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Organic materials have attracted much attention for their utility as lithium-battery electrodes because their tunable structures can be sustainably prepared from abundant precursors in an environmentally friendly manner. Most research into organic electrodes has focused on the material level instead of evaluating performance in practical batteries. This Review addresses this by first providing an overview of the history and redox of organic electrode materials and then evaluating the prospects and remaining challenges of organic electrode materials for practical lithium batteries. Our evaluations are made according to energy density, power density, cycle life, gravimetric density, electronic conductivity and other relevant parameters, such as energy efficiency, cost and resource availability. We posit that research in this field must focus more on the intrinsic electronic conductivity and density of organic electrode materials, after which a comprehensive optimization of full batteries should be performed under practically relevant conditions. We hope to stimulate high-quality applied research that might see the future commercialization of organic electrode materials. Organic materials can serve as sustainable electrodes in lithium batteries. This Review describes the desirable characteristics of organic electrodes and the corresponding batteries and how we should evaluate them in terms of performance, cost and sustainability.

It is unknown whether the human immune system frequently mounts a T cell response against mutations expressed by common epithelial cancers. Using a next-generation sequencing approach combined with high-throughput immunologic screening, we demonstrated that tumor-infiltrating lymphocytes (TILs) from 9 out of 10 patients with metastatic gastrointestinal cancers contained CD4⁺ and/or CD8⁺ T cells that recognized one to three neo-epitopes derived from somatic mutations expressed by the patient's own tumor. There were no immunogenic epitopes shared between these patients. However, we identified in one patient a human leukocyte antigen–C*08:02–restricted T cell receptor from CD8⁺ TILs that targeted the KRASG12D hotspot driver mutation found in many human cancers. Thus, a high frequency of patients with common gastrointestinal cancers harbor immunogenic mutations that can potentially be exploited for the development of highly personalized immunotherapies.

Immunotherapy using either checkpoint blockade or the adoptive transfer of antitumor lymphocytes has shown effectiveness in treating cancers with high levels of somatic mutations—such as melanoma, smoking-induced lung cancers and bladder cancer—with little effect in other common epithelial cancers that have lower mutation rates, such as those arising in the gastrointestinal tract, breast and ovary 1 – 7 . Adoptive transfer of autologous lymphocytes that specifically target proteins encoded by somatically mutated genes has mediated substantial objective clinical regressions in patients with metastatic bile duct, colon and cervical cancers 8 – 11 . We present a patient with chemorefractory hormone receptor (HR)-positive metastatic breast cancer who was treated with tumor-infiltrating lymphocytes (TILs) reactive against mutant versions of four proteins—SLC3A2, KIAA0368, CADPS2 and CTSB. Adoptive transfer of these mutant-protein-specific TILs in conjunction with interleukin (IL)-2 and checkpoint blockade mediated the complete durable regression of metastatic breast cancer, which is now ongoing for >22 months, and it represents a new immunotherapy approach for the treatment of these patients. Adoptive T cell therapy induced complete and durable remission in a patient with refractory metastatic breast cancer, providing proof of principle for this approach in breast cancer therapy.

In this paper, we tentatively assign the Pc(4312) to be a D¯Σc molecular state with quantum number JP=12-, and calculate its magnetic moment using the QCD sum rule method in external weak electromagnetic field. Starting with the two-point correlation function in external electromagnetic field and expanding it in power of the electromagnetic interaction Hamiltonian, we extract the magnetic moment from the linear response to the external electromagnetic field. The numerical value of the magnetic moment of Pc(4312) is μPc=1.75-0.11+0.15.

Aim Myocardial infarction (MI) is a severe disease with increased mortality and disability rates, posing heavy economic burden for society. Exosomes were uncovered to mediate intercellular communication after MI. This study aims to explore the effect and mechanism of lncRNA KLF3-AS1 in exosomes secreted by human mesenchymal stem cells (hMSCs) on pyroptosis of cardiomyocytes and MI. Methods Exosomes from hMSCs were isolated and identified. Exosomes from hMSCs with transfection of KLF3-AS1 for overexpression were injected into MI rat model or incubated with hypoxia cardiomyocytes. Effect of KLF3-AS1 on MI area, cell viability, apoptosis, and pyroptosis was determined. The relationship among miR-138-5p, KLF3-AS1, and Sirt1 was verified by dual-luciferase reporter assay. Normal cardiomyocytes were transfected with miR-138-5p inhibitor or sh-Sirt1 to clarify whether alteration of miR-138-5p or sh-Sirt1 can regulate the effect of KLF3-AS1 on cardiomyocytes. Results Exosomes from hMSCs were successfully extracted. Transfection of KLF3-AS1 exosome in rats and incubation with KLF3-AS1 exosome in hypoxia cardiomyocytes both verified that overexpression of KLF3-AS1 in exosomes leads to reduced MI area, decreased cell apoptosis and pyroptosis, and attenuated MI progression. KLF3-AS1 can sponge miR-138-5p to regulate Sirt1 expression. miR-138-5p inhibitor transfection and KLF3-AS1 exosome incubation contribute to attenuated pyroptosis and MI both in vivo and in vitro, while transfection of sh-Sirt1 could reverse the protective effect of exosomal KLF3-AS1 on hypoxia cardiomyocytes. Conclusion LncRNA KLF3-AS1 in exosomes secreted from hMSCs by acting as a ceRNA to sponge miR-138-5p can regulate Sirt1 so as to inhibit cell pyroptosis and attenuate MI progression.

Given that cancer mortality is usually a result of late diagnosis, efforts in the field of early detection are paramount to reducing cancer-related deaths and improving patient outcomes. Increasing evidence indicates that metastasis is an early event in patients with aggressive cancers, often occurring even before primary lesions are clinically detectable. Metastases are usually formed from cancer cells that spread to distant non-malignant tissues via the blood circulation, termed circulating tumour cells (CTCs). CTCs have been detected in patients with early stage cancers and, owing to their association with metastasis, might indicate the presence of aggressive disease, thus providing a possible means to expedite diagnosis and treatment initiation for such patients while avoiding overdiagnosis and overtreatment of those with slow-growing, indolent tumours. The utility of CTCs as an early diagnostic tool has been investigated, although further improvements in the efficiency of CTC detection are required. In this Perspective, we discuss the clinical significance of early haematogenous dissemination of cancer cells, the potential of CTCs to facilitate early detection of clinically relevant cancers, and the technological advances that might improve CTC capture and, thus, diagnostic performance in this setting.The authors of this Perspective propose that, with further improvement in detection efficiency, circulating tumour cells (CTCs), which are released early during cancer development, have the potential to be used for the early detection of clinically relevant, aggressive cancers. Thus, use of CTCs as diagnostic biomarkers might improve outcomes by enabling the identification of cancers at a stage at which they are more amenable to treatment while avoiding overtreatment of patients with indolent tumours.

Detecting small targets in UAV remote sensing images is challenging for traditional lightweight methods due to difficulty in feature extraction and high background interference. We propose LPS-YOLO, which improves small target feature extraction while reducing computational complexity by replacing the Conv backbone with SPDConv to retain fine-grained features. LPS-YOLO introduces the SKAPP module for better feature fusion and incorporates the E-BiFPN and OFTP structures to efficiently preserve and transfer backbone information. Evaluation of the VisDrone2019 dataset shows a 17.3% increase in mean Average Precision (mAP) and a 42.5% reduction in parameters compared to the baseline. Additional experiments on the DOTAv2 dataset demonstrate the model’s robustness, with a 14.5% improvement in F1 score and a 14.9% increase in mAP over YOLOv8-n. LPS-YOLO offers an effective solution for multi-target detection in UAVs.

The Zhunuo porphyry copper deposit in the Gangdese belt of southern Tibet contains 2.37 Mt at 0.57% Cu. In this deposit, Eocene rhyolite (51.6 ± 1.0 Ma) and quartz porphyry (49.1 ± 0.6 Ma) were intruded by monzogranite (14.7 ± 0.3 Ma) and monzogranite porphyry (14.5 ± 0.2 Ma) which commonly host mafic microgranular enclaves (14.9 ± 0.3 Ma). Late-mineralization diorite porphyry (14.2 ± 0.2 Ma) and post-mineralization lamprophyre dikes (12.2 ± 0.1 Ma) and granite porphyry (12.0 ± 0.2 Ma) crosscut the Miocene intrusions. Two quartz–molybdenittie veins yielded molybdenite Re-Os model ages of 14.8 ± 0.1 Ma and 14.4 ± 0.1 Ma, and another two quartz–muscovite–llite–pyrite–molybdenite veins yielded molybdenite Re-Os model ages of 14.2 ± 0.1 Ma and 13.5 ± 0.1 Ma. Zhunuo is characterized by early potassic alteration and associated quartz A veins centered on the monzogranite porphyry and adjacent monzogranite, distal propylitic alteration in the rhyolite, and late-stage phyllic alteration and associated quartz B veins, followed by D veins that affected quartz porphyry and potassic-altered rocks. Copper ores are mainly distributed in the potassic alteration zone that was overprinted by phyllic alteration. Copper mineralization likely occurred during potassic alteration stage and was locally remobilized and redeposited during phyllic alteration stage, or occurred during phyllic alteration stage. The post-mineralization granite porphyry has lower whole-rock Sr/Y (< 20) and εNd(t) (− 9.3 to − 9.0) and higher zircon U/Yb (4 to 27) than the Miocene intrusions (Sr/Y > 40; εNd(t) = − 6.9 to − 6.1; U/Yb = 1 to 10). Limited input of juvenile melts could explain the low potential for copper mineralization in the post-mineralization granite porphyry at Zhunuo.

A woman with KRAS -mutated colon cancer had a response to T cells derived from her tumor that were specific for mutant KRAS. A lesion recurring 9 months later had lost expression of the class I major histocompatibility complex molecule recognized by the T cells. Adoptive cell therapy using ex vivo expanded tumor-infiltrating lymphocytes has led to durable complete regression of tumors in 20 to 25% of patients with metastatic melanoma. 1 , 2 This effect is probably mediated by T cells that specifically target mutant peptides encoded by de novo somatic mutations, which are known as neoepitopes. 3 – 8 Correlative evidence suggests that clinical responses in patients with cancer after the administration of immune checkpoint inhibitors may also be mediated by neoepitope-reactive T cells. 9 – 14 Direct evidence of the therapeutic utility of the targeting of neoepitopes was observed in a patient with metastatic cholangiocarcinoma who had tumor . . .

Summary The Orchidaceae is of economic and ecological importance and constitutes ˜10% of all seed plant species. Here, we report a genome physical map for Cymbidium sinense, a well‐known species belonging to genus Cymbidium that has thousands of natural variation varieties of flower organs, flower and leaf colours and also referred as the King of Fragrance, which make it arose into a unique cultural symbol in China. The high‐quality chromosome‐scale genome assembly was 3.52 Gb in size, 29 638 protein‐coding genes were predicted, and evidence for whole‐genome duplication shared with other orchids was provided. Marked amplification of cytochrome‐ and photosystem‐related genes was observed, which was consistent with the shade tolerance and dark green leaves of C. sinense. Extensive duplication of MADS‐box genes, and the resulting subfunctional and expressional differentiation, was associated with regulation of species‐specific flower traits, including wild‐type and mutant‐type floral patterning, seasonal flowering and ecological adaption. CsSEP4 was originally found to positively regulate gynostemium development. The CsSVP genes and their interaction proteins CsAP1 and CsSOC1 were significantly expanded and involved in the regulation of low‐temperature‐dependent flowering. Important genetic clues to the colourful leaf traits, purple‐black flowers and volatile trait in C. sinense were also found. The results provide new insights into the molecular mechanisms of important phenotypic traits of Cymbidium and its evolution and serve as a powerful platform for future evolutionary studies and molecular breeding of orchids.