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The PI3K/Akt/mTOR pathway is activated in murine lupus nephritis and downregulated by rapamycin
Author(s) -
Kostas Stylianou,
Ioannis Petrakis,
Vasiliki Mavroeidi,
Stavros Stratakis,
Eleftheria Vardaki,
Kostas Perakis,
Spyros Stratigis,
Andreas Passam,
Eva Papadogiorgaki,
K. Giannakakis,
Lydia Nakopoulou,
Eugene Daphnis
Publication year - 2010
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/gfq496
Subject(s) - pi3k/akt/mtor pathway , protein kinase b , rptor , lupus nephritis , medicine , cancer research , sirolimus , signal transduction , immunology , biology , microbiology and biotechnology , disease
The mammalian target of rapamycin (mTOR) inhibitor, rapamycin, has been shown to inhibit the progression of murine lupus nephritis by virtue of its potent immunosuppressive properties. The phosphoinositol-3-kinase (PI3K)/Akt pathway is a major upstream activator of mTOR and has been implicated in the propagation of cancer and autoimmunity. However, the activation status of the PI3K/Akt/mTOR pathway in lupus nephritis has not been studied so far.

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