keyword
https://read.qxmd.com/read/38493149/casein-kinase-2-phosphorylates-and-induces-the-sall2-tumor-suppressor-degradation-in-colon-cancer-cells
#21
JOURNAL ARTICLE
V E Hermosilla, L Gyenis, A J Rabalski, M E Armijo, P Sepúlveda, F Duprat, D Benítez-Riquelme, F Fuentes-Villalobos, A Quiroz, M I Hepp, C Farkas, M Mastel, I González-Chavarría, R Jackstadt, D W Litchfield, A F Castro, R Pincheira
Spalt-like proteins are Zinc finger transcription factors from Caenorhabditis elegans to vertebrates, with critical roles in development. In vertebrates, four paralogues have been identified (SALL1-4), and SALL2 is the family's most dissimilar member. SALL2 is required during brain and eye development. It is downregulated in cancer and acts as a tumor suppressor, promoting cell cycle arrest and cell death. Despite its critical functions, information about SALL2 regulation is scarce. Public data indicate that SALL2 is ubiquitinated and phosphorylated in several residues along the protein, but the mechanisms, biological consequences, and enzymes responsible for these modifications remain unknown...
March 16, 2024: Cell Death & Disease
https://read.qxmd.com/read/38489888/moracin-d-suppresses-cell-growth-and-induces-apoptosis-via-targeting-the-xiap-parp1-axis-in-pancreatic-cancer
#22
JOURNAL ARTICLE
Xi Zhong, Xiaoxue Ke, He Yang, Xiang Ye, Can Li, Jun Pan, Wenhao Ran, Feng Wang, Hongjuan Cui
BACKGROUND: Pancreatic cancer, a tumor with a high metastasis rate and poor prognosis, is among the deadliest human malignancies. Investigating effective drugs for their treatment is imperative. Moracin D, a natural benzofuran compound isolated from Morus alba L., shows anti-inflammation and anti-breast cancer properties and is effective against Alzheimer's disease. However, the effect and mechanism of Moracin D action in pancreatic cancer remain obscure. PURPOSE: To investigate the function and molecular mechanism of Moracin D action in repressing the malignant progression of pancreatic cancer...
March 11, 2024: Phytomedicine
https://read.qxmd.com/read/38488146/covalent-fragment-screening-and-optimization-identifies-the-chloroacetohydrazide-scaffold-as-inhibitors-for-ubiquitin-c-terminal-hydrolase-l1
#23
JOURNAL ARTICLE
Ryan D Imhoff, Rishi Patel, Muhammad Hassan Safdar, Hannah B L Jones, Adan Pinto-Fernandez, Iolanda Vendrell, Hao Chen, Christine S Muli, Aaron D Krabill, Benedikt M Kessler, Michael K Wendt, Chittaranjan Das, Daniel P Flaherty
Dysregulation of the ubiquitin-proteasome systems is a hallmark of various disease states including neurodegenerative diseases and cancer. Ubiquitin C-terminal hydrolase L1 (UCHL1), a deubiquitinating enzyme, is expressed primarily in the central nervous system under normal physiological conditions, however, is considered an oncogene in various cancers, including melanoma, lung, breast, and lymphoma. Thus, UCHL1 inhibitors could serve as a viable treatment strategy against these aggressive cancers. Herein, we describe a covalent fragment screen that identified the chloroacetohydrazide scaffold as a covalent UCHL1 inhibitor...
March 15, 2024: Journal of Medicinal Chemistry
https://read.qxmd.com/read/38480493/arginine-selective-bioconjugation-reagent-for-effective-18-f-labeling-of-native-proteins
#24
JOURNAL ARTICLE
Pragalath Sadasivam, Shivashankar Khanapur, Siddesh V Hartimath, Boominathan Ramasamy, Peter Cheng, Chin Zan Feng, David Green, Christopher Davis, Julian L Goggi, Edward G Robins, Ran Yan
Protein-based 18 F-PET tracers offer new possibilities in early disease detection and personalized medicine. Their development relies heavily on the availability and effectiveness of 18 F-prosthetic groups. We prepared and evaluated a novel arginine-selective prosthetic group, 4-[18 F]fluorophenylglyoxal ([18 F]FPG). [18 F]FPG was radiosynthesized by a one-pot, two-step procedure with a non-decay-corrected (n.d.c.) isolated radiochemical yield (RCY) of 41 ± 8% ( n = 10). [18 F]FPG constitutes a generic tool for 18 F-labeling of various proteins, including human serum albumin (HSA), ubiquitin, interleukin-2, and interleukin-4 in ∼30-60% n...
March 13, 2024: Journal of Medicinal Chemistry
https://read.qxmd.com/read/38479223/inhibition-of-glycogen-synthase-kinase-3-enhances-nrf2-protein-stability-nuclear-localisation-and-target-gene-transcription-in-pancreatic-beta-cells
#25
JOURNAL ARTICLE
Chinmai Patibandla, Lidy van Aalten, Albena T Dinkova-Kostova, Tadashi Honda, Antonio Cuadrado, Raquel Fernández-Ginés, Alison D McNeilly, John D Hayes, James Cantley, Calum Sutherland
Accumulation of reactive oxygen species (i.e., oxidative stress) is a leading cause of beta cell dysfunction and apoptosis in diabetes. NRF2 (NF-E2 p45-related factor-2) regulates the adaptation to oxidative stress, and its activity is negatively regulated by the redox-sensitive CUL3 (cullin-3) ubiquitin ligase substrate adaptor KEAP1 (Kelch-like ECH-associated protein-1). Additionally, NRF2 is repressed by the insulin-regulated Glycogen Synthase Kinase-3 (GSK3). We have demonstrated that phosphorylation of NRF2 by GSK3 enhances β-TrCP (beta-transducin repeat-containing protein) binding and ubiquitylation by CUL1 (cullin-1), resulting in increased proteasomal degradation of NRF2...
March 7, 2024: Redox Biology
https://read.qxmd.com/read/38474037/protein-kinase-d-plays-a-crucial-role-in-maintaining-cardiac-homeostasis-by-regulating-post-translational-modifications-of-myofilament-proteins
#26
JOURNAL ARTICLE
Melissa Herwig, Merima Begovic, Heidi Budde, Simin Delalat, Saltanat Zhazykbayeva, Marcel Sieme, Luca Schneider, Kornelia Jaquet, Andreas Mügge, Ibrahim Akin, Ibrahim El-Battrawy, Jens Fielitz, Nazha Hamdani
Protein kinase D (PKD) enzymes play important roles in regulating myocardial contraction, hypertrophy, and remodeling. One of the proteins phosphorylated by PKD is titin, which is involved in myofilament function. In this study, we aimed to investigate the role of PKD in cardiomyocyte function under conditions of oxidative stress. To do this, we used mice with a cardiomyocyte-specific knock-out of Prkd1, which encodes PKD1 (Prkd1loxP/loxP ; αMHC-Cre ; PKD1 cKO), as well as wild type littermate controls (Prkd1loxP/loxP ; WT)...
February 28, 2024: International Journal of Molecular Sciences
https://read.qxmd.com/read/38471041/downregulation-of-endogenous-nectin1-in-human-keratinocytes-by-herpes-simplex-virus-1-glycoprotein-d-excludes-superinfection-but-does-not-affect-nk-cell-function
#27
JOURNAL ARTICLE
Joanne Kite, Monica Hill, Natasha Preston, Anzelika Rubina, Simon Kollnberger, Eddie Chung Yern Wang, Gillian Elliott
Many viruses downregulate their cognate receptors, facilitating virus replication and pathogenesis via processes that are not yet fully understood. In the case of herpes simplex virus 1 (HSV1), the receptor binding protein glycoprotein D (gD) has been implicated in downregulation of its receptor nectin1, but current understanding of the process is limited. Some studies suggest that gD on the incoming virion is sufficient to achieve nectin1 downregulation, but the virus-encoded E3 ubiquitin ligase ICP0 has also been implicated...
March 2024: Journal of General Virology
https://read.qxmd.com/read/38469033/genetic-risk-for-hospitalization-of-african-american-patients-with-severe-mental-illness-reveals-hla-loci
#28
JOURNAL ARTICLE
Adriana Lori, Brad D Pearce, Seyma Katrinli, Sierra Carter, Charles F Gillespie, Bekh Bradley, Aliza P Wingo, Tanja Jovanovic, Vasiliki Michopoulos, Erica Duncan, Rebecca C Hinrichs, Alicia Smith, Kerry J Ressler
BACKGROUND: Mood disorders such as major depressive and bipolar disorders, along with posttraumatic stress disorder (PTSD), schizophrenia (SCZ), and other psychotic disorders, constitute serious mental illnesses (SMI) and often lead to inpatient psychiatric care for adults. Risk factors associated with increased hospitalization rate in SMI (H-SMI) are largely unknown but likely involve a combination of genetic, environmental, and socio-behavioral factors. We performed a genome-wide association study in an African American cohort to identify possible genes associated with hospitalization due to SMI (H-SMI)...
2024: Frontiers in Psychiatry
https://read.qxmd.com/read/38468948/repurposing-of-us-fda-approved-drugs-as-negative-modulators-of-ubiquitin-specific-protease-7-usp7
#29
JOURNAL ARTICLE
Seema Zadi, Sumaira Javaid, Atia-Tul-Wahab, Humaira Zafar, Muhammad Awais, Innokentiy Maslennikov, M Iqbal Choudhary
Ubiquitin-specific protease7 (USP7) regulates the stability of the p53 tumor suppressor protein and several other proteins critical for tumor cell survival. Aberrant expression of USP7 facilitates human malignancies by altering the activity of proto-oncogenes/proteins, and tumor suppressor genes. Therefore, USP7 is a validated anti-cancer drug target. In this study, a drug repurposing approach was used to identify new hits against the USP7 enzyme. It is one of the most strategic approaches to find new uses for drugs in a cost- and time-effective way...
March 15, 2024: Heliyon
https://read.qxmd.com/read/38465576/a-recurrent-missense-variant-in-the-e3-ubiquitin-ligase-substrate-recognition-subunit-fem1b-causes-a-rare-syndromic-neurodevelopmental-disorder
#30
JOURNAL ARTICLE
François Lecoquierre, A Mattijs Punt, Frédéric Ebstein, Ilse Wallaard, Rob Verhagen, Maja Studencka-Turski, Yannis Duffourd, Sébastien Moutton, Frédédic Tran Mau-Them, Christophe Philippe, John Dean, Stephen Tennant, Alice S Brooks, Marjon A van Slegtenhorst, Julie A Jurgens, Brenda J Barry, Wai-Man Chan, Eleina M England, Mayra Martinez Ojeda, Elizabeth C Engle, Caroline D Robson, Michelle Morrow, A Micheil Innes, Ryan Lamont, Matthea Sanderson, Elke Krüger, Christel Thauvin, Ben Distel, Laurence Faivre, Ype Elgersma, Antonio Vitobello
PURPOSE: FEM1B acts as a substrate recognition subunit for ubiquitin ligase complexes belonging to the CRL2 E3 family. Several biological functions have been proposed for FEM1B, including a structurally resolved function as a sensor for redox cell status by controlling mitochondrial activity, but its implication in human disease remains elusive. METHODS: To understand the involvement of FEM1B in human disease, we made use of Matchmaker exchange platforms to identify individuals with de novo variants in FEM1B and performed their clinical evaluation...
March 7, 2024: Genetics in Medicine: Official Journal of the American College of Medical Genetics
https://read.qxmd.com/read/38458410/overexpressing-of-the-gipc1-protects-against-pathological-cardiac-remodeling
#31
JOURNAL ARTICLE
Xi Sun, Yanna Han, Yahan Yu, Yujie Chen, Chaorun Dong, Yuan Lv, Huan Qu, Zheyu Fan, Yi Yu, Yaru Sang, Wenxia Tang, Yu Liu, Jiaming Ju, Dan Zhao, Yunlong Bai
OBJECTIVE: Pathological cardiac remodeling, including cardiac hypertrophy and fibrosis, is a key pathological process in the development of heart failure. However, effective therapeutic approaches are limited. The β-adrenergic receptors are pivotal signalling molecules in regulating cardiac function. G-alpha interacting protein (GAIP)-interacting protein, C-terminus 1 (GIPC1) is a multifunctional scaffold protein that directly binds to the C-terminus of β1-adrenergic receptor (β1-adrenergic receptor)...
March 6, 2024: European Journal of Pharmacology
https://read.qxmd.com/read/38458201/cdk-independent-role-of-d-type-cyclins-in-regulating-dna-mismatch-repair
#32
JOURNAL ARTICLE
Gergely Rona, Bearach Miwatani-Minter, Qingyue Zhang, Hailey V Goldberg, Marc A Kerzhnerman, Jesse B Howard, Daniele Simoneschi, Ethan Lane, John W Hobbs, Elizabeth Sassani, Andrew A Wang, Sarah Keegan, Daniel J Laverty, Cortt G Piett, Lorinc S Pongor, Miranda Li Xu, Joshua Andrade, Anish Thomas, Piotr Sicinski, Manor Askenazi, Beatrix Ueberheide, David Fenyö, Zachary D Nagel, Michele Pagano
Although mismatch repair (MMR) is essential for correcting DNA replication errors, it can also recognize other lesions, such as oxidized bases. In G0 and G1, MMR is kept in check through unknown mechanisms as it is error-prone during these cell cycle phases. We show that in mammalian cells, D-type cyclins are recruited to sites of oxidative DNA damage in a PCNA- and p21-dependent manner. D-type cyclins inhibit the proteasomal degradation of p21, which competes with MMR proteins for binding to PCNA, thereby inhibiting MMR...
February 29, 2024: Molecular Cell
https://read.qxmd.com/read/38452206/wsb1-2-target-chromatin-bound-lysine-methylated-rela-for-proteasomal-degradation-and-nf-%C3%AE%C2%BAb-termination
#33
JOURNAL ARTICLE
Jie Zhang, Yuanyuan Yu, Xiuqun Zou, Yaning Du, Qiankun Liang, Mengyao Gong, Yurong He, Junqi Luo, Dandan Wu, Xiaoli Jiang, Matt Sinclair, Emad Tajkhorshid, Hong-Zhuan Chen, Zhaoyuan Hou, Yuejuan Zheng, Lin-Feng Chen, Xiao-Dong Yang
Proteasome-mediated degradation of chromatin-bound NF-κB is critical in terminating the transcription of pro-inflammatory genes and can be triggered by Set9-mediated lysine methylation of the RelA subunit. However, the E3 ligase targeting methylated RelA remains unknown. Here, we find that two structurally similar substrate-recognizing components of Cullin-RING E3 ligases, WSB1 and WSB2, can recognize chromatin-bound methylated RelA for polyubiquitination and proteasomal degradation. We showed that WSB1/2 negatively regulated a subset of NF-κB target genes via associating with chromatin where they targeted methylated RelA for ubiquitination, facilitating the termination of NF-κB-dependent transcription...
March 7, 2024: Nucleic Acids Research
https://read.qxmd.com/read/38451783/activity-of-the-ubiquitin-activating-enzyme-inhibitor-tak-243-in-adrenocortical-carcinoma-acc-cell-lines-patient-derived-organoids-pdos-and-murine-xenografts
#34
JOURNAL ARTICLE
Yashuhiro Arakawa, Ukhyun Jo, Suresh Kumar, Nai-Yun Sun, Fathi Elloumi, Anish Thomas, Nitin Roper, Diana Grace Varghese, Naoko Takebe, Xiaohu Zhang, Michele Ceribelli, David O Holland, Erin Beck, Zina Itkin, Crystal McKnight, Kelli M Wilson, Jameson Travers, Carleen Klumpp-Thomas, Craig J Thomas, Chuong D Hoang, Jonathan M Hernandez, Jaydira Del Rivero, Yves Pommier
Current treatment options for metastatic adrenocortical carcinoma (ACC) have limited efficacy, despite the common use of mitotane and cytotoxic agents. This study aimed to identify novel therapeutic options for ACC. An extensive drug screen was conducted to identify compounds with potential activity against ACC cell lines. We further investigated the mechanism of action of the identified compound, TAK-243, its synergistic effects with current ACC therapeutics, and its efficacy in ACC models including patient-derived organoids and mouse xenografts...
March 7, 2024: Cancer Res Commun
https://read.qxmd.com/read/38447828/ubd-participated-in-neutrophilic-asthma-by-promoting-the-activation-of-il-17-signaling
#35
JOURNAL ARTICLE
Yuchun Liu, Kang Cheng, Meng Sun, Cong Ding, Tao Li, Yangyang Jia, Chengbo Wang, Xiangzhan Zhu, Xiaorui Song, Rui Jia, Qionglin Wang, Yaodong Zhang, Xiaomin Sun
Neutrophilic asthma is a persistent and severe inflammatory lung disease characterized by neutrophil activation and the mechanisms of which are not completely elucidated. Ubiquitin D (UBD) is a ubiquitin-like modifier participating in infections, immune responses, and tumorigenesis, while whether UBD involves in neutrophilic asthma needs further study. In this study, we initially found that UBD expression was significantly elevated and interleukin 17 (IL-17) signaling was enriched in the endobronchial biopsies of severe asthma along with neutrophils increasing by bioinformatics analysis...
March 4, 2024: International Journal of Biological Macromolecules
https://read.qxmd.com/read/38438582/brigatinib-a-newly-discovered-axl-inhibitor-suppresses-axl-mediated-acquired-resistance-to-osimertinib-in-egfr-mutated-non-small-cell-lung-cancer
#36
JOURNAL ARTICLE
Rui Han, Cong-Hua Lu, Chen Hu, Yuan-Yao Dou, Jun Kang, Cai-Yu Lin, Di Wu, Wei-Ling Jiang, Guo-Qing Yin, Yong He
In addition to the classical resistance mechanisms, receptor tyrosine-protein kinase AXL is a main mechanism of resistance to third-generation epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) osimertinib in EGFR-mutated non-small cell lung cancer (NSCLC). Developing an effective AXL inhibitor is important to sensitize osimertinib in clinical application. In this study we assessed the efficacy of brigatinib, a second-generation of anaplastic lymphoma kinase (ALK)-TKI, as a novel AXL inhibitor, in overcoming acquired resistance to osimertinib induced by AXL activation...
March 4, 2024: Acta Pharmacologica Sinica
https://read.qxmd.com/read/38424059/generation-of-g51d-and-3d-mice-reveals-decreased-%C3%AE-synuclein-tetramer-monomer-ratios-promote-parkinson-s-disease-phenotypes
#37
JOURNAL ARTICLE
Silke Nuber, Xiaoqun Zhang, Thomas D McCaffery, Tim E Moors, Marie-Alexandre Adom, Wolf N Hahn, Dylan Martin, Maria Ericsson, Arathi Tripathi, Ulf Dettmer, Per Svenningsson, Dennis J Selkoe
Mutations in the α-Synuclein (αS) gene promote αS monomer aggregation that causes neurodegeneration in familial Parkinson's disease (fPD). However, most mouse models expressing single-mutant αS transgenes develop neuronal aggregates very slowly, and few have dopaminergic cell loss, both key characteristics of PD. To accelerate neurotoxic aggregation, we previously generated fPD αS E46K mutant mice with rationally designed triple mutations based on the α-helical repeat motif structure of αS (fPD E46K→3 K)...
February 29, 2024: NPJ Parkinson's Disease
https://read.qxmd.com/read/38418820/mirror-image-ligand-discovery-enabled-by-single-shot-fast-flow-synthesis-of-d-proteins
#38
JOURNAL ARTICLE
Alex J Callahan, Satish Gandhesiri, Tara L Travaline, Rahi M Reja, Lia Lozano Salazar, Stephanie Hanna, Yen-Chun Lee, Kunhua Li, Olena S Tokareva, Jean-Marie Swiecicki, Andrei Loas, Gregory L Verdine, John H McGee, Bradley L Pentelute
Widespread adoption of mirror-image biological systems presents difficulties in accessing the requisite D-protein substrates. In particular, mirror-image phage display has the potential for high-throughput generation of biologically stable macrocyclic D-peptide binders with potentially unique recognition modes but is hindered by the individualized optimization required for D-protein chemical synthesis. We demonstrate a general mirror-image phage display pipeline that utilizes automated flow peptide synthesis to prepare D-proteins in a single run...
February 28, 2024: Nature Communications
https://read.qxmd.com/read/38401179/atf6-protects-against-protein-misfolding-during-cardiac-hypertrophy
#39
JOURNAL ARTICLE
Christoph Hofmann, Marjan Aghajani, Cecily D Alcock, Erik A Blackwood, Clara Sandmann, Nicole Herzog, Julia Groß, Lars Plate, R Luke Wiseman, Randal J Kaufman, Hugo A Katus, Tobias Jakobi, Mirko Völkers, Christopher C Glembotski, Shirin Doroudgar
Cardiomyocytes activate the unfolded protein response (UPR) transcription factor ATF6 during pressure overload-induced hypertrophic growth. The UPR is thought to increase ER protein folding capacity and maintain proteostasis. ATF6 deficiency during pressure overload leads to heart failure, suggesting that ATF6 protects against myocardial dysfunction by preventing protein misfolding. However, conclusive evidence that ATF6 prevents toxic protein misfolding during cardiac hypertrophy is still pending. Here, we found that activation of the UPR, including ATF6, is a common response to pathological cardiac hypertrophy in mice...
February 23, 2024: Journal of Molecular and Cellular Cardiology
https://read.qxmd.com/read/38395768/genome-assembly-of-medicago-truncatula-accession-sa27063-provides-insight-into-spring-black-stem-and-leaf-spot-disease-resistance
#40
JOURNAL ARTICLE
Jacob R Botkin, Andrew D Farmer, Nevin D Young, Shaun J Curtin
Medicago truncatula, model legume and alfalfa relative, has served as an essential resource for advancing our understanding of legume physiology, functional genetics, and crop improvement traits. Necrotrophic fungus, Ascochyta medicaginicola, the causal agent of spring black stem (SBS) and leaf spot is a devasting foliar disease of alfalfa affecting stand survival, yield, and forage quality. Host resistance to SBS disease is poorly understood, and control methods rely on cultural practices. Resistance has been observed in M...
February 23, 2024: BMC Genomics
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