Platelet derived growth factor increases phospholipase D1 but not phospholipase D2 expression via NFkappaB signaling pathway and enhances invasion of breast cancer cells.

Cancer Lett

Department of Molecular Biology, College of Natural Science, Pusan National University, 30 Jangjeon dong, Busan, Republic of Korea.

Published: August 2010

AI Article Synopsis

  • Phospholipase D (PLD) plays a key role in cell growth signaling, particularly in its regulation during cancer development.
  • Platelet-derived growth factor (PDGF) specifically increases the expression of PLD1, not PLD2, through the Ras-ERK/PI3K-NFkappaB signaling pathway in SK-BR3 breast cancer cells.
  • Reducing PLD1 levels significantly inhibits PDGF-driven increases in matrix metalloproteinases and the invasiveness of breast cancer cells, suggesting that PDGF-induced PLD1 expression may promote cancer progression.

Article Abstract

Phospholipase D (PLD) has emerged as a critical element in the cell growth signaling. Despite extensive information regarding the regulation of PLD activity in cell survival, the signaling mechanisms that regulate PLD expression in cancer remains poorly understood. Here we investigate that platelet derived growth factor (PDGF) increases PLD1 but not PLD2 expression via Ras-ERK/PI3K-NFkappaB signaling cascade in SK-BR3 breast cancer cells. The two NFkappaB-binding sites are functionally critical for transcriptional activation of PLD1 induced by PDGF. Furthermore, depletion of PLD1 using siRNA significantly abolished PDGF-induced upregulation of matrix metalloproteinase-2 or -9 and invasion of breast cancer cells. Thus, we propose that PDGF-induced PLD1 expression via NFkappaB signaling pathway might contribute to carcinogenesis.

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Source
http://dx.doi.org/10.1016/j.canlet.2010.01.031DOI Listing

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