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Gecko proteins have long been used as anti-tumor agents in oriental medicine, without any scientific background. Although anti-tumor effects of Gecko proteins on several cancers were recently reported, their effect on bladder cancer has not been investigated. Thus, we explored the anti-tumor effect of Gecko proteins and its cellular mechanisms in human bladder cancer 5637 cells. Gecko proteins significantly reduced the viability of 5637 cells without any cytotoxic effect on normal cells. These proteins increased the Annexin-V staining and the amount of condensed chromatin, demonstrating that the Gecko proteinsinduced cell death was caused by apoptosis. Gecko proteins suppressed Akt activation, and the overexpression of constitutively active form of myristoylated Akt prevented Gecko proteins-induced death of 5637 cells. Furthermore, Gecko proteins activated caspase 9 and caspase 3/7. Taken together, our data demonstrated that Gecko proteins suppressed the Akt pathway and activated the intrinsic caspase pathway, leading to the apoptosis of bladder cancer cells. [BMB Reports 2015; 48(9): 531-536].
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http://dx.doi.org/10.5483/bmbrep.2015.48.9.117 | DOI Listing |
Pathogens
July 2025
Clinic for Birds and Reptiles, Leipzig University, 04103 Leipzig, Germany.
and have previously been described as pathogens causing hyalohyphomycosis in various species of captive chameleons and bearded dragons (). Previous studies yielded different genotypes of and based on sequencing of the internal transcribed spacer 1-5.8S rDNA (ITS-1-5.
View Article and Find Full Text PDFProc Biol Sci
August 2025
Department of Biomedical Sciences, Colorado State University, Fort Collins, CO 80523, USA.
Oxidative metabolism meets the majority of vertebrate energy demands through the coupling of mitochondrial respiration to ATP production (OXPHOS). In endotherms, variations in OXPHOS coupling efficiency influence metabolic thermogenesis, locomotor economy and reactive oxygen species (ROS) generation. However, the extent of these variations and their functional implications in ectotherms are less clear.
View Article and Find Full Text PDFEcol Evol
August 2025
Department of Earth and Environmental Sciences University of Pavia, Università degli Studi di Pavia Pavia Italy.
Among the modalities of animal communication, the chemical channel is the only one that allows signalers and receivers to communicate without being necessarily in the same place at the same time. This asynchrony may influence signal design, as its effectiveness depends on adapting to predictable environmental conditions. Many lizard species scent-mark territories by depositing waxy secretions made of protein-lipid mixtures from specialized epidermal glands.
View Article and Find Full Text PDFJ Exp Zool B Mol Dev Evol
August 2025
Laboratorio de Biología Reproductiva de Vertebrados, Grupo de Estudios en Biodiversidad, Universidad Industrial de Santander, Bucaramanga, Colombia.
In vertebrates, the provision of nutrients to developing embryos varies widely, ranging from yolk-dependent strategies to highly specialized forms of placental nourishment. Vitellogenins (VTGs) are essential proteins for egg yolk formation in oviparous and lecithotrophic species. In contrast, in eutherian mammals, the loss of VTGs is associated with the evolution of matrotrophy (placentotrophy and lactation), where maternal nutrition via the placenta replaces the need for large yolk reserves during embryonic development.
View Article and Find Full Text PDFInt J Mol Sci
August 2025
Adaptive Biotoxicology Lab, School of the Environment, University of Queensland, St Lucia, QLD 4072, Australia.
Many vertebrates have evolved resistance to snake venom as a result of coevolutionary chemical arms races. In Australian skinks (family Scincidae), who often encounter venomous elapid snakes, the frequency, diversity, and molecular basis of venom resistance have been unexplored. This study investigated the evolution of neurotoxin resistance in Australian skinks, focusing on mutations in the muscle nicotinic acetylcholine receptor (nAChR) α1 subunit's orthosteric site that prevent pathophysiological binding by α-neurotoxins.
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