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Pericytes limit tumor cell metastasis
Xiaojie Xian, … , Holger Gerhardt, Henrik Semb
Xiaojie Xian, … , Holger Gerhardt, Henrik Semb
Published March 1, 2006
Citation Information: J Clin Invest. 2006;116(3):642-651. https://doi.org/10.1172/JCI25705.
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Research Article Oncology

Pericytes limit tumor cell metastasis

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Abstract

Previously we observed that neural cell adhesion molecule (NCAM) deficiency in β tumor cells facilitates metastasis into distant organs and local lymph nodes. Here, we show that NCAM-deficient β cell tumors grew leaky blood vessels with perturbed pericyte-endothelial cell-cell interactions and deficient perivascular deposition of ECM components. Conversely, tumor cell expression of NCAM in a fibrosarcoma model (T241) improved pericyte recruitment and increased perivascular deposition of ECM molecules. Together, these findings suggest that NCAM may limit tumor cell metastasis by stabilizing the microvessel wall. To directly address whether pericyte dysfunction increases the metastatic potential of solid tumors, we studied β cell tumorigenesis in primary pericyte-deficient Pdgfbret/ret mice. This resulted in β tumor cell metastases in distant organs and local lymph nodes, demonstrating a role for pericytes in limiting tumor cell metastasis. These data support a new model for how tumor cells trigger metastasis by perturbing pericyte-endothelial cell-cell interactions.

Authors

Xiaojie Xian, Joakim Håkansson, Anders Ståhlberg, Per Lindblom, Christer Betsholtz, Holger Gerhardt, Henrik Semb

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Figure 5

Pericyte detachment causes tumor cell dissemination in distant organs and local lymph nodes.

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Pericyte detachment causes tumor cell dissemination in distant organs an...
(A) Intercrosses of RT and Pdgfbret/ret mice result in β tumor cell dissemination in distant organs, including the liver, kidney, and intestine (arrows), and local lymph nodes (arrowheads). (B and C) Immunostainings of sections of RT adenomas and carcinomas and RTPdgfbret/ret local lymph node and distant organ metastases with Pdx1 (B) and E-cadherin (C) antibodies. Exocrine and tumor tissues are indicated by “E” and “T,” respectively. (D–G) Pancreatic tumor sections from RTNC/KO (D and F) and RTPdgfbret/ret (E and G) mice were stained with H&E. Tissue disaggregation and presence of isolated tumor cell clusters inside hemorrhagic lacunae were observed in both genotypes. Isolated cell clusters are indicated by arrows. Scale bars: 1 cm (A), 100 μm (B–E), and 50 μm (F and G).

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