Results 41 to 50 of about 3,802 (167)

TMEM16A inhibits angiotensin II-induced basilar artery smooth muscle cell migration in a WNK1-dependent manner

open access: yesActa Pharmaceutica Sinica B, 2021
Vascular smooth muscle cell (VSMC) migration plays a critical role in the pathogenesis of many cardiovascular diseases. We recently showed that TMEM16A is involved in hypertension-induced cerebrovascular remodeling.
Huaqing Zheng   +10 more
doaj   +1 more source

Identification of the Novel TMEM16A Inhibitor Dehydroandrographolide and Its Anticancer Activity on SW620 Cells.

open access: yesPLoS ONE, 2015
TMEM16A, a calcium-activated chloride channel (CaCC), is highly amplified and expressed in human cancers and is involved in the growth and metastasis of some malignancies. Inhibition of TMEM16A represents a novel pharmaceutical approach for the treatment
Yujie Sui   +11 more
doaj   +1 more source

Expression of TMEM16A and SLC4A4 in Human Pancreatic Islets [PDF]

open access: yesCellular Physiology and Biochemistry, 2012
Stimulation of insulin release by D-glucose is accompanied by Cl(-) and HCO(3)(-) efflux from pancreatic islet cells. The efflux of these anions may involve volume-regulated anion channels, including possibly TMEM16A, and the Na(+)-HCO(3)(-)-cotransporter SLC4A4.
Hanzu, Felicia A   +7 more
openaire   +3 more sources

TMEM16A Plays an Insignificant Role in Myocardium Remodeling but May Promote Angiogenesis of Heart During Pressure-overload

open access: yesFrontiers in Physiology, 2022
Background: Cardiac hypertrophy (CH) occurs with an increase in myocardium mass as an adaptive compensation to increased stress. Prolonged CH causes decompensated heart failure (HF).
Yaofang Zhang   +4 more
doaj   +1 more source

TMEM16A chloride channel does not drive mucus production

open access: yesLife Science Alliance, 2019
Despite being essential for airway hydration, TMEM16A is not required for mucus (MUC5AC) production. Cell proliferation is the main driver for TMEM16A up-regulation during inflammation.
Filipa B Simões   +7 more
doaj   +1 more source

Cell-specific mechanisms of TMEM16A Ca2+-activated chloride channel in cancer

open access: yesMolecular Cancer, 2017
TMEM16A (known as anoctamin 1) Ca2+-activated chloride channel is overexpressed in many tumors. TMEM16A overexpression can be caused by gene amplification in many tumors harboring 11q13 amplification.
Hui Wang   +6 more
doaj   +1 more source

Epithelial Chloride Transport by CFTR Requires TMEM16A [PDF]

open access: yesScientific Reports, 2017
AbstractCystic Fibrosis Transmembrane Conductance Regulator (CFTR) is the secretory chloride/bicarbonate channel in airways and intestine that is activated through ATP binding and phosphorylation by protein kinase A, but fails to operate in cystic fibrosis (CF).
Roberta Benedetto   +8 more
openaire   +3 more sources

ANO1 (TMEM16A) in pancreatic ductal adenocarcinoma (PDAC) [PDF]

open access: yesPflügers Archiv - European Journal of Physiology, 2014
Pancreatic ductal adenocarcinoma (PDAC) has one of the worst survival rates of all cancers. ANO1 (TMEM16A) is a recently identified Ca(2+)-activated Cl(-) channel (CaCC) that is upregulated in several tumors. Although ANO1 was subject to extensive studies in the recent years, its pathophysiological function has only been poorly understood.
Sauter, Daniel Rafael Peter   +4 more
openaire   +4 more sources

TMEM16A as a potential treatment target for head and neck cancer

open access: yesJournal of Experimental & Clinical Cancer Research, 2022
Transmembrane protein 16A (TMEM16A) forms a plasma membrane-localized Ca2+-activated Cl- channel. Its gene has been mapped to an area on chromosome 11q13, which is amplified in head and neck squamous cell carcinoma (HNSCC).
Kohei Okuyama, Souichi Yanamoto
doaj   +1 more source

Inhibition of TMEM16A by Natural Product Silibinin: Potential Lead Compounds for Treatment of Lung Adenocarcinoma

open access: yesFrontiers in Pharmacology, 2021
Background: Effective anticancer therapy can be achieved by identifying novel tumor-specific drug targets and screening of new drugs. Recently, TMEM16A has been identified to be overexpressed in lung adenocarcinoma, and inhibitors of TMEM16A showed ...
Shuai Guo   +9 more
doaj   +1 more source

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