Renal cell carcinoma

E Jonasch, J Gao, WK Rathmell - Bmj, 2014 - bmj.com
The treatment of renal cell carcinoma (RCC) has changed greatly over the past 15 years.
Progress in the surgical management of the primary tumor and increased understanding of …

TFEB and TFE3: linking lysosomes to cellular adaptation to stress

N Raben, R Puertollano - Annual review of cell and …, 2016 - annualreviews.org
In recent years, our vision of lysosomes has drastically changed. Formerly considered to be
mere degradative compartments, they are now recognized as key players in many cellular …

The nutrient-responsive transcription factor TFE3 promotes autophagy, lysosomal biogenesis, and clearance of cellular debris

JA Martina, HI Diab, L Lishu, L Jeong-A, S Patange… - Science …, 2014 - science.org
The discovery of a gene network regulating lysosomal biogenesis and its transcriptional
regulator transcription factor EB (TFEB) revealed that cells monitor lysosomal function and …

The genetic basis of kidney cancer: a metabolic disease

WM Linehan, R Srinivasan, LS Schmidt - Nature reviews urology, 2010 - nature.com
Kidney cancer is not a single disease but comprises a number of different types of cancer
that occur in the kidney, each caused by a different gene with a different histology and …

Birt-Hogg-Dubé syndrome: diagnosis and management

FH Menko, MAM Van Steensel, S Giraud… - The lancet …, 2009 - thelancet.com
Summary Birt-Hogg-Dubé syndrome (BHD) is an autosomal dominant condition
characterised clinically by skin fibrofolliculomas, pulmonary cysts, spontaneous …

Molecular genetics and clinical features of Birt–Hogg–Dubé syndrome

LS Schmidt, WM Linehan - Nature Reviews Urology, 2015 - nature.com
Abstract Birt–Hogg–Dubé (BHD) syndrome is an inherited renal cancer syndrome in which
affected individuals are at risk of developing benign cutaneous fibrofolliculomas, bilateral …

BHD mutations, clinical and molecular genetic investigations of Birt–Hogg–Dubé syndrome: a new series of 50 families and a review of published reports

JR Toro, MH Wei, GM Glenn, M Weinreich… - Journal of medical …, 2008 - jmg.bmj.com
Background: Birt–Hogg–Dubé syndrome (BHDS)(MIM 135150) is an autosomal dominant
predisposition to the development of follicular hamartomas (fibrofolliculomas), lung cysts …

Folliculin encoded by the BHD gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling

M Baba, SB Hong, N Sharma… - Proceedings of the …, 2006 - National Acad Sciences
Birt–Hogg–Dubé syndrome, a hamartoma disorder characterized by benign tumors of the
hair follicle, lung cysts, and renal neoplasia, is caused by germ-line mutations in the BHD …

Familial kidney cancer: implications of new syndromes and molecular insights

MI Carlo, AA Hakimi, GD Stewart, G Bratslavsky… - European urology, 2019 - Elsevier
Context Hereditary cases account for about 5% of all cases of renal cell carcinoma (RCC).
With advances in next-generation sequencing, several new hereditary syndromes have …

[HTML][HTML] Systemic treatment of renal cell cancer: A comprehensive review

A Sánchez-Gastaldo, E Kempf, AG Del Alba… - Cancer treatment …, 2017 - Elsevier
Kidney cancer represents about 5% of all new cancer diagnoses. The most common form of
kidney cancer arises from renal epithelium, named renal cell carcinoma (RCC). This entity …