Cdc42 promotes transendothelial migration of cancer cells through β1 integrin.

Cancer cells interact with endothelial cells during the process of metastatic spreading. Here, we use a small interfering RNA screen targeting Rho GTPases in cancer cells to identify Cdc42 as a critical regulator of cancer cell-endothelial cell interactions and transendothelial migration. We find th...

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Main Authors: Reymond, N, Im, J, Garg, R, Vega, F, Borda d'Agua, B, Riou, P, Cox, S, Valderrama, F, Muschel, R, Ridley, A
Format: Journal article
Language:English
Published: 2012
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author Reymond, N
Im, J
Garg, R
Vega, F
Borda d'Agua, B
Riou, P
Cox, S
Valderrama, F
Muschel, R
Ridley, A
author_facet Reymond, N
Im, J
Garg, R
Vega, F
Borda d'Agua, B
Riou, P
Cox, S
Valderrama, F
Muschel, R
Ridley, A
author_sort Reymond, N
collection OXFORD
description Cancer cells interact with endothelial cells during the process of metastatic spreading. Here, we use a small interfering RNA screen targeting Rho GTPases in cancer cells to identify Cdc42 as a critical regulator of cancer cell-endothelial cell interactions and transendothelial migration. We find that Cdc42 regulates β1 integrin expression at the transcriptional level via the transcription factor serum response factor (SRF). β1 integrin is the main target for Cdc42-mediating interaction of cancer cells with endothelial cells and the underlying extracellular matrix, as exogenous β1 integrin expression was sufficient to rescue the Cdc42-silencing phenotype. We show that Cdc42 was required in vivo for cancer cell spreading and protrusion extension along blood vessels and retention in the lungs. Interestingly, transient Cdc42 depletion was sufficient to decrease experimental lung metastases, which suggests that its role in endothelial attachment is important for metastasis. By identifying β1 integrin as a transcriptional target of Cdc42, our results provide new insight into Cdc42 function.
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spelling oxford-uuid:62e451dd-b027-4644-aff5-1329ef4ae94e2022-03-26T18:09:18ZCdc42 promotes transendothelial migration of cancer cells through β1 integrin.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:62e451dd-b027-4644-aff5-1329ef4ae94eEnglishSymplectic Elements at Oxford2012Reymond, NIm, JGarg, RVega, FBorda d'Agua, BRiou, PCox, SValderrama, FMuschel, RRidley, ACancer cells interact with endothelial cells during the process of metastatic spreading. Here, we use a small interfering RNA screen targeting Rho GTPases in cancer cells to identify Cdc42 as a critical regulator of cancer cell-endothelial cell interactions and transendothelial migration. We find that Cdc42 regulates β1 integrin expression at the transcriptional level via the transcription factor serum response factor (SRF). β1 integrin is the main target for Cdc42-mediating interaction of cancer cells with endothelial cells and the underlying extracellular matrix, as exogenous β1 integrin expression was sufficient to rescue the Cdc42-silencing phenotype. We show that Cdc42 was required in vivo for cancer cell spreading and protrusion extension along blood vessels and retention in the lungs. Interestingly, transient Cdc42 depletion was sufficient to decrease experimental lung metastases, which suggests that its role in endothelial attachment is important for metastasis. By identifying β1 integrin as a transcriptional target of Cdc42, our results provide new insight into Cdc42 function.
spellingShingle Reymond, N
Im, J
Garg, R
Vega, F
Borda d'Agua, B
Riou, P
Cox, S
Valderrama, F
Muschel, R
Ridley, A
Cdc42 promotes transendothelial migration of cancer cells through β1 integrin.
title Cdc42 promotes transendothelial migration of cancer cells through β1 integrin.
title_full Cdc42 promotes transendothelial migration of cancer cells through β1 integrin.
title_fullStr Cdc42 promotes transendothelial migration of cancer cells through β1 integrin.
title_full_unstemmed Cdc42 promotes transendothelial migration of cancer cells through β1 integrin.
title_short Cdc42 promotes transendothelial migration of cancer cells through β1 integrin.
title_sort cdc42 promotes transendothelial migration of cancer cells through β1 integrin
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