A synthetic metastatic niche reveals antitumor neutrophils drive breast cancer metastatic dormancy in the lungs.
Jing WangRamon Ocadiz-RuizMatthew S HallGrace G BushnellSophia M OrbachJoseph T DeckerRavi M RaghaniYining ZhangAaron H MorrisJacqueline S JerussLonnie D SheaPublished in: Nature communications (2023)
Biomaterial scaffolds mimicking the environment in metastatic organs can deconstruct complex signals and facilitate the study of cancer progression and metastasis. Here we report that a subcutaneous scaffold implant in mouse models of metastatic breast cancer in female mice recruits lung-tropic circulating tumor cells yet suppresses their growth through potent in situ antitumor immunity. In contrast, the lung, the endogenous metastatic organ for these models, develops lethal metastases in aggressive breast cancer, with less aggressive tumor models developing dormant lungs suppressing tumor growth. Our study reveals multifaceted roles of neutrophils in regulating metastasis. Breast cancer-educated neutrophils infiltrate the scaffold implants and lungs, secreting the same signal to attract lung-tropic circulating tumor cells. Second, antitumor and pro-tumor neutrophils are selectively recruited to the dormant scaffolds and lungs, respectively, responding to distinct groups of chemoattractants to establish activated or suppressive immune environments that direct different fates of cancer cells.
Keyphrases
- circulating tumor cells
- squamous cell carcinoma
- small cell lung cancer
- tissue engineering
- metastatic breast cancer
- signaling pathway
- mouse model
- circulating tumor
- magnetic resonance
- magnetic resonance imaging
- soft tissue
- computed tomography
- young adults
- lymph node metastasis
- anti inflammatory
- skeletal muscle
- childhood cancer
- metabolic syndrome
- wild type