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Live tumor imaging shows macrophage induction and TMEM-mediated enrichment of cancer stem cells during metastatic dissemination.
Sharma, Ved P; Tang, Binwu; Wang, Yarong; Duran, Camille L; Karagiannis, George S; Xue, Emily A; Entenberg, David; Borriello, Lucia; Coste, Anouchka; Eddy, Robert J; Kim, Gina; Ye, Xianjun; Jones, Joan G; Grunblatt, Eli; Agi, Nathan; Roy, Sweta; Bandyopadhyaya, Gargi; Adler, Esther; Surve, Chinmay R; Esposito, Dominic; Goswami, Sumanta; Segall, Jeffrey E; Guo, Wenjun; Condeelis, John S; Wakefield, Lalage M; Oktay, Maja H.
Affiliation
  • Sharma VP; Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Tang B; Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Wang Y; Laboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, MD, USA.
  • Duran CL; Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Karagiannis GS; Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Xue EA; Integrated Imaging Program, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Entenberg D; Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Borriello L; Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Coste A; Integrated Imaging Program, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Eddy RJ; Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Kim G; Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Ye X; Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Jones JG; Integrated Imaging Program, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Grunblatt E; Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Agi N; Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Roy S; Department of Surgery, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Bandyopadhyaya G; Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Adler E; Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Surve CR; Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Esposito D; Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Goswami S; Integrated Imaging Program, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Segall JE; Department of Pathology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Guo W; Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Condeelis JS; Department of Biology, Yeshiva University, New York, NY, USA.
  • Wakefield LM; Department of Biology, Yeshiva University, New York, NY, USA.
  • Oktay MH; Department of Biology, Yeshiva University, New York, NY, USA.
Nat Commun ; 12(1): 7300, 2021 12 15.
Article in En | MEDLINE | ID: mdl-34911937
ABSTRACT
Cancer stem cells (CSCs) play an important role during metastasis, but the dynamic behavior and induction mechanisms of CSCs are not well understood. Here, we employ high-resolution intravital microscopy using a CSC biosensor to directly observe CSCs in live mice with mammary tumors. CSCs display the slow-migratory, invadopod-rich phenotype that is the hallmark of disseminating tumor cells. CSCs are enriched near macrophages, particularly near macrophage-containing intravasation sites called Tumor Microenvironment of Metastasis (TMEM) doorways. Substantial enrichment of CSCs occurs on association with TMEM doorways, contributing to the finding that CSCs represent >60% of circulating tumor cells. Mechanistically, stemness is induced in non-stem cancer cells upon their direct contact with macrophages via Notch-Jagged signaling. In breast cancers from patients, the density of TMEM doorways correlates with the proportion of cancer cells expressing stem cell markers, indicating that in human breast cancer TMEM doorways are not only cancer cell intravasation portals but also CSC programming sites.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Neoplastic Stem Cells / Breast Neoplasms / Macrophages Limits: Animals / Female / Humans Language: En Year: 2021 Type: Article

Full text: 1 Database: MEDLINE Main subject: Neoplastic Stem Cells / Breast Neoplasms / Macrophages Limits: Animals / Female / Humans Language: En Year: 2021 Type: Article