Targeting the PI3K/Akt/mTOR pathway: effective combinations and clinical considerations

J LoPiccolo, GM Blumenthal, WB Bernstein… - Drug Resistance …, 2008 - Elsevier
The PI3K/Akt/mTOR pathway is a prototypic survival pathway that is constitutively activated
in many types of cancer. Mechanisms for pathway activation include loss of tumor …

Activation of the PI3K/Akt pathway and chemotherapeutic resistance

KA West, SS Castillo, PA Dennis - Drug resistance updates, 2002 - Elsevier
The resistance of many types of cancer to conventional chemotherapies is a major factor
undermining successful cancer treatment. In this review, the role of a signal transduction …

What turns CREB on?

M Johannessen, MP Delghandi, U Moens - Cellular signalling, 2004 - Elsevier
The transactivation domain of the cAMP response element-binding protein (CREB) consists
of two major domains. The glutamine-rich Q2 domain, which interacts with the general …

PI3K/Akt and CREB regulate adult neural hippocampal progenitor proliferation and differentiation

J Peltier, A O'Neill, DV Schaffer - Developmental neurobiology, 2007 - Wiley Online Library
The phosphoinositide 3‐OH kinase (PI3K)/Akt pathway has been implicated in regulating
several important cellular processes, including apoptosis, survival, proliferation, and …

Ion channels and signaling in the pituitary gland

SS Stojilkovic, J Tabak, R Bertram - Endocrine reviews, 2010 - academic.oup.com
Endocrine pituitary cells are neuronlike; they express numerous voltage-gated sodium,
calcium, potassium, and chloride channels and fire action potentials spontaneously …

Loss of the repressor REST in uterine fibroids promotes aberrant G protein-coupled receptor 10 expression and activates mammalian target of rapamycin pathway

BV Varghese, F Koohestani… - Proceedings of the …, 2013 - National Acad Sciences
Uterine fibroids (leiomyomas) are the most common tumors of the female reproductive tract,
occurring in up to 77% of reproductive-aged women, yet molecular pathogenesis remains …

Distinct pools of cAMP centre on different isoforms of adenylyl cyclase in pituitary-derived GH3B6 cells

S Wachten, N Masada, LJ Ayling… - Journal of cell …, 2010 - journals.biologists.com
Microdomains have been proposed to explain specificity in the myriad of possible cellular
targets of cAMP. Local differences in cAMP levels can be generated by phosphodiesterases …

RF-amide neuropeptides and their receptors in Mammals: Pharmacological properties, drug development and main physiological functions

R Quillet, S Ayachi, F Bihel, K Elhabazi, B Ilien… - Pharmacology & …, 2016 - Elsevier
RF-amide neuropeptides, with their typical Arg-Phe-NH 2 signature at their carboxyl C-
termini, belong to a lineage of peptides that spans almost the entire life tree. Throughout …

Prolactin-releasing peptide: physiological and pharmacological properties

V Pražienková, A Popelová, J Kuneš… - International Journal of …, 2019 - mdpi.com
Prolactin-releasing peptide (PrRP) belongs to the large RF-amide neuropeptide family with
a conserved Arg-Phe-amide motif at the C-terminus. PrRP plays a main role in the regulation …

Exogenous fibroblast growth factor 1 ameliorates diabetes-induced cognitive decline via coordinately regulating PI3K/AKT signaling and PERK signaling

Y Wu, C Wu, L Ye, B Wang, Y Yuan, Y Liu… - Cell Communication and …, 2020 - Springer
Background Diabetes induces central nervous system damage, leading to cognitive decline.
Fibroblast growth factor 1 (FGF1) has dual function of neuroprotection and normalizing …