Terfenadine, a histamine H1 receptor antagonist, induces apoptosis by suppressing STAT3 signaling in human colorectal cancer HCT116 cells [PDF]
IntroductionColorectal cancer is a highly aggressive and metastatic cancer with inadequate clinical outcomes. Given the crucial role of histamine and histamine receptors in colorectal carcinogenesis, this study aimed at exploring the anticancer effects ...
Manoj Kumar Baniya +2 more
doaj +4 more sources
Inhibitory effect of terfenadine on Kir2.1 and Kir2.3 channels [PDF]
Terfenadine is a second-generation H1-antihistamine that despite potentially can produce severe side effects it has recently gained attention due to its anticancer properties. Lately, the subfamily 2 of inward rectifier potassium channels (Kir2) has been
Delgado-Ramírez Mayra +5 more
doaj +3 more sources
Antihistamine drug terfenadine suppressed the cycle progression of gastric cancer cells by targeting PI3K/AKT/mTOR signaling [PDF]
BackgroundGastric cancer (GC) remains a leading cause of cancer-related mortality worldwide, highlighting the urgent need for effective and accessible therapies. Drug repurposing offers a cost-effective strategy to identify novel candidates from approved
Yanping Zhu +11 more
doaj +2 more sources
Repurposing terfenadine and domperidone for inhibition of apoptotic gene association in colorectal cancer: A system pharmacology approach integrated with molecular docking, MD simulations, and post-MD simulation analysis [PDF]
Colorectal cancer (CRC) remains a leading cause of global cancer mortality, underscoring the need for novel therapeutic strategies. This study used a systems pharmacology approach integrated with molecular docking and molecular dynamics (MD) simulations ...
Pushpaveni C +7 more
doaj +2 more sources
Repurposing Terfenadine as a Novel Antigiardial Compound
Giardia lamblia is a highly infectious protozoan that causes giardiasis, a gastrointestinal disease with short-term and long-lasting symptoms. The currently available drugs for giardiasis treatment have limitations such as side effects and drug ...
Daniel Osmar Suárez-Rico +6 more
doaj +2 more sources
In vivo visualization of cardiac extracellular adenosine dynamics and its pharmacological modulation in zebrafish heart failure models [PDF]
Heart failure (HF) remains a major clinical challenge with poor prognosis despite extensive research and established treatments. Extracellular ATP and adenosine (Ado), as damage-associated molecular patterns (DAMPs), contribute to HF pathogenesis through
Phurpa Phurpa +12 more
doaj +2 more sources
Proteomic and functional profiling of suspended jejunal enteroids reveals pharmacokinetic fidelity to native intestine [PDF]
Summary: Intestinal enteroids are “mini-guts” that recapitulate essential features of the intestinal epithelium in vitro . We developed and characterized native basal-out (BO) and morphogenically everted apical-out (AO) jejunal enteroids cultured in ...
Foteini Tzioufa +17 more
doaj +2 more sources
In silico exploration of anti-prostate cancer compounds from differential expressed genes [PDF]
Prostate cancer (PCa) is a complex and biologically diverse disease with no curative treatment options at present. This study aims to utilize computational methods to explore potential anti-PCa compounds based on differentially expressed genes (DEGs ...
Basiru Olaitan Ajiboye +7 more
doaj +2 more sources
Fimasartan, an angiotensin II receptor antagonist, ameliorates an in vivo zebrafish model of heart failure [PDF]
Background/Aims Angiotensin II in the failing heart initially helps to maintain cardiac output and blood pressure, but ultimately accelerates its deterioration.
Hailian Quan +3 more
doaj +1 more source
Ovarian cancer is one of the most lethal gynecological malignancies. Recurrence or acquired chemoresistance is the leading cause of ovarian cancer therapy failure.
Wei Huang +10 more
doaj +1 more source

