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Optical wave propagation in magneto-optic waveguides with generalized anti-cubic model. 广义反三次模型磁光波导中的光波传播。
IF 2.9 4区 综合性期刊 Q2 MULTIDISCIPLINARY SCIENCES Pub Date : 2026-01-01 Epub Date: 2026-01-14 DOI: 10.1177/00368504251414606
Muhammad Zafarullah Baber, Muhammad Waqas Yasin, Nauman Ahmed, Khadeeja Arif, Baboucarr Ceesay

This study investigates optical solitons in magneto-optic waveguides while preserving the generalized anti-cubic structure of nonlinear self-phase modulation. A novel ϕ6-model expansion technique is proposed, and its application in magneto-optic waveguides is explored. The ϕ6 approach provides an accurate and efficient method to solve wave propagation problems in magneto-optic media, enabling improved modeling of light behavior by incorporating the combined effects of electric and magnetic fields within a unified framework. To address the challenges arising from the nonlinear magneto-optic effects on waveguide characteristics, the method yields precise dispersion relations, field distributions, and transmission properties. This technique facilitates the design of magneto-optic waveguides with tailored characteristics for next-generation photonic systems. By offering a reliable and accurate modeling framework, the ϕ6 approach contributes to the development of more precise and efficient magneto-optic devices, advancing photonic integration, communication, and sensing technologies.

本文研究了磁光波导中保留非线性自相位调制广义反立方结构的光孤子。提出了一种新的ϕ6模型展开技术,并对其在磁光波导中的应用进行了探讨。在磁光介质中,通过将电场和磁场的综合效应纳入一个统一的框架,从而改进了光行为的建模,从而提供了一种精确而有效的方法来解决波的传播问题。为了解决非线性磁光效应对波导特性带来的挑战,该方法产生了精确的色散关系、场分布和传输特性。该技术有助于设计具有定制特性的磁光波导,用于下一代光子系统。通过提供可靠和准确的建模框架,该方法有助于开发更精确和高效的磁光器件,推进光子集成,通信和传感技术。
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引用次数: 0
The weight-adjusted-waist index is positively associated with metabolic dysfunction-associated fatty liver disease in US adults: A cross-sectional NHANES Study. 美国成人体重调整腰围指数与代谢功能障碍相关的脂肪肝疾病呈正相关:一项横断面NHANES研究
IF 2.9 4区 综合性期刊 Q2 MULTIDISCIPLINARY SCIENCES Pub Date : 2026-01-01 Epub Date: 2026-02-03 DOI: 10.1177/00368504261420942
Pingping Liu, Wei Zhao, Daochong Qiu, Yuping Li

ObjectivesMetabolic dysfunction-associated fatty liver disease (MAFLD) poses a major global health burden due to risks of cirrhosis and liver cancer; however, the relationship between MAFLD and weight-adjusted-waist index (WWI) remains unclear. Our study aims to clarify this relationship and identify potential clinical predictors for MAFLD.MethodsA population-based cross-sectional study was conducted using data from the National Health and Nutrition Examination Survey (NHANES) 1999-2010 and 2015-2018. Multivariable logistic regression and Restricted Cubic Splines (RCS) was employed to examine the nonlinear association between WWI and MAFLD. Following this, a subgroup analysis was performed to detect any variations and ensure the robustness of the findings.ResultsThe study included 17,930 participants aged ≥ 18 years, with a mean age of 45.54 years and 48.43% males. The sample was comprised of 44.36% Non-Hispanic White, 20.69% Mexican American, 19.55% Non-Hispanic Black, 8.00% Other Hispanic, and 7.41% Other/Multi-Racial individuals. Among them, 5850 individuals were diagnosed with MAFLD. The study found a statistically significant association between WWI and MAFLD (odds ratio (OR) = 4.35, 95% confidence interval [95% CI]: 4.08-4.63), which remained significant even after adjusting for all relevant factors (OR = 2.73, 95% CI: 2.48-3.01). The RCS analysis revealed a significant nonlinear relationship between WWI and MAFLD (p < 0.05). Subgroup analysis indicated that WWI remained positively correlated with MAFLD, but no significant interaction was observed (p-interaction > 0.05)ConclusionsWWI is a significant predictor of MAFLD, suggesting its potential as a simple, non-invasive screening tool for the occurrence of MAFLD.

代谢功能障碍相关脂肪性肝病(MAFLD)由于肝硬化和肝癌的风险而成为全球主要的健康负担;然而,MAFLD与体重调整腰围指数(WWI)之间的关系尚不清楚。我们的研究旨在澄清这种关系,并确定MAFLD的潜在临床预测因素。方法采用1999-2010年和2015-2018年国家健康与营养检查调查(NHANES)的数据进行基于人群的横断面研究。采用多变量逻辑回归和限制三次样条(RCS)分析了WWI与MAFLD之间的非线性关系。在此之后,进行亚组分析以检测任何变化并确保结果的稳健性。结果纳入17930名年龄≥18岁的参与者,平均年龄45.54岁,男性占48.43%。样本由44.36%的非西班牙裔白人、20.69%的墨西哥裔美国人、19.55%的非西班牙裔黑人、8.00%的其他西班牙裔和7.41%的其他/多种族个体组成。其中5850人被诊断为MAFLD。研究发现第一次世界大战与MAFLD之间存在统计学上显著的关联(优势比(OR) = 4.35, 95%可信区间[95% CI]: 4.08-4.63),即使在调整了所有相关因素后,这一关联仍然显著(OR = 2.73, 95% CI: 2.48-3.01)。RCS分析显示WWI与MAFLD之间存在显著的非线性关系(p - p-interaction > 0.05)。结论swwi是MAFLD的重要预测因子,提示其作为一种简单、无创的MAFLD筛查工具的潜力。
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引用次数: 0
Lingual metastasis from primary pulmonary adenoid cystic carcinoma: A rare case report. 原发性肺腺样囊性癌舌部转移一例。
IF 2.9 4区 综合性期刊 Q2 MULTIDISCIPLINARY SCIENCES Pub Date : 2026-01-01 Epub Date: 2026-02-03 DOI: 10.1177/00368504261418808
Yu Zhang, Jia-Qi Zhu, Wei Shang, Zong-Xuan He

Adenoid cystic carcinoma (AdCC) is a malignancy that most frequently originates in the salivary glands of the head and neck, though it may also rarely occur in other sites such as the trachea or breast. It is characterized by its slow-growing nature in the early stages, along with distinctive features of perineural invasion and a tendency for late metastasis, particularly to the lungs. Recurrence or metastasis can occur even years after the initial treatment. Currently, no standardized clinical protocol exists for long-term follow-up. The disease can recur or metastasize even years after initial treatment. At present, no uniform clinical protocol exists for long-term follow-up. To our knowledge, no documented cases of retrograde metastasis from primary pulmonary AdCC to the tongue have been reported. We describe the case of a male patient in his 40s with primary low-grade pulmonary AdCC who developed lingual metastasis after aggressive treatment. This case highlights an unusual metastatic pattern and underscores the need for vigilant, long-term monitoring of patients with AdCC.

腺样囊性癌(AdCC)是一种最常起源于头颈部唾液腺的恶性肿瘤,尽管它也可能很少发生在气管或乳房等其他部位。它的特点是早期生长缓慢,具有明显的神经周围侵袭和晚期转移的倾向,特别是肺。复发或转移可能在最初治疗数年后发生。目前,尚无标准化的长期随访临床方案。这种疾病可能在最初治疗数年后复发或转移。目前尚无统一的长期随访临床方案。据我们所知,没有文献报道原发性肺AdCC向舌部逆行转移的病例。我们描述了一个40多岁的男性患者,原发低级别肺AdCC,在积极治疗后发生舌转移。该病例强调了一种不寻常的转移模式,并强调了对AdCC患者进行警惕和长期监测的必要性。
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引用次数: 0
Optimizing radiotherapy for early-stage breast cancer: A comparative SEER-based analysis of neoadjuvant, intraoperative, and postoperative approaches. 优化早期乳腺癌放疗:基于seer的新辅助、术中和术后入路比较分析
IF 2.9 4区 综合性期刊 Q2 MULTIDISCIPLINARY SCIENCES Pub Date : 2026-01-01 Epub Date: 2026-01-30 DOI: 10.1177/00368504261420988
Lingrui Li, Xiangyi Kong, Zhuang Xiong, Xiangyu Wang, Wenxiang Zhang, Yi Fang, Zhongzhao Wang, Jing Wang

ObjectiveTo compare long-term survival in early-stage breast cancer patients treated with different radiation therapy modalities.MethodsData was retrospectively derived from SEER database. We compared overall survival (OS), breast cancer specific survival (BCSS) and second primary malignancies (SPM) in early-stage breast cancer patients treated with postoperative radiotherapy (PORT) versus those treated neoadjuvant radiotherapy (NART) and intraoperative radiotherapy (IORT) after propensity score matching by 1:1.ResultsA total of 457,166 patients were included in this study. After matching, the 20-year OS of 1441 patients in NART cohort was lower than that in PORT cohort (p < 0.01), particularly in hormone receptor positive patients (p < 0.01). NART were dependent prognostic factors for 20-year OS [Hazard Ratio (HR):1.21, 95%CI: 1.06-1.38, p < 0.01). No significant difference in BCSS was observed between NART and PORT treatments. Additionally, patients undergoing NART had a lower risk of all SPM (p = 0.01) and second solid cancers (p = 0.02) but a comparable risk of second hematological malignancies (p = 0.55) than patients administered PORT. HR-positive was a risk factor for SPM. No OS, BCSS or SPM risk difference were significantly observed in the 2096 pairs of IORT and PORT groups.ConclusionCompared to PORT, NART and IORT don't offer survival advantages for early-stage breast cancer patients. Altering the sequence of radiotherapy requires careful evaluation.

目的比较不同放射治疗方式对早期乳腺癌患者的长期生存率。方法回顾性数据来源于SEER数据库。我们比较了接受术后放疗(PORT)的早期乳腺癌患者与接受新辅助放疗(NART)和术中放疗(IORT)的早期乳腺癌患者的总生存率(OS)、乳腺癌特异性生存率(BCSS)和第二原发恶性肿瘤(SPM),倾向评分匹配为1:1。结果共纳入457166例患者。配对后,1441例NART队列患者的20年OS低于PORT队列患者(p
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引用次数: 0
Biochemical indicators, physical activity, and functional performance in elderly CKD patients: A cross-sectional study. 老年CKD患者的生化指标、体力活动和功能表现:一项横断面研究
IF 2.9 4区 综合性期刊 Q2 MULTIDISCIPLINARY SCIENCES Pub Date : 2026-01-01 Epub Date: 2026-01-29 DOI: 10.1177/00368504261417773
Quan Wen, Qing Ye, Yiming Sun, Xinru Liu, Jie Yang, Hui Men, Yuee Tan, Suyang Yuan, Yu Dai

ObjectiveThis study aimed to investigate the clinical characteristics of elderly chronic kidney disease (CKD) patients; and the correlation among their biochemical indicators, physical activity, and functional parameters. The findings of this study will hopefully a scientific basis for better understanding the causes and developing the best management methods for CKD in this population.MethodsIn total, 280 elderly patients with CKD participated in this cross-sectional study. All patients underwent a multidimensional assessment of clinical data, physical activity, and functional performance. Patients were stratified by disease severity into two groups: CKD stages 1-3 and stages 4-5. Additionally, they were categorized as sedentary or nonsedentary based on metabolic equivalent of task (MET) levels. Inter-group differences and correlations among the variables were subsequently analyzed.ResultsResearch findings indicated that although male patients predominated in the overall cohort, female patients were more prevalent among those with advanced CKD (stages 4-5) and those reporting a sedentary lifestyle, and these subgroups also demonstrated a higher likelihood of hypertension and anemia. Compared to patients with CKD stages 1-3, those in stages 4-5 had significantly lower estimated glomerular filtration rate (eGFR), hemoglobin, albumin, and MET values (P < .05), along with higher serum creatinine and Barthel Index of Activities of Daily Living (BADL) values (P < .05). Similarly, when compared to nonsedentary patients, those with a sedentary lifestyle exhibited lower eGFR, hemoglobin, and MET levels (P < .05), alongside elevated procalcitonin (PCT) and BADL values (P < .05). Correlation analyses further revealed that renal function was significantly associated with both BADL and MET values in the studied CKD population (P < .05). Our correlation analysis also revealed that renal function in elderly advanced CKD patients is closely associated with levels of PCT and Hb (P < .05). Moreover, among sedentary elderly CKD patients, renal function was correlated not only with PCT and Hb (P < .05), but also with albumin and physical activity levels MET (P < .05).ConclusionsOur study identified a predominance of female patients in advanced CKD stages and among those leading sedentary lifestyles. Furthermore, our findings suggest that renal function may be associated with physical activity and functional performance, with this relationship appearing most pronounced in sedentary individuals. The results also point to a potential interrelationship between renal function, inflammation, and nutritional status in advanced CKD.

目的探讨老年慢性肾病(CKD)患者的临床特点;以及他们的生化指标、身体活动和功能参数之间的相关性。本研究的发现有望为更好地了解该人群CKD的原因和制定最佳管理方法提供科学依据。方法共280例老年CKD患者参与了本横断面研究。所有患者都接受了临床数据、身体活动和功能表现的多维评估。根据病情严重程度将患者分为两组:CKD 1-3期和4-5期。此外,根据任务代谢当量(MET)水平,他们被分为久坐或不久坐。随后分析了组间差异和变量之间的相关性。研究结果表明,尽管男性患者在整个队列中占主导地位,但女性患者在晚期CKD(4-5期)和报告久坐生活方式的人群中更为普遍,并且这些亚组也显示出更高的高血压和贫血的可能性。与CKD 1-3期患者相比,4-5期患者的肾小球滤过率(eGFR)、血红蛋白、白蛋白和MET值的估计值显著降低(P < 0.05),血清肌酐和Barthel日常生活活动指数(BADL)值较高(P < 0.05)。同样,与不久坐的患者相比,久坐生活方式的患者eGFR、血红蛋白和MET水平较低(P < 0.05),同时降钙素原(PCT)和BADL值升高(P < 0.05)。相关分析进一步显示,在CKD研究人群中,肾功能与BADL和MET值均显著相关(P < 0.05)。我们的相关分析还显示,老年晚期CKD患者的肾功能与PCT和Hb水平密切相关(P < 0.05)。此外,在久坐的老年CKD患者中,肾功能不仅与PCT和Hb相关(P < 0.05),还与白蛋白和身体活动水平MET相关(P < 0.05)。我们的研究发现,女性患者在CKD晚期和久坐生活方式中占主导地位。此外,我们的研究结果表明,肾功能可能与身体活动和功能表现有关,这种关系在久坐的个体中表现得最为明显。研究结果还指出,肾功能、炎症和晚期CKD的营养状况之间存在潜在的相互关系。
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引用次数: 0
AI-driven patient-centered care: A digital transformation framework for gynecologic cancer genetic counseling. 人工智能驱动的以患者为中心的护理:妇科癌症遗传咨询的数字化转型框架。
IF 2.9 4区 综合性期刊 Q2 MULTIDISCIPLINARY SCIENCES Pub Date : 2026-01-01 Epub Date: 2026-01-19 DOI: 10.1177/00368504251412703
Ruiye Yang, Xiaoran Zheng, Yaoqi Deng, Mengqi Deng, Junyi Jiang, Jinwei Miao

ObjectivesThis study evaluates artificial intelligence (AI) reasoning capabilities in gynecologic cancer genetic counseling, comparing the performance of ChatGPT and DeepSeek models to guide patient-centered AI implementation in clinical genetics.MethodsUsing 40 National Comprehensive Cancer Network-aligned counseling scenarios, we conducted blinded dual-oncologist evaluations of two large language models. Methodological rigor included model anonymization, a pre-calibrated scoring framework, and validated metrics (Global Quality Scale and Patient Education Materials Assessment Tool) assessing informational coherence, understandability, and actionability.ResultsDeepSeek demonstrated superior informational breadth (mean character difference: -609.0, p < .0001) and visual communication (diagram integration, p < .01), with 49-fold greater probability in recommending clear and actionable actions (p < .01, OR = 49.0). ChatGPT excelled in concise summarization (22% faster response generation, p = .013).ConclusionStrategic AI model selection-leveraging DeepSeek's visually-rich, structured educational approach for complex information, and ChatGPT's concise, rapid summarization for efficient communication-enhances patient-centered genetic education when combined with clinician oversight. This framework supports healthcare's digital transformation by optimizing human-AI collaboration in hereditary cancer care.

目的评价人工智能(AI)在妇科癌症遗传咨询中的推理能力,比较ChatGPT和DeepSeek模型的性能,指导临床遗传学以患者为中心的AI实施。方法使用40个与国家综合癌症网络一致的咨询场景,我们对两种大型语言模型进行了双肿瘤学家盲法评估。方法的严谨性包括模型匿名化、预先校准的评分框架和经过验证的指标(全球质量量表和患者教育材料评估工具),评估信息的一致性、可理解性和可操作性。结果deepseek显示出优越的信息广度(平均字符差:-609.0,p p p p = 0.013)。策略性的人工智能模型选择——利用DeepSeek丰富的视觉、结构化的复杂信息教育方法,以及ChatGPT简洁、快速的高效沟通总结——结合临床医生的监督,增强以患者为中心的基因教育。该框架通过优化人类与人工智能在遗传性癌症治疗方面的合作,支持医疗保健的数字化转型。
{"title":"AI-driven patient-centered care: A digital transformation framework for gynecologic cancer genetic counseling.","authors":"Ruiye Yang, Xiaoran Zheng, Yaoqi Deng, Mengqi Deng, Junyi Jiang, Jinwei Miao","doi":"10.1177/00368504251412703","DOIUrl":"10.1177/00368504251412703","url":null,"abstract":"<p><p>ObjectivesThis study evaluates artificial intelligence (AI) reasoning capabilities in gynecologic cancer genetic counseling, comparing the performance of ChatGPT and DeepSeek models to guide patient-centered AI implementation in clinical genetics.MethodsUsing 40 National Comprehensive Cancer Network-aligned counseling scenarios, we conducted blinded dual-oncologist evaluations of two large language models. Methodological rigor included model anonymization, a pre-calibrated scoring framework, and validated metrics (Global Quality Scale and Patient Education Materials Assessment Tool) assessing informational coherence, understandability, and actionability.ResultsDeepSeek demonstrated superior informational breadth (mean character difference: -609.0, <i>p</i> < .0001) and visual communication (diagram integration, <i>p</i> < .01), with 49-fold greater probability in recommending clear and actionable actions (<i>p</i> < .01, OR = 49.0). ChatGPT excelled in concise summarization (22% faster response generation, <i>p</i> = .013).ConclusionStrategic AI model selection-leveraging DeepSeek's visually-rich, structured educational approach for complex information, and ChatGPT's concise, rapid summarization for efficient communication-enhances patient-centered genetic education when combined with clinician oversight. This framework supports healthcare's digital transformation by optimizing human-AI collaboration in hereditary cancer care.</p>","PeriodicalId":56061,"journal":{"name":"Science Progress","volume":"109 1","pages":"368504251412703"},"PeriodicalIF":2.9,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12816523/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145999821","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A radiomics nomogram based on ultrasound for predicting ablation zone disappearance after microwave ablation in patients with papillary thyroid microcarcinoma: A retrospective study. 基于超声的放射组学图预测甲状腺乳头状微癌微波消融后消融区消失的回顾性研究。
IF 2.9 4区 综合性期刊 Q2 MULTIDISCIPLINARY SCIENCES Pub Date : 2026-01-01 Epub Date: 2026-01-20 DOI: 10.1177/00368504261417129
Quan Wen, Zhixiang Wang, Yujiang Liu, Ying Feng, Lili Zhang, Yuan Zu, Linxue Qian

ObjectiveTo establish a predictive model based on ultrasound (US) radiomics to determine whether the ablation zone of papillary thyroid microcarcinoma (PTMC) disappears within 24 months after microwave ablation (MWA).Study designRetrospective study.MethodsThis study enrolled 201 PTMC patients who underwent MWA in Affiliated Beijing Friendship Hospital of Capital Medical University between January 2013 and September 2020. All patients were followed up at 1 h, 1 month, 3 months, 6 months, 12 months, and 24 months after MWA. Radiomics features were extracted from the preoperative US images, and a Rad-score was constructed. Univariate and multivariate logistic regression analyses were used to screen out the independent clinical factors associated with the disappearance of the ablation zone after MWA, and a radiomics nomogram was established to predict whether the ablation zone of PTMC disappeared within 24 months after MWA. The performance of the model was validated in the testing cohort.Results75.6% of patients achieved the ablation zone disappeared within 24 months after MWA. The disappearance rate was significantly associated with MWA energy and baseline lesion volume (p < 0.05). The US radiomics nomogram integrated Rad-score, MWA energy, and baseline lesion volume. In the testing cohort, the area under the curve of this nomogram outperformed that of the clinical model and the radiomics model (0.772 vs 0.714 and 0.679, respectively).ConclusionsThe nomogram based on US radiomics can reliably identify whether lesions of PTMC will disappear within 24 months after MWA. The nomogram is useful for screening optimal candidates for MWA and may assist clinicians and patients in choosing the best treatment option between MWA and surgery.

目的建立基于超声(US)放射组学的预测模型,预测微波消融(MWA)后24个月内甲状腺乳头状微癌(PTMC)消融区是否消失。研究设计回顾性研究。方法本研究纳入2013年1月至2020年9月在首都医科大学附属北京友谊医院行MWA治疗的201例PTMC患者。随访时间分别为MWA术后1小时、1个月、3个月、6个月、12个月、24个月。从术前US图像中提取放射组学特征,并构建rad评分。采用单因素和多因素logistic回归分析筛选与MWA后消融区消失相关的独立临床因素,建立放射组学图预测MWA后24个月内PTMC消融区是否消失。结果75.6%的患者在MWA术后24个月内消融区消失。消失率与MWA能量和基线病变体积显著相关(p
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引用次数: 0
Comparison of the differentially enriched mutations/pathways between stage II and stage IV dMMR/MSI-H colorectal cancer. II期和IV期dMMR/MSI-H结直肠癌差异富集突变/通路的比较
IF 2.9 4区 综合性期刊 Q2 MULTIDISCIPLINARY SCIENCES Pub Date : 2026-01-01 Epub Date: 2026-01-08 DOI: 10.1177/00368504251412580
Chun Han, Sisi Ye, Juan Li, Qian Qiao, Li Bai, Tingting Zhang

ObjectiveColorectal cancer (CRC) patients with high microsatellite instability (MSI-H) and mismatch repair deficiency (dMMR) had heterogeneous pathology and distinct prognoses. This study aimed to examine the difference in the gene expression profile of dMMR/MSI-H CRC patients with different disease stages and explore the different molecular mechanisms of disease progression.MethodsA total of 47 patients with dMMR/MSI-H CRC were enrolled and retrospectively studied, including 27 stage II and 20 stage IV patients. Each patient had paired tumor tissue and white blood cell samples, which were analyzed by next-generation sequencing (NGS) of 416 cancer-relevant genes. Pathway enrichment analysis was then performed to analyze the disease stage-specific signaling pathways.ResultsA total of 2878 mutation sites, spanning 378 mutated genes, were detected from the 47 dMMR/MSI-H CRC patients. The mutation frequencies of SMARCA4, EPHA3, MTHFR, RAD50, and PDGFRB were significantly higher in stage II patients than in stage IV patients (p < 0.05), whereas the stage II patients had significantly lower mutation frequencies of TSC2, FGFR1, PTPN13, SMAD3, and STK11 than stage IV patients (p < 0.05). Sixty-three mutated genes were unique to stage II tumors, while 36 mutated genes were exclusively present in stage IV tumors. Pathway analyses demonstrated the PI3K-AKT pathway was shared by both stage II and stage IV tumors, whereas multiple other signaling pathways showed disease stage-specific enrichment.ConclusionThere were profound differences in mutational profile and molecular mechanisms between stage II and stage IV dMMR/MSI-H CRC.

目的高微卫星不稳定性(MSI-H)和错配修复缺陷(dMMR)的结直肠癌(CRC)患者具有不同的病理和不同的预后。本研究旨在探讨不同疾病分期dMMR/MSI-H结直肠癌患者基因表达谱的差异,探讨疾病进展的不同分子机制。方法回顾性分析47例dMMR/MSI-H型结直肠癌患者,其中II期27例,IV期20例。每位患者都有配对的肿瘤组织和白细胞样本,这些样本通过下一代测序(NGS)对416种癌症相关基因进行了分析。然后进行途径富集分析以分析疾病阶段特异性信号通路。结果47例dMMR/MSI-H CRC患者共检测到2878个突变位点,涉及378个突变基因。II期患者的SMARCA4、EPHA3、MTHFR、RAD50和PDGFRB突变频率显著高于IV期患者(p < 0.05)
{"title":"Comparison of the differentially enriched mutations/pathways between stage II and stage IV dMMR/MSI-H colorectal cancer.","authors":"Chun Han, Sisi Ye, Juan Li, Qian Qiao, Li Bai, Tingting Zhang","doi":"10.1177/00368504251412580","DOIUrl":"10.1177/00368504251412580","url":null,"abstract":"<p><p>ObjectiveColorectal cancer (CRC) patients with high microsatellite instability (MSI-H) and mismatch repair deficiency (dMMR) had heterogeneous pathology and distinct prognoses. This study aimed to examine the difference in the gene expression profile of dMMR/MSI-H CRC patients with different disease stages and explore the different molecular mechanisms of disease progression.MethodsA total of 47 patients with dMMR/MSI-H CRC were enrolled and retrospectively studied, including 27 stage II and 20 stage IV patients. Each patient had paired tumor tissue and white blood cell samples, which were analyzed by next-generation sequencing (NGS) of 416 cancer-relevant genes. Pathway enrichment analysis was then performed to analyze the disease stage-specific signaling pathways.ResultsA total of 2878 mutation sites, spanning 378 mutated genes, were detected from the 47 dMMR/MSI-H CRC patients. The mutation frequencies of SMARCA4, EPHA3, MTHFR, RAD50, and PDGFRB were significantly higher in stage II patients than in stage IV patients (<i>p</i> < 0.05), whereas the stage II patients had significantly lower mutation frequencies of TSC2, FGFR1, PTPN13, SMAD3, and STK11 than stage IV patients (<i>p</i> < 0.05). Sixty-three mutated genes were unique to stage II tumors, while 36 mutated genes were exclusively present in stage IV tumors. Pathway analyses demonstrated the PI3K-AKT pathway was shared by both stage II and stage IV tumors, whereas multiple other signaling pathways showed disease stage-specific enrichment.ConclusionThere were profound differences in mutational profile and molecular mechanisms between stage II and stage IV dMMR/MSI-H CRC.</p>","PeriodicalId":56061,"journal":{"name":"Science Progress","volume":"109 1","pages":"368504251412580"},"PeriodicalIF":2.9,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12783548/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145936190","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Wind turbine bearing fault classification identification based on optimized variational mode decomposition and convolutional neural network-bidirectional gated recurrent unit-Attention. 基于优化变分模态分解和卷积神经网络双向门控循环单元的风力机轴承故障分类识别
IF 2.9 4区 综合性期刊 Q2 MULTIDISCIPLINARY SCIENCES Pub Date : 2026-01-01 Epub Date: 2026-02-16 DOI: 10.1177/00368504261417929
Minan Tang, Zhanglong Tao, Changyou Wang, Hongjie Wang, Kaiyue Zhang, Chuntao Rao, Donaev Sardor

As a key core component of wind turbine generators, the rolling bearings in the gearbox directly affect the overall performance and reliability of the wind turbine generators. Accurate prediction and timely diagnosis can effectively improve the efficiency of the wind turbine generators. This paper takes the rolling bearing operation data as the research object and proposes a bearing fault classification research method based on the combination of variational mode decomposition (VMD) optimization and convolutional neural network-bidirectional gated recurrent unit (CNN-BiGRU)-Attention model. Firstly, to address the sensitivity of intrinsic mode function (IMF) components in the VMD decomposition process, an improved RIEM algorithm is adopted to optimize the hyperparameters of the VMD algorithm. This process aims to adaptively adjust the penalty factor and decomposition layers of the VMD algorithm and find the optimal IMF component to determine the most suitable IMF component in the signal data. Secondly, to fully explore the complex characteristics of fault signals, composite multi-scale slope entropy is used to extract features from the optimized input data. By conducting multidimensional analysis on the local and global characteristics of the signal at different time scales, efficient representation of fault features is achieved. Finally, based on MATLAB, a simulation experiment platform is established. This paper conducts research on the classification of rolling bearing faults through the CNN-BiGRU-Attention model. The results show that the model established in this paper has significant effects and stable performance. The research in this paper provides new technical ideas for fault diagnosis of rolling bearings in wind turbine generator gear.

作为风力发电机组的关键核心部件,齿轮箱中的滚动轴承直接影响风力发电机组的整体性能和可靠性。准确的预测和及时的诊断可以有效地提高风力发电机组的效率。本文以滚动轴承运行数据为研究对象,提出了一种基于变分模态分解(VMD)优化与卷积神经网络-双向门控循环单元(CNN-BiGRU)-注意力模型相结合的轴承故障分类研究方法。首先,针对VMD分解过程中IMF分量的敏感性问题,采用改进的RIEM算法对VMD算法的超参数进行优化;该过程旨在自适应调整VMD算法的惩罚因子和分解层,找到最优的IMF分量,从而确定信号数据中最合适的IMF分量。其次,为了充分挖掘故障信号的复杂特征,利用复合多尺度斜率熵从优化后的输入数据中提取特征;通过对信号在不同时间尺度上的局部和全局特征进行多维度分析,实现故障特征的高效表示。最后,基于MATLAB搭建了仿真实验平台。本文通过CNN-BiGRU-Attention模型对滚动轴承故障分类进行了研究。结果表明,本文建立的模型效果显著,性能稳定。本文的研究为风电机组齿轮滚动轴承故障诊断提供了新的技术思路。
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引用次数: 0
ULK2 suppresses glycolysis to attenuate cisplatin resistance in ovarian cancer organoid via c-Jun phosphorylation. ULK2通过c-Jun磷酸化抑制糖酵解以减轻卵巢癌类器官的顺铂耐药性。
IF 2.9 4区 综合性期刊 Q2 MULTIDISCIPLINARY SCIENCES Pub Date : 2026-01-01 Epub Date: 2026-02-20 DOI: 10.1177/00368504261421695
Wei Chen, Xiaoxi Chen, Linlin Wang, Yaoyu Qu, Jin Zhao, Huizhen Sun

ObjectiveResistance to platinum-based chemotherapy remains a key obstacle in ovarian cancer treatment. This study aims to investigate the role of Uncoordinated 51-like kinase 2 (ULK2) in chemoresistance of ovarian cancer and elucidate its underlying mechanisms using 3D patient-derived organoids.MethodsSurvival analysis was first performed using the Kaplan‒Meier plotter database. Immunohistochemical profiling delineated differential ULK2 expression patterns between chemoresistant and chemosensitive ovarian cancer tissue samples and organoids. ULK2 overexpression was achieved in cisplatin-resistant ovarian cancer organoids via lentiviral vector transduction. Then, we conducted an in-depth examination of the alterations in phosphorylated proteins induced by ULK2 overexpression using phosphoproteomics technology. To investigate the influence of ULK2 on chemosensitivity in ovarian cancer, Cell Counting Kit-8 (CCK-8) and in vivo experiments were conducted. Glycolysis was quantitatively assessed, and the underlying molecular mechanism was systematically investigated.ResultsULK2 high-expression ovarian cancer exhibited enhanced chemosensitivity and conferred survival advantage. CCK-8 and mouse experiments demonstrated that ULK2 overexpression decreased cisplatin resistance in patient-derived organoids. Gene Ontology (GO) analysis of phosphoproteomics profiling highlighted the predominant role of ULK2 in metabolic processes with experimental validation demonstrating its suppression of glycolysis. Mechanistically, ULK2 attenuated c-Jun expression by phosphorylation of c-Jun at Ser243. Moreover, c-Jun overexpression counteracted the chemosensitivity and glycolytic suppression induced by the ectopic ULK2 expression in ovarian cancer.ConclusionsULK2 overcomes cisplatin resistance in ovarian cancer by downregulating glycolysis, a process mediated by phosphorylation-induced c-Jun degradation. These findings emphasized the role of ULK2 as a tumor suppressor, offering novel insights for chemotherapy in ovarian cancer.

目的对铂类化疗药物的耐药仍是卵巢癌治疗的主要障碍。本研究旨在探讨非协调51样激酶2 (ULK2)在卵巢癌化疗耐药中的作用,并利用3D患者来源的类器官阐明其潜在机制。方法采用Kaplan-Meier绘图仪数据库进行生存分析。免疫组织化学分析描述了化疗耐药和化疗敏感卵巢癌组织样本和类器官之间ULK2表达模式的差异。通过慢病毒载体转导,在顺铂耐药卵巢癌类器官中实现了ULK2的过表达。然后,我们使用磷酸化蛋白质组学技术对ULK2过表达诱导的磷酸化蛋白变化进行了深入研究。为了研究ULK2对卵巢癌化疗敏感性的影响,我们进行了细胞计数试剂盒-8 (CCK-8)和体内实验。对糖酵解进行了定量评估,并系统地研究了潜在的分子机制。结果sulk2高表达卵巢癌表现出更高的化疗敏感性和生存优势。CCK-8和小鼠实验表明,ULK2过表达可降低患者源性类器官的顺铂耐药性。磷酸化蛋白质组学的基因本体(GO)分析强调了ULK2在代谢过程中的主导作用,实验验证了它对糖酵解的抑制作用。从机制上讲,ULK2通过磷酸化c-Jun的Ser243位点来减弱c-Jun的表达。此外,c-Jun的过表达抵消了卵巢癌中异位ULK2表达引起的化疗敏感性和糖酵解抑制。结论sulk2通过下调糖酵解(一个由磷酸化诱导的c-Jun降解介导的过程)来克服卵巢癌的顺铂耐药。这些发现强调了ULK2作为肿瘤抑制因子的作用,为卵巢癌的化疗提供了新的见解。
{"title":"ULK2 suppresses glycolysis to attenuate cisplatin resistance in ovarian cancer organoid via c-Jun phosphorylation.","authors":"Wei Chen, Xiaoxi Chen, Linlin Wang, Yaoyu Qu, Jin Zhao, Huizhen Sun","doi":"10.1177/00368504261421695","DOIUrl":"10.1177/00368504261421695","url":null,"abstract":"<p><p>ObjectiveResistance to platinum-based chemotherapy remains a key obstacle in ovarian cancer treatment. This study aims to investigate the role of Uncoordinated 51-like kinase 2 (ULK2) in chemoresistance of ovarian cancer and elucidate its underlying mechanisms using 3D patient-derived organoids.MethodsSurvival analysis was first performed using the Kaplan‒Meier plotter database. Immunohistochemical profiling delineated differential ULK2 expression patterns between chemoresistant and chemosensitive ovarian cancer tissue samples and organoids. ULK2 overexpression was achieved in cisplatin-resistant ovarian cancer organoids via lentiviral vector transduction. Then, we conducted an in-depth examination of the alterations in phosphorylated proteins induced by ULK2 overexpression using phosphoproteomics technology. To investigate the influence of ULK2 on chemosensitivity in ovarian cancer, Cell Counting Kit-8 (CCK-8) and <i>in vivo</i> experiments were conducted. Glycolysis was quantitatively assessed, and the underlying molecular mechanism was systematically investigated.ResultsULK2 high-expression ovarian cancer exhibited enhanced chemosensitivity and conferred survival advantage. CCK-8 and mouse experiments demonstrated that ULK2 overexpression decreased cisplatin resistance in patient-derived organoids. Gene Ontology (GO) analysis of phosphoproteomics profiling highlighted the predominant role of ULK2 in metabolic processes with experimental validation demonstrating its suppression of glycolysis. Mechanistically, ULK2 attenuated c-Jun expression by phosphorylation of c-Jun at Ser243. Moreover, c-Jun overexpression counteracted the chemosensitivity and glycolytic suppression induced by the ectopic ULK2 expression in ovarian cancer.ConclusionsULK2 overcomes cisplatin resistance in ovarian cancer by downregulating glycolysis, a process mediated by phosphorylation-induced c-Jun degradation. These findings emphasized the role of ULK2 as a tumor suppressor, offering novel insights for chemotherapy in ovarian cancer.</p>","PeriodicalId":56061,"journal":{"name":"Science Progress","volume":"109 1","pages":"368504261421695"},"PeriodicalIF":2.9,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12924953/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146260133","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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