Abstract Purpose: We investigated whether blockage the Transforming growth factor (TGF)-ß signaling ameliorated established liver radiation-induced liver fibrosis (RILF). Materials and Methods: A replication-defective adenoviral vector expressing the extracellular portion of mouse TßRII and the Fc portion of human immunoglobulin IgG fusion protein(AdT RIIFc) was produced. The entire liver was exposed to 30 Gy irradiation to generate a RILF model (RILFM). Then, RILFM animals were treated with AdT RIIFc (1× 1011 PFU, TßRII), Control virus (1×1011 PFU, AdGFP), or saline (SALIN). Delayed radiation liver injury was assessed using histology, morphometry, and immunohistochemistry. Chronic oxidative stress damage, hepatic stellate cell (HSC) activation, and hepatocyte regeneration were also analyzed. Results: Blocking TGF-ß signaling with AdT RIIFc successfully mitigated established radiation induced liver fibrosis (RILF). Compared with RILFM or AdGFP rats, AdT RIIFc-treated mice exhibited less oxidative stress damage, less HSC activation, preserved liver function. Conclusions: Modulation of TGF-ß with AdT RIIFc is feasible and ameliorates established radiation-induced liver fibrosis. These data confirm the putative role of TGF-ß in delayed radiation-induced liver damage. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 101st Annual Meeting of the American Association for Cancer Research; 2010 Apr 17-21; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2010;70(8 Suppl):Abstract nr LB-208.
SO 2- 4-TiO 2 solid superacid was used as catalyst in the alkylation of naphthalene with propylene to yield isopropylnaphthalene. The process is simple, lacking pollution and erosion. The optimal conditions of SO 2- 4-TiO 2 solid superacid are dipping acid concentration at 0.50?mol/L and calcinations temperature at 500?℃. The solid superacid can be used as catalyst two times in the alkylation of naphthalene, and the total composition of MIPN,DIPN, and TIPN in product is over 98%. When the consumption of catalyst is 10%, the temperature is 160?℃; the reaction time is 2.5?h.
One-dimensional Pt nanothorns are synthesized via a unique air/water interfacial process and anchored in situ densely on the surface of the supported CNTs film, which show efficient electrocatalytic ability for methanol oxidation.
Lung cancer stands as the leading cause of global cancer-related mortality, resulting in an approximate annual toll of 1.6 million lives.1Siegel R.L. Miller K.D. Wagle N.S. Jemal A. Cancer statistics, 2023.CA A Cancer J. Clin. 2023; 73: 17-48Crossref PubMed Scopus (1119) Google Scholar Within this context, non-small cell lung cancer (NSCLC) comprises about 85% of cases, encompassing a range of histological subtypes.2Petrella F. Rizzo S. Attili I. Passaro A. Zilli T. Martucci F. Bonomo L. Del Grande F. Casiraghi M. De Marinis F. Spaggiari L. Stage III Non-Small-Cell Lung Cancer: An Overview of Treatment Options.Curr. Oncol. 2023; 30: 3160-3175Crossref PubMed Scopus (2) Google Scholar Given the intricate genetic modifications underlying the emergence and progression of NSCLC, extensive gene expression profiling has pinpointed a multitude of dysregulated genes.3Rotow J. Bivona T.G. Understanding and targeting resistance mechanisms in NSCLC.Nat. Rev. Cancer. 2017; 17: 637-658Crossref PubMed Scopus (571) Google Scholar These discoveries have significantly informed clinical prognostications and predictions of therapeutic responsiveness. An array of mechanisms, including exon deletion, copy-number variation, and epigenetic modification, have been linked to the disruption of gene expression profiles, as demonstrated by numerous studies.4Xue Y. Hou S. Ji H. Han X. Evolution from genetics to phenotype: reinterpretation of NSCLC plasticity, heterogeneity, and drug resistance.Protein Cell. 2017; 8: 178-190Crossref PubMed Scopus (16) Google Scholar Nonetheless, the comprehensive understanding of the driving forces behind gene expression dysregulation in NSCLC remains an ongoing pursuit. Alternative polyadenylation (APA) has been identified as one of the drivers of aberrant gene expression. Extensive APA events were found in multiple cancer types, which could regulate the expression of oncogenes and tumor suppressors. Accumulated evidence indicates that many APA events are cancer-type and cell-state specific. In a recent issue of Molecular Therapy – Nucleic Acids, Huang et al. describe the identification of heterogeneity of alternative polyadenylation events that occurs in multiple cell types by using bioinformatics pipeline and cell line experiments.5Huang K. Zhang Y. Shi X. Yin Z. Zhao W. Huang L. Wang F. Zhou X. Cell-type specific alternative polyadenylation promotes oncogenic gene expression in non-small cell lung cancer progression.Mol. Ther. Nucleic Acids. 2023; 33: 816-831Abstract Full Text Full Text PDF PubMed Scopus (0) Google Scholar In the current study, Huang et al. collected single-cell RNA sequencing data from previously published studies. Then, the authors systematically analyzed APA events in over 40,000 cells, identifying broadly dysregulated APA events across seven distinct cell types. To ascertain the potential implications of these APA events, the authors pinpointed the loss of microRNA (miRNA)-binding sites resulting from shortened 3′ UTRs, as well as the influence of APA-mediated miRNA regulation. Furthermore, the authors discerned the functional significance of APA-associated genes and validated their roles in cancer cell migration and metastasis. In a bid to explore potential interactions with APA-related genes, the authors conducted drug sensitivity tests on lung cancer cell lines using the Genomics of Drug Sensitivity in Cancer (GDSC) database (Figure 1). According to the analyses, Huang et al. identified widespread APA events in NSCLC across various cell types. Among these events, many are specific to certain cell types and regulate the expression of oncogenes. For instance, the authors noted significant upregulation of eight genes in four distinct cell types in NSCLC samples: SPARC, RGS5, and CD59 in cancer-associated fibroblasts (CAFs), IL1RN in myeloid cells, TMBIM6 in alveolar cells, and RPL22, DERL1, and HM13 in B cells. Notably, the expression of SPARC displayed a robust correlation with patient prognosis. Subsequently, the authors explored the patterns of miRNA-binding site loss induced by APA events in these seven cell types. Prior research had already highlighted the loss of multiple miRNA-binding sites due to APA events. In line with these findings, the authors revealed the widespread occurrence of miRNA-binding site loss in genes affected by APA events. As an example, both bioinformatic analysis and experiments demonstrated the loss of the miR-203a-3p.1-binding site due to APA events in SPARC. It was also shown that miR-203a-3p.1 significantly suppressed the expression of SPARC. Furthermore, the evasion of miR-203a-3p.1 led to the inhibition of tumor-suppressor genes SOCS3 and ETS2. Additionally, the authors uncovered interactions between SPARC and genes regulated by epithelial-mesenchymal transition (EMT), such as COL1A1, TGFBR2, and VCAM1. These interactions are strongly correlated with cancer progression and metastasis. The study then confirmed the role of SPARC in lung cancer proliferation and migration through experiments involving SPARC knockdown cell lines. Drug response analysis also revealed that patients with high SPARC expression levels displayed greater sensitivity to cisplatin treatment compared with the low-SPARC-expression group. Therefore, the analysis suggested that patients with high SPARC expression might derive more benefits from cisplatin treatment. The innovation of cell-type-specific APA represents a significant advancement in the field of NSCLC. Currently, our understanding of dynamic APA regulation in different cell types remains rudimentary. The heterogeneity of APA in distinct cell types may yield valuable insights into the mechanisms of carcinogenesis, progression, and metastasis. While SPARC has been extensively studied in various cancer cell lines, its role in tumorigenesis remains controversial due to its highly cell-type-specific functions.6Arnold S.A. Brekken R.A. SPARC: a matricellular regulator of tumorigenesis.J. Cell Commun. Signal. 2009; 3: 255-273Crossref PubMed Scopus (131) Google Scholar A previous study demonstrated that the low expression of SPARC in lung cancer cells results from its aberrant methylation.7Suzuki M. Hao C. Takahashi T. Shigematsu H. Shivapurkar N. Sathyanarayana U.G. Iizasa T. Fujisawa T. Hiroshima K. Gazdar A.F. Aberrant methylation of SPARC in human lung cancers.Br. J. Cancer. 2005; 92: 942-948Crossref PubMed Scopus (62) Google Scholar However, the cell-type-specific function of SPARC in NSCLC remains unknown. This study not only broadens our understanding of the underlying biological mechanisms of NSCLC but also identifies potential targets for predicting the response to cisplatin treatment in patients with NSCLC. Future research should aim to optimize the therapeutic potential of SPARC in CAFs, uncover its response to other therapies, and comprehensively assess its efficacy as a drug target in mouse models and preclinical trials. In conclusion, this study provides novel insights into the mechanisms underpinning drug resistance in patients with NSCLC. All authors actively contributed to the writing of this commentary. The authors declare no competing interests.
Alzheimer's disease (AD) is the most common form of dementia, affecting millions of people worldwide. Increasing evidence suggests that formaldehyde might be one of the various pathological mechanisms involved in the process of AD onset. Here, we use
Owing to its high mortality rate, lung cancer (LC) remains the most common cancer worldwide, with the highest malignancy diagnosis rate. The phosphatidylinositol-3-kinase (PI3K)/protein kinase B (AKT)/mammalian target of rapamycin (mTOR) signaling (PAM) pathway is a critical intracellular pathway involved in various cellular functions and regulates numerous cellular processes, including growth, survival, proliferation, metabolism, apoptosis, invasion, and angiogenesis. This review aims to highlight preclinical and clinical studies focusing on the PAM signaling pathway in LC and underscore the potential of natural products targeting it. Additionally, this review synthesizes the existing literature and discusses combination therapy and future directions for LC treatment while acknowledging the ongoing challenges in the field. Continuous development of novel therapeutic agents, technologies, and precision medicine offers an increasingly optimistic outlook for the treatment of LC.
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