[HTML][HTML] The roles of MAPKs in disease

MC Lawrence, A Jivan, C Shao, L Duan, D Goad… - Cell research, 2008 - nature.com
MAP kinases transduce signals that are involved in a multitude of cellular pathways and
functions in response to a variety of ligands and cell stimuli. Aberrant or inappropriate …

[HTML][HTML] A TR (i) P to cell migration: New roles of TRP channels in mechanotransduction and cancer

J Canales, D Morales, C Blanco, J Rivas… - Frontiers in …, 2019 - frontiersin.org
Cell migration is a key process in cancer metastasis, allowing malignant cells to spread from
the primary tumor to distant organs. At the molecular level, migration is the result of several …

Cyst formation and activation of the extracellular regulated kinase pathway after kidney specific inactivation of Pkd1

S Shibazaki, Z Yu, S Nishio, X Tian… - Human molecular …, 2008 - academic.oup.com
Polycystic kidney disease (ADPKD) results from failure of the kidney to properly maintain
three-dimensional structure after loss of either polycystin-1 or-2. Mice with kidney selective …

Polycystin-1 C-terminal tail associates with β-catenin and inhibits canonical Wnt signaling

M Lal, X Song, JL Pluznick, V Di Giovanni… - Human molecular …, 2008 - academic.oup.com
Abstract Polycystin-1 (PC1), the product of the PKD1 gene mutated in the majority of
autosomal dominant polycystic kidney disease (ADPKD) cases, undergoes a cleavage …

The ADPKD genes pkd1a/b and pkd2 regulate extracellular matrix formation

S Mangos, P Lam, A Zhao, Y Liu… - Disease models & …, 2010 - journals.biologists.com
SUMMARY Mutations in polycystin1 (PKD1) account for the majority of autosomal dominant
polycystic kidney disease (ADPKD). PKD1 mutations are also associated with vascular …

Polycystin-2 and phosphodiesterase 4C are components of a ciliary A-kinase anchoring protein complex that is disrupted in cystic kidney diseases

YH Choi, A Suzuki, S Hajarnis, Z Ma… - Proceedings of the …, 2011 - National Acad Sciences
Polycystic kidney disease (PKD) is a genetic disorder that is characterized by cyst formation
in kidney tubules. PKD arises from abnormalities of the primary cilium, a sensory organelle …

Extracellular matrix, integrins, and focal adhesion signaling in polycystic kidney disease

Y Zhang, G Reif, DP Wallace - Cellular signalling, 2020 - Elsevier
In autosomal dominant polycystic kidney disease (ADPKD), the inexorable growth of
numerous fluid-filled cysts leads to massively enlarged kidneys, renal interstitial damage …

TRPM8 inhibits endothelial cell migration via a non-channel function by trapping the small GTPase Rap1

T Genova, GP Grolez, C Camillo, M Bernardini… - Journal of Cell …, 2017 - rupress.org
Endothelial cell adhesion and migration are critical steps of the angiogenic process, whose
dysfunction is associated with tumor growth and metastasis. The TRPM8 channel has …

Calcium signaling in polycystic kidney disease-cell death and survival

KM Márquez-Nogueras, V Vuchkovska, IY Kuo - Cell Calcium, 2023 - Elsevier
Polycystic kidney disease is typified by cysts in the kidney and extra-renal manifestations
including hypertension and heart failure. The main genetic underpinning this disease are …

[HTML][HTML] Emerging evidence of a link between the polycystins and the mTOR pathways

A Boletta - Pathogenetics, 2009 - Springer
Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disease characterized
by the formation of renal cysts. This disease can be caused by mutations in two genes …