Increased ROS production in non-polarized mammary epithelial cells induces monocyte infiltration in 3D culture

Linzhang Li, Jie Chen, Gaofeng Xiong, Daret K. St Clair, Wei Xu, Ren Xu

Research output: Contribution to journalArticlepeer-review

20 Scopus citations


Loss of epithelial cell polarity promotes cell invasion and cancer dissemination. Therefore, identification of factors that disrupt polarized acinar formation is crucial. Reactive oxygen species (ROS) drive cancer progression and promote inflammation. Here, we show that the non-polarized breast cancer cell line T4-2 generates significantly higher ROS levels than polarized S1 and T4R cells in three-dimensional (3D) culture, accompanied by induction of the nuclear factor κB (NF-κB) pathway and cytokine expression. Minimizing ROS in T4-2 cells with antioxidants reestablished basal polarity and inhibited cell proliferation. Introducing constitutively activated RAC1 disrupted cell polarity and increased ROS levels, indicating that RAC1 is a crucial regulator that links cell polarity and ROS generation. We also linked monocyte infiltration with disruption of polarized acinar structure using a 3D co-culture system. Gain- and loss-of-function experiments demonstrated that increased ROS in non-polarized cells is necessary and sufficient to enhance monocyte recruitment. ROS also induced cytokine expression and NF-κB activity. These results suggest that increased ROS production in mammary epithelial cell leads to disruption of cell polarity and promotes monocyte infiltration.

Original languageEnglish
Pages (from-to)190-202
Number of pages13
JournalJournal of Cell Science
Issue number1
StatePublished - 2017

Bibliographical note

Publisher Copyright:
© 2017. Published by The Company of Biologists Ltd.


  • 3D cell culture
  • Breast cancer
  • Inflammation
  • Monocyte infiltration
  • Reactive oxygen species
  • Tissue polarity

ASJC Scopus subject areas

  • Cell Biology


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