A practice-oriented genome-profiling study for acute myeloid leukemia using the novel HANDLE system: HM-screen-JAPAN02.

HM-SCREEN-Japan is a multicenter collaborative project in Japan to evaluate the clinical utility of a cancer genome panel in the treatment of acute myeloid leukemia (AML). The HM-SCREEN-JAPAN02 study used the Amoy Myeloid Panel with the HANDLE system, which enables efficient and rapid sequencing, as the genomic testing kit. The Amoy Myeloid Panel targets 53 genes with established clinical significance or high prevalence.

Layer-by-Layer-Assembled Polyaniline/MXene Thin Film and Device for Improved Electrochromic and Energy Storage Capabilities.

Polyaniline (PANI) is an attractive electrochromic and storage material due to its reversible and sustainable electrochemical redox processes. However, the insufficient surface area and excessive charge intercalation after long-term cycling results in limited charge capacitance and unsatisfactory cycling stability. In this work, we demonstrate an innovative method to increase PANI's electrochromic and energy storage performance by incorporating MXene, to enhance electrochemical activity and reveal more active areas of ion/electron intercalation/deintercalation and charge transfer.

Anticoagulation Patterns in Ischemic Stroke Patients with Atrial Fibrillation in Developing Country: Insights from the Stroke Registry in Vietnam.

(1) Background: Atrial fibrillation (AF) poses a growing cardiovascular challenge globally, with significant implications in Vietnam. This study aimed to investigate the impact of AF on ischemic stroke/transient ischemic attack (TIA) and clinical outcomes, as well as the utilization of oral anticoagulation (OAC) therapy in Vietnam. (2) Methods: Data from the Registry of Stroke Care Quality (RES-Q) across 66 hospitals in Vietnam between 2017 and 2023 were utilized.

Nivolumab Plus 5-Azacitidine in Pediatric Relapsed/Refractory Acute Myeloid Leukemia (AML): Phase I/II Trial Results from the Therapeutic Advances in Childhood Leukemia and Lymphoma (TACL) Consortium.

Improvements in survival have been made over the past two decades for childhood acute myeloid leukemia (AML), but the approximately 40% of patients who relapse continue to have poor outcomes. A combination of checkpoint-inhibitor nivolumab and azacitidine has demonstrated improvements in median survival in adults with AML. This phase I/II study with nivolumab and azacitidine in children with relapsed/refractory AML (NCT03825367) was conducted through the Therapeutic Advances in Childhood Leukemia & Lymphoma consortium.

Dynamically Reversible Interconversion of Molecular Catalysts for Efficient Electrooxidation of Propylene into Propylene Glycol.

For the electrooxidation of propylene into 1,2-propylene glycol (PG), the process involves two key steps of the generation of *OH and the transfer of *OH to the C═C bond in propylene. The strong *OH binding energy ((*OH)) favors the dissociation of HO into *OH, whereas the transfer of *OH to propylene will be impeded. The scaling relationship of the (*OH) plays a key role in affecting the catalytic performance toward propylene electrooxidation.

Combined PD-1, BRAF and MEK inhibition in BRAF colorectal cancer: a phase 2 trial.

While BRAF inhibitor combinations with EGFR and/or MEK inhibitors have improved clinical efficacy in BRAF colorectal cancer (CRC), response rates remain low and lack durability. Preclinical data suggest that BRAF/MAPK pathway inhibition may augment the tumor immune response. We performed a proof-of-concept single-arm phase 2 clinical trial of combined PD-1, BRAF and MEK inhibition with sparatlizumab (PDR001), dabrafenib and trametinib in 37 patients with BRAF CRC.

The Synthesis, Characterization and Anti-Tumor Activity of a Cu-MOF Based on Flavone-6,2'-dicarboxylic Acid.

A novel two-dimensional copper(II) framework (LDU-1), formulated as {[Cu(L)·2NMP}n (HL = flavone-6,2'-dicarboxylic acid, NMP = N-Methyl pyrrolidone), has been constructed under solvothermal conditions and characterized by single-crystal X-ray diffraction, infrared spectroscopy (IR), thermogravimetric analysis and powder X-ray diffraction (PXRD). In the crystal structure, the Cu(II) shows hex-coordinated with the classical Cu paddle-wheel coordination geometry, and the flavonoid ligand coordinates with the Cu(II) ion in a bidentate bridging mode. Of particular interest of LDU-1 is the presence of anti-tumor activity against three human cancer cell lines including lung adenocarcinoma(A549), Michigan cancer foundation-7 (MCF-7), erythroleukemia (K562) and murine melanoma B16F10, indicating synergistic enhancement effects between metal ions and organic linkers.

Metric-Based Assessment Method for MS-T Formalism with Small Subsets of Torsional Conformers.

The multi-structural approximation with torsional anharmonicity (MS-T) method and its variants have been widely used for calculating conformational-rovibrational partition functions of large molecules. The present work aimed to propose a systematic method to assess and explain the performance of various variants of the MS-T method. First, we proposed the simplest variant MS-T(2NN) (two nearest neighborhood torsions are coupled) and systematically validated it for large alkanes -CH ( = 6-10) and their transition states of hydrogen abstraction reactions.

The AUTOTAC chemical biology platform for targeted protein degradation via the autophagy-lysosome system.

Targeted protein degradation allows targeting undruggable proteins for therapeutic applications as well as eliminating proteins of interest for research purposes. While several degraders that harness the proteasome or the lysosome have been developed, a technology that simultaneously degrades targets and accelerates cellular autophagic flux is still missing. In this study, we develop a general chemical tool and platform technology termed AUTOphagy-TArgeting Chimera (AUTOTAC), which employs bifunctional molecules composed of target-binding ligands linked to autophagy-targeting ligands.

Rearrangement of Ion Transport Path on Nano-Cross-linker for All-Solid-State Electrolyte with High Room Temperature Ionic Conductivity.

The low room temperature ionic conductivity (RTσ) of polyethylene oxide (PEO)-based solid-state polymer electrolyte (SPE) severely restricts its application for lithium batteries. Herein, acrylamide (AM) has been introduced into the poly(ethylene glycol) methyl ether methacrylate-poly(ethylene glycol) diacrylate (P-P). The multiple hydrogen bonds of AM expand the original single lithium environment (Li···O-C) to three types (Li···O-C, Li···N-H, and Li···O═C), which accelerates the conduction of lithium ions.

Copper-Catalyzed Cyclization/Dimerization of Tryptamines with O/Air as the Sole Oxidant: Direct Access to Complex Bispyrrolidino[2,3-]indoline.

The first transition metal catalytic one-step synthesis of the 3a, 3a'-bispyrrolidino [2,3-] indoline scaffold via tandem cyclization/dimerization of tryptamines has been realized with the environmentally friendly O/air as the sole oxidant. Different from the traditional direct oxidation of indole "N-H" group by excess amount of metal salts, a copper-catalyzed oxidative cyclization reaction is developed for the formation of the radical pyrrolidinoindoline intermediate in the current strategy. The robustness and practicality of this methodology is demonstrated by the step-economic, divergent total synthesis of natural products (±)-folicanthine and -folicanthine.

Assembly of Lanthanide-Containing Tungstotellurates(VI): Syntheses, Structures, and Catalytic Properties.

Lanthanide (Ln)-containing polyoxometalates (POMs) have attracted particular attention owing to their structural diversity and potential applications in luminescence, magnetism, and catalysis. Herein three types of Ln-containing tungstotellurates(VI) (Ln = Dy, Ho, Er, Tm, Yb, and Lu), dimeric (DMAH) [H {Ln(HO)[TeWO]}]mHO (abbreviated as {LnTeW}; DMAH = dimethylammonium), mono-substituted (DMAH)Na{HLn(HO)[TeWO]}mHO (abbreviated as {LnTeW}), and three-dimensional (3D) inorganic frameworks (DMAH) {H Ln(HO)[TeWO]}mHO (abbreviated as {LnTeW}), have been synthesized by using simple metal salts and characterized by single-crystal X-ray diffraction and other routine techniques. Interestingly, the assembly of these POMs is pH dependent.

Clinical and radiologic correlates of neurotoxicity after axicabtagene ciloleucel in large B-cell lymphoma.

Neurotoxicity or immune effector cell-associated neurotoxicity syndrome (ICANS) is the second most common acute toxicity after chimeric antigen receptor (CAR) T-cell therapy. However, there are limited data on the clinical and radiologic correlates of ICANS. We conducted a cohort analysis of 100 consecutive patients with relapsed or refractory large B-cell lymphoma (LBCL) treated with standard of care axicabtagene ciloleucel (axi-cel).

Near-Infrared Emission Induced by Shortened Pt-Pt Contact: Diplatinum(II) Complexes with Pyridyl Pyrimidinato Cyclometalates.

Four diplatinum(II) complexes with the formula [Pt(pypm)(μ-F)] (, -) bearing both a pyridine-pyrimidinate chelate and formamidinate bridge, where (pypm)H and FH stand for 5-(pyridin-2-yl)-2-(trifluoromethyl)pyrimidine and functional formamidines with various substituents of Pr ( = 1), Ph ( = 2), CHBu ( = 3), and CHCF ( = 4), were synthesized en route from a mononuclear intermediate represented by [Pt(pypm)Cl(FH)] (). Single-crystal X-ray diffraction studies confirmed the structure of and comprised of an individual "Pt(pypm)" unit and two "Pt(pypm)" units with a Pt···Pt distance of 2.8845(2) Å, respectively.

Recoverable amphiphilic polyoxoniobates catalyzing oxidative and hydrolytic decontamination of chemical warfare agent simulants in emulsion.

Amphiphilic polyoxoniobates (PONbs), [CHN(CH)]HNbO (for 1, n=14; for 2, n=16; and for 3, n=18), were successfully prepared by the electrostatic interaction of hexaniobate anions with quaternary ammoniums containing long alkyl chain, and thoroughly characterized by using various techniques including Fourier transform infrared (FT-IR), H nuclear magnetic resonance (H NMR), C nuclear magnetic resonance (C NMR), thermogravimetric analysis (TGA), and elemental analysis. All three PONbs were used in the emulsion systems to catalytically decontaminate chemical warfare agent simulants and the influences of quaternary ammonium cations, polyanions, and amount of catalyst on the catalytic efficiency have been evaluated. Under optimal conditions, catalyst 3 in emulsion can completely convert both a the nerve agent simulant, diethyl cyanophosphonate (DECP), in 2h by hydrolysis and a sulfur mustard simulant, 2-chloroethyl ethyl sulfide (CEES), in 20min by oxidation using nearly stoichiometric 3% aqueous HO.

Toward High-Level Theoretical Studies of Large Biodiesel Molecules: An ONIOM [QCISD(T)/CBS:DFT] Study of the Reactions between Unsaturated Methyl Esters (C HCOOCH) and Hydrogen Radical.

A two-layer ONIOM[QCISD(T)/CBS:DFT] method was proposed for the high-level single-point energy calculations of large biodiesel molecules and was validated for the hydrogen abstraction reactions of unsaturated methyl esters that are important components of real biodiesel. The reactions under investigation include all the reactions on the potential energy surface of C HCOOCH ( n = 2-5, 17) + H, including the hydrogen abstraction, the hydrogen addition, the isomerization (intramolecular hydrogen shift), and the β-scission reactions. By virtue of the introduced concept of chemically active center, a unified specification of chemically active portion for the ONIOM (ONIOM = our own n-layered integrated molecular orbital and molecular mechanics) method was proposed to account for the additional influence of C═C double bond.

Black N/H-TiO Nanoplates with a Flower-Like Hierarchical Architecture for Photocatalytic Hydrogen Evolution.

A facile two-step strategy was used to prepare black of hydrogenated/nitrogen-doped TiO nanoplates (NHTA) with a flower-like hierarchical architecture. In situ nitriding and self-assembly was realized by hydrothermal synthesis using tripolycyanamide as a N source and as a structure-directing agent. After thorough characterization, it was found that the hydrogenation treatment did not damage the flower-like architecture but distorted the anatase crystal structure and significantly changed the band structure of NHTA owing to the increased concentration of oxygen vacancies, hydroxyl groups, and Ti cations.

A new insight into the chemistry of iridium(III) complexes bearing phenyl phenylphosphonite cyclometalate and chelating pyridyl triazolate: the excited-state proton transfer tautomerism via an inter-ligand PO-H···N hydrogen bond.

Treatment of [IrCl3(tht)3], where tht = tetrahydrothiophene, with two equiv. of phenyl diphenylphosphinite (pdpitH) gave [Ir(pdpitH)(pdpit)(tht)Cl2] (1), which on further reaction with 3-t-butyl-5-(2-pyridyl)-1,2,4-triazole (bptzH) and NaOAc using a one-pot reaction afforded [Ir(pdpit)2(bptz)] (2). In sharp contrast, the reaction of [IrCl3(tht)3], pdpitH, and bptzH in the presence of a stronger base, Na2CO3, afforded a phenyl phenylphosphonite (pppo)-containing Ir(III) complex [Ir(pdpit)(pppo)(bptz)] (3) that reveals a strong PO-H-N inter-ligand hydrogen bond (H-bond), as evidenced by the single crystal X-ray structural analysis.

Copper-catalyzed decarboxylative C3-acylation of free (N-H) indoles with α-oxocarboxylic acids.

An efficient Cu-catalyzed decarboxylative C3-acylation of free (N-H) indoles using α-oxocarboxylic acids as acylating agents has been developed. This method was compatible with a variety of functional groups and provided an attractive alternative access to 3-acylindoles in moderate to high yields.

Phosphorescent Ir(III) complexes with both cyclometalate chromophores and phosphine-silanolate ancillary: concurrent conversion of organosilane to silanolate.

Ir(III) metal complexes with general formula [(C^N)2Ir(P^SiO)], where (C^N)H is 2-phenylisoquinoline (1), 2-phenylpyridine (2) or 2-(2,4-difluorophenyl)pyridine (3), and (P^SiO)H is an organosilanolate ancillary chelate with either diphenylsilyl (a) or dimethylsilyl (b) substituent, were synthesized, among which the structure of 3a was also confirmed using single-crystal X-ray diffraction analyses. These complexes exhibit bright phosphorescence in the region of 489-632 nm in solution at room temperature, showing the first successful example of using organosilanolate as an ancillary chelate. For application, organic light emitting diodes (OLEDs) using phosphors 3a and 3b doped in N,N'-dicarbazolyl-3,5-benzene (mCP) exhibited a maximum brightness of 50,800 cd m(-2) at 800 mA cm(-2) (12 V) with η(ext) of 10.

Homoleptic tris(pyridyl pyrazolate) Ir(III) complexes: en route to highly efficient phosphorescent OLEDs.

Treatment of the metal reagent IrCl(3)nH(2)O with two equivalents of 2-pyridyl pyrazole (N;N)H (3-tert-butyl-5-(2-pyridyl) pyrazole, (bppz)H and 3-trifluoromethyl-5-(2-pyridyl) pyrazole, (fppz)H), afforded the isomeric Ir(III) metal complexes with a general formula cis-[Ir(bppz)(2)Cl(2)]H (2 a), trans-[Ir(bppz)(2)Cl(2)]H (3 a), cis-[Ir(fppz)(2)Cl(2)]H (2 b), and trans-[Ir(fppz)(2)Cl(2)]H (3 b). Single-crystal X-ray diffraction studies on 2 b and 3 a revealed the coexistence of two pyrazolate chelates and two terminal chloride ligands on the coordination sphere. Subsequent reactivity studies confirmed their intermediacy to the preparation of homoleptic mer-[Ir(bppz)(3)] (1 a) and mer-[Ir(fppz)(3)] (1 b) that showed dual intraligand and ligand-to-ligand charge-transfer phosphorescence at room temperature.

Transition-metal phosphors with cyclometalating ligands: fundamentals and applications.

One goal of this critical review is to provide advanced methodologies for systematic preparation of transition-metal based phosphors that show latent applications in the field of organic light emitting diodes (OLEDs). We are therefore reviewing various types of cyclometalating chelates for which the favorable metal-chelate bonding interaction, on the one hand, makes the resulting phosphorescent complexes highly emissive in both fluid and solid states at room temperature. On the other hand, fine adjustment of ligand-centered pi-pi* electronic transitions allows tuning of emission wavelength across the whole visible spectrum.

New series of ruthenium(II) and osmium(II) complexes showing solid-state phosphorescence in far-visible and near-infrared.

A new Ru(II) complex, [Ru(fpbpymH)(2)]Cl(2) (1), in which fpbpymH = [5-(trifluoromethyl)pyrazol-3-yl](2,2'-bipyrid-6-yl)methane, was prepared by the treatment of [Ru(DMSO)(4)Cl(2)] with 2 equiv of the terdentate chelate fpbpymH in refluxing ethanol. A single-crystal X-ray diffraction study of 1 revealed a distorted octahedral Ru(II) framework, showing strong N-H..