis-permissive wound stroma dominated by M2-like Macrophages capable of promoting Cancer cell epithelial-to-mesenchymal transition and angiogenesis. We show that needle biopsy promotes systemic dissemination of Cancer cells through a mechanism of sustained activation of the COX-2/PGE2/EP2 feedforward loop, which favors M2 polarization and its associated pro-metastatic changes but are abrogated by oral treatment with COX-2 or EP2 inhibitors in estrogen-receptor-positive (ER+) syngeneic mouse tumor models. Therefore, we conclude that needle biopsy of ER+ BC provokes progressive pro-metastatic changes, which may explain the mortality risk posed by surgery delay after diagnosis.

Keywords
COX-2; EP2; M2 macrophage; breast cancer; epithelial-mesenchymal transition; metastasis; needle biopsy; prostaglandin E(2); surgery delay; wound healing.
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