
Journal of Computer-Aided Molecular Design, Journal Year: 2025, Volume and Issue: 39(1)
Published: April 23, 2025
Language: Английский
Journal of Computer-Aided Molecular Design, Journal Year: 2025, Volume and Issue: 39(1)
Published: April 23, 2025
Language: Английский
Antibiotics, Journal Year: 2024, Volume and Issue: 13(3), P. 257 - 257
Published: March 14, 2024
Acinetobacter baumannii is a Gram-negative pathogen responsible for variety of community- and hospital-acquired infections. It recognized as life-threatening among hospitalized individuals and, in particular, immunocompromised patients many countries. A. baumannii, member the ESKAPE group, encompasses high genomic plasticity simultaneously predisposed to receive exchange mobile genetic elements (MGEs) through horizontal transfer (HGT). Indeed, treasure trove that contains number virulence factors. In accordance with these unique pathogenic characteristics authors aim discuss natural pan-genome factors pertaining this bacterial monster try highlight reasons why bacterium great concern global public health system.
Language: Английский
Citations
25Biomedicines, Journal Year: 2024, Volume and Issue: 12(2), P. 297 - 297
Published: Jan. 27, 2024
This review comprehensively explores the intricate landscape of anaplastic lymphoma kinase (ALK), focusing specifically on its pivotal role in non-small cell lung cancer (NSCLC). Tracing ALK's discovery, from fusion with nucleolar phosphoprotein (NPM)-1 large non-Hodgkin's (ALCL) 1994, elucidates subsequent impact ALK gene alterations various malignancies, including inflammatory myofibroblastoma and NSCLC. Approximately 3-5% NSCLC patients exhibit complex rearrangements, leading to approval six ALK-tyrosine inhibitors (TKIs) by 2022, revolutionizing treatment for advanced metastatic + Notably, second-generation TKIs such as alectinib, ceritinib, brigatinib have emerged address resistance issues initially associated pioneer ALK-TKI, crizotinib.
Language: Английский
Citations
17Heliyon, Journal Year: 2025, Volume and Issue: 11(4), P. e42509 - e42509
Published: Feb. 1, 2025
:Extracellular vesicles (EVs), are critical mediators of intercellular communication and exhibit significant potential across various biomedical domains. These nano-sized, membrane-encapsulated entities have captured substantial interest due to their diverse roles in pathogenesis promising therapeutic applications. EVs manage numerous physiological processes by transferring bioactive molecules, including proteins, lipids, nucleic acids, between cells. This review delves into the factors influencing properties EVs, such as temperature stress conditions, which collectively influence size, composition, functional attributes. We also describe emerging emphasizing involvement microbial interactions, immune modulation, antimicrobial resistance spread innovative diagnostic instruments. Despite applications, advancement EV-based therapies faces several challenges, will be discussed. By elucidating these elements, we aim provide a comprehensive overview transformative revolutionizing diagnostics therapeutics medicine.
Language: Английский
Citations
4Frontiers in Immunology, Journal Year: 2024, Volume and Issue: 15
Published: May 16, 2024
Importance Research is beginning to elucidate the sophisticated mechanisms underlying microbiota-gut-brain-immune interface, moving from primarily animal models human studies. Findings support dynamic relationships between gut microbiota as an ecosystem (microbiome) within (host) and its intersection with host immune nervous systems. Adding this effects on epigenetic regulation of gene expression further complicates strengthens response. At heart inflammation, which manifests in a variety pathologies including neurodegenerative diseases such Alzheimer’s disease, Parkinson’s Multiple Sclerosis (MS). Observations Generally, research date limited has focused bacteria, likely due simplicity cost-effectiveness 16s rRNA sequencing, despite lower resolution inability determine functional ability/alterations. However, omits all other fungi, viruses, phages, are emerging key members microbiome. Much been done pre-clinical and/or small studies more developed parts world. The observed promising but cannot be considered reliable or generalizable at time. Specifically, causal determined currently. More followed by then little MS. data for MS encouraging this. Conclusions relevance While still nascent, interface may missing link, hampered our progress understanding, let alone preventing, managing, putting into remission diseases. Relationships must first established humans, have shown poorly translate complex physiology environments, especially when investigating microbiome where often overly simplistic. Only can robust conducted humans using mechanistic model
Language: Английский
Citations
9Cancer Letters, Journal Year: 2024, Volume and Issue: 598, P. 217116 - 217116
Published: July 14, 2024
Language: Английский
Citations
9Immunity Inflammation and Disease, Journal Year: 2024, Volume and Issue: 12(7)
Published: July 1, 2024
Abstract Background Toll‐like receptors (TLRs) are a family of fundamental pattern recognition in the innate immune system, constituting first line defense against endogenous and exogenous antigens. The gut microbiota, collection commensal microorganisms intestine, is major source components metabolites microbiota interact with specific TLRs to contribute whole‐body metabolic homeostasis. Objective This review aims summarize interaction between TLR signaling pathways enumerate role dysbiosis‐induced obesity, inflammatory bowel disease (IBD), colorectal cancer (CRC). Results Through TLRs, facilitates development both adaptive systems, while system monitors dynamic changes bacteria maintain balance host‐microorganism symbiosis. Dysbiosis can induce cascade responses mediated by pathways, potentially resulting various diseases. Conclusion Understanding crosstalk contributes potential therapeutic applications related diseases, offering new avenues for treatment strategies conditions like IBD, CRC.
Language: Английский
Citations
9Cellular and Molecular Life Sciences, Journal Year: 2024, Volume and Issue: 81(1)
Published: Oct. 30, 2024
Language: Английский
Citations
9Frontiers in Immunology, Journal Year: 2023, Volume and Issue: 14
Published: Oct. 9, 2023
EDITORIAL article Front. Immunol., 09 October 2023Sec. Molecular Innate Immunity Volume 14 - 2023 | https://doi.org/10.3389/fimmu.2023.1294869
Language: Английский
Citations
15Frontiers in Endocrinology, Journal Year: 2024, Volume and Issue: 14
Published: Jan. 8, 2024
Gonadotropin-releasing hormone (GnRH1) and its receptor (GnRHR1) drive reproduction by regulating gonadotropins. Another form, GnRH2, (GnRHR2), also exist in mammals. In humans, GnRH2 GnRHR2 genes are present, but coding errors the gene predicted to hinder full-length protein production. Nonetheless, mounting evidence supports presence of a functional humans. have been identified throughout body, including peripheral reproductive tissues like ovary, uterus, breast, prostate. addition, detected wide number cancer cells Notably, analogues potent anti-proliferative, pro-apoptotic, and/or anti-metastatic effects on various cancers, endometrial, placental, ovarian, Thus, is an emerging target treat human cancers.
Language: Английский
Citations
5International Journal of Molecular Sciences, Journal Year: 2024, Volume and Issue: 25(6), P. 3105 - 3105
Published: March 7, 2024
Tumors intricately shape a highly immunosuppressive microenvironment, hampering effective antitumor immune responses through diverse mechanisms. Consequently, achieving optimal efficacy in cancer immunotherapy necessitates the reorganization of tumor microenvironment and restoration responses. Bladder cancer, ranking as second most prevalent malignant urinary tract, presents formidable challenge. Immunotherapeutic interventions including intravesical BCG checkpoint inhibitors such atezolizumab, avelumab, pembrolizumab have been implemented. However, substantial unmet need persists majority bladder patients across all stages do not respond adequately to immunotherapy. establishes that can actively hinder an efficient anti-tumor response. A deeper understanding evasion mechanisms will aid suppressing recurrence identifying viable therapeutic targets. This review seeks elucidate specific explore novel pathways molecular targets might circumvent resistance
Language: Английский
Citations
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