]>PPAR<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mi mathvariant="bold">α</mml:mi></mml:math> Ligands as Antitumorigenic and Antiangiogenic Agents : Table 2
Table 2: PPARα and tumorigenesis: lessons from the PPARα-null mice.

Ligand Host Challenge Effect Target Reference

WY14643PPARα-null miceResistant to the development of spontaneous hepatocarcinomaInability to downregulate the miRNA let-7C[52]

WY14643 FenofibratePPARα-humanized transgenic mouseResistant to the development of spontaneous hepatocarcinomaInability to downregulate the microRNA let-7C[53, 54]

WY14643PPARα-null miceInjection of isogenic tumor cellsResistant to the Wyeth-mediated antiangiogenic and antitumorigenic activitiesInability to downregulate arachidonate epoxygenase expression[38]

DEHPPPARα-null miceDevelopment of hepatocarcinomaIncreased PPARα-independent oxidative stress[55]

WY14643 FenofibratePPARα-null miceCarotid arterial injuryIntimal hyperplasiaInability to induce the expression of the tumor suppressor p16INK4a[56]

PPARα-null miceInjection of isogenic tumor cellsResistant to the development of primary and metastatic tumor growthIncreased recruitment of granulocyte responsible for thrombospondin production[57]

PPARα-null miceIncreased susceptibility to spontaneous adenomas and hepatocellular carcinomasNot explored[58]