Ral signaling pathway in health and cancer

Adel Rezaei Moghadam(University of Manitoba), Elham Patrad(University of Kansas), Elham Tafsiri(NewYork–Presbyterian Hospital), Warner Peng(University of Kansas), Benjamin David Fangman(University of Kansas), Timothy Pluard(Saint Luke's Hospital), Anthony Accurso(University of Kansas), Michael Salacz(University of Kansas), Kushal Shah(University of Kansas), Brandon Ricke(University of Kansas), Danse Bi(University of Kansas), Kyle S. Kimura(University of Kansas), Leland Graves(University of Kansas), Marzieh Khajoie Najad(University of Kansas), Roya Dolatkhah(University of Kansas), Zohreh Sanaat(University of Kansas), Mina Yazdi(University of Kansas), Naeimeh Tavakolinia(University of Kansas), Mohammad Mazani(Pasteur Institute of Iran), Mojtaba Amani(Pasteur Institute of Iran), Saeid Ghavami(University of Manitoba), Robyn Gartell(NewYork–Presbyterian Hospital), Colleen Reilly(University of Kansas), Zaid Naima(University of Kansas), Tuba Esfandyari(University of Kansas), Faris Farassati(Research Medical Center)
Cancer Medicine
October 18, 2017
Cited by 60Open Access
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Abstract

The Ral (Ras-Like) signaling pathway plays an important role in the biology of cells. A plethora of effects is regulated by this signaling pathway and its prooncogenic effectors. Our team has demonstrated the overactivation of the RalA signaling pathway in a number of human malignancies including cancers of the liver, ovary, lung, brain, and malignant peripheral nerve sheath tumors. Additionally, we have shown that the activation of RalA in cancer stem cells is higher in comparison with differentiated cancer cells. In this article, we review the role of Ral signaling in health and disease with a focus on the role of this multifunctional protein in the generation of therapies for cancer. An improved understanding of this pathway can lead to development of a novel class of anticancer therapies that functions on the basis of intervention with RalA or its downstream effectors.


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