1.Novel hormone therapies for advanced prostate cancer: Understanding and countering drug resistance.
Zhipeng WANG ; Jie WANG ; Dengxiong LI ; Ruicheng WU ; Jianlin HUANG ; Luxia YE ; Zhouting TUO ; Qingxin YU ; Fanglin SHAO ; Dilinaer WUSIMAN ; William C CHO ; Siang Boon KOH ; Wei XIONG ; Dechao FENG
Journal of Pharmaceutical Analysis 2025;15(9):101232-101232
Prostate cancer is the most prevalent malignant tumor among men, ranking first in incidence and second in mortality globally. Novel hormone therapies (NHT) targeting the androgen receptor (AR) pathway have become the standard of care for metastatic prostate cancer. This review offers a comprehensive overview of NHT, including abiraterone, enzalutamide, apalutamide, darolutamide, and rezvilutamide, which have demonstrated efficacy in delaying disease progression and improving patient survival and quality of life. Nevertheless, resistance to NHT remains a critical challenge. The mechanisms underlying resistance are complex, involving AR gene amplification, mutations, splice variants, increased intratumoral androgens, and AR-independent pathways such as the glucocorticoid receptor, neuroendocrine differentiation, DNA repair defects, autophagy, immune evasion, and activation of alternative signaling pathways. This review discusses these resistance mechanisms and examines strategies to counteract them, including sequential treatment with novel AR-targeted drugs, chemotherapy, poly ADP-ribose polymerase inhibitors, radionuclide therapy, bipolar androgen therapy, and approaches targeting specific resistance pathways. Future research should prioritize elucidating the molecular basis of NHT resistance, optimizing existing therapeutic strategies, and developing more effective combination regimens. Additionally, advanced sequencing technologies and resistance research models should be leveraged to identify novel therapeutic targets and improve drug delivery efficiencies. These advancements hold the potential to overcome NHT resistance and significantly enhance the management and prognosis of patients with advanced prostate cancer.
2.Boosting prediction of occupational stress among manufacturing employees by reconstructing cumulative fatigue features with Bayesian sparse autoencoder
Tao SONG ; Yuting ZHOU ; Xinyi LU ; Xinkai WEI ; Qingxin MENG ; Jianlin LOU ; Hongchang ZHOU ; Jin WANG ; Shuang LI
Journal of Environmental and Occupational Medicine 2025;42(12):1446-1455
Background Occupational stress has emerged as a critical public health concern affecting the physical and mental well-being of workers in the manufacturing sector. However, researchers typically evaluate its core driver—cumulative fatigue—using a crude binary “present/absent” variable, thereby overlooking the high-dimensional complexity and heterogeneity inherent in fatigue characteristics. This oversimplification constrains both the precision and predictive performance of occupational stress risk assessment model. Objective Leveraging a data-driven approach, to survey data on cumulative fatigue among manufacturing employees, and then use this new classification to develop and validate an occupational stress prediction model, with an ultimate aim of enhancing the accuracy and effectiveness of occupational stress assessment. Methods A set of cross-sectional survey data on
3.Dosimetric impact of dwell position spacing in three-dimensional interstitial brachytherapy plans for cervical cancer
Wenwen ZHANG ; Yuanjie CAO ; Jie CHEN ; Zhiyong YUAN ; Jiaming ZHANG ; Zhiyong CUI ; Zhirong ZHANG ; Wei WANG ; Qingxin WANG
Chinese Journal of Radiation Oncology 2025;34(5):476-481
Objective:To investigate the dosimetric impact of dwell position spacing in the design of three-dimensional (3D) interstitial brachytherapy plans for cervical cancer, and to provide a reference for selecting dwell spacing in clinical planning.Methods:A total of 15 patients with cervical cancer who underwent 3D interstitial brachytherapy at Tianjin Medical University Cancer Institute & Hospital between March 2022 and March 2024 were selected using simple random sampling. For each patient, 10 brachytherapy plans were generated with different dwell position spacings set at 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10 mm, respectively. Key parameters among different dwell spacings compared included D 90%, V 100%, V 200%, and V 300% for the high-risk clinical target volume (HRCTV); D 90% for the intermediate-risk clinical target volume (IRCTV); D 2 cm3 for organs at risk (OARs) (bladder, small intestine, colon, and rectum); and the total dwell time. Statistical analyses were performed using repeated measurement ANOVA or the Friedman test. Results:Among different dwell spacings, there were no statistically significant differences in HRCTV D 90%, HRCTV V 100%, bladder D 2 cm3, and rectum D 2 cm3 among different dwell spacings ( P=0.075, 0.061, 0.480, 0.639). All plans with dwell spacings ≤ 3 mm met clinical dose requirements. When the dwell spacing was set to 1 mm, HRCTV V 200% and V 300% had the smallest mean values, while IRCTV D 90% and total dwell time had the largest mean values; all differences were statistically significant ( P<0.05). When the dwell spacing was ≥6 mm, an increase in spacing led to a decrease in mean small intestine D 2 cm3, and total dwell time, but an increase in HRCTV V 200% and a decrease in IRCTV D 90%, with statistically significant differences compared to spacings of 1-4 mm ( P<0.05). When the dwell spacing was ≥8 mm, the median colon D 2 cm3 decreased, with statistically significant differences compared to spacings of 1-3 mm ( P<0.05). Conclusions:For 3D interstitial brachytherapy planning in cervical cancer, dwell position spacings ≤ 3 mm can meet clinical dose requirements, with 1 mm providing optimal target coverage. Spacings ≥6 mm / ≥8 mm can reduce radiation dose to the small intestine and colon, respectively, while also shortening dwell time.
4.Genotype and drug susceptibility phenotype analysis of carbapenem-resistant Enterobacter cloacae in Taizhou area
Haohao LI ; Donglian WANG ; Qingxin SHI ; Sufei YU ; Qingfeng YU ; Yingying CAI
Chinese Journal of Clinical Laboratory Science 2025;43(1):7-12
Objective To investigate the distribution of carbapenem-resistant genes and their drug susceptibility in vitro on carbapen-em-resistant Enterobacter cloacae(CRECC)in Taizhou area,and provide evidence for effective anti-infective treatment in clinical prac-tice.Methods Forty-seven strains of CRECC isolated from Enze Hospital,Taizhou Enze Medical Center(Group)and Luqiao Reha-bilitation Hospital during January 2015 and November 2022 were retrospectively analyzed.The enzyme types and resistance genes of carbapenemase were detected by the NG-Test Carba 5 and Carba-R Xpert,respectively,and the susceptibility of CERCC to common drugs was tested in vitro.Results Among 47 strains of CRECC,27 were detected to produce carbapenemase,including 24 producing New Delhi metallo-β-lactamase(NDM)type,1 producing both Klebsiella pneumoniae carbapenemase(KPC)and NDM types,and 2 producing imipenemase(IMP)type.One strain belonged to NDM genotype but no NDM enzyme type was detected.The CRECC strains had the highest sensitivity to polymyxin B(95.7%),followed by tigecycline(93.6%),fosfomycin(61.7%),and ceftazidime/avibac-tam(40.4%).In addition,the CRECC strains producing carbapenemase were more sensitive to polymyxin B,fosfomycin and aztreo-nam than those without producing carbapenemase.Conclusion The CRECC strains in Taizhou area are mainly NDM type,which has high sensitivity to polycolistin B,tigecycline and fosfomycin.NG-Test Carba 5 can not cover some strains that do not produce carbapen-emase or carry mutations in carbapenemase.
5.The role of T cells and PD-L1 in advanced non-small cell lung carcinoma
Nan ZHANG ; Qingxin WANG ; Qin ZHANG
China Modern Doctor 2025;63(16):22-25
Objective To explore the role of regulatory T cells and exosome programmed death-ligand 1(PD-L1)in the immunotherapy of advanced non-small cell lung carcinoma(NSCLC).Methods Sixty patients with advanced NSCLC who visited China Coast Guard Hospital of the People's Armed Police Force from March 2022 to June 2024 were selected and included in lung carcinoma group.Among them,there were 30 patients squamous cell carcinoma and 30 patients with non-squamous cell carcinoma.Sixty healthy individuals undergoing physical examinations during the same period were selected as control group.Patients in squamous cell carcinoma group were treated with sintilimab+paclitaxel+cisplatin,while patients in non-squamous cell carcinoma group were treated with sintilimab+pemetrexed+carboplatin.Therapeutic effects and blood index results of two groups of patients were evaluated.Results The red blood cell count,hemoglobin,white blood cell count,platelets,CD3+,CD4+,CD4/CD8 and PD-L1 of patients in lung carcinoma group were significantly lower than those in control group(P<0.05).The remission rate of patients in squamous cell carcinoma group was significantly higher than that in non-squamous cell carcinoma group(P<0.05).After treatment,white blood cell count,CD8+,and exosome PD-L1 of patients in squamous cell carcinoma group were significantly lower than those in non-squamous cell carcinoma group,while red blood cell count,hemoglobin,platelets,CD3+,CD4+,and CD4/CD8 were significantly higher than those in non-squamous cell carcinoma group(P<0.05).Conclusion There are differences in immune responses among different subtypes of lung carcinoma,and targeted treatment plans should be formulated based on pathological types.
6.The role of T cells and PD-L1 in advanced non-small cell lung carcinoma
Nan ZHANG ; Qingxin WANG ; Qin ZHANG
China Modern Doctor 2025;63(16):22-25
Objective To explore the role of regulatory T cells and exosome programmed death-ligand 1(PD-L1)in the immunotherapy of advanced non-small cell lung carcinoma(NSCLC).Methods Sixty patients with advanced NSCLC who visited China Coast Guard Hospital of the People's Armed Police Force from March 2022 to June 2024 were selected and included in lung carcinoma group.Among them,there were 30 patients squamous cell carcinoma and 30 patients with non-squamous cell carcinoma.Sixty healthy individuals undergoing physical examinations during the same period were selected as control group.Patients in squamous cell carcinoma group were treated with sintilimab+paclitaxel+cisplatin,while patients in non-squamous cell carcinoma group were treated with sintilimab+pemetrexed+carboplatin.Therapeutic effects and blood index results of two groups of patients were evaluated.Results The red blood cell count,hemoglobin,white blood cell count,platelets,CD3+,CD4+,CD4/CD8 and PD-L1 of patients in lung carcinoma group were significantly lower than those in control group(P<0.05).The remission rate of patients in squamous cell carcinoma group was significantly higher than that in non-squamous cell carcinoma group(P<0.05).After treatment,white blood cell count,CD8+,and exosome PD-L1 of patients in squamous cell carcinoma group were significantly lower than those in non-squamous cell carcinoma group,while red blood cell count,hemoglobin,platelets,CD3+,CD4+,and CD4/CD8 were significantly higher than those in non-squamous cell carcinoma group(P<0.05).Conclusion There are differences in immune responses among different subtypes of lung carcinoma,and targeted treatment plans should be formulated based on pathological types.
7.Genotype and drug susceptibility phenotype analysis of carbapenem-resistant Enterobacter cloacae in Taizhou area
Haohao LI ; Donglian WANG ; Qingxin SHI ; Sufei YU ; Qingfeng YU ; Yingying CAI
Chinese Journal of Clinical Laboratory Science 2025;43(1):7-12
Objective To investigate the distribution of carbapenem-resistant genes and their drug susceptibility in vitro on carbapen-em-resistant Enterobacter cloacae(CRECC)in Taizhou area,and provide evidence for effective anti-infective treatment in clinical prac-tice.Methods Forty-seven strains of CRECC isolated from Enze Hospital,Taizhou Enze Medical Center(Group)and Luqiao Reha-bilitation Hospital during January 2015 and November 2022 were retrospectively analyzed.The enzyme types and resistance genes of carbapenemase were detected by the NG-Test Carba 5 and Carba-R Xpert,respectively,and the susceptibility of CERCC to common drugs was tested in vitro.Results Among 47 strains of CRECC,27 were detected to produce carbapenemase,including 24 producing New Delhi metallo-β-lactamase(NDM)type,1 producing both Klebsiella pneumoniae carbapenemase(KPC)and NDM types,and 2 producing imipenemase(IMP)type.One strain belonged to NDM genotype but no NDM enzyme type was detected.The CRECC strains had the highest sensitivity to polymyxin B(95.7%),followed by tigecycline(93.6%),fosfomycin(61.7%),and ceftazidime/avibac-tam(40.4%).In addition,the CRECC strains producing carbapenemase were more sensitive to polymyxin B,fosfomycin and aztreo-nam than those without producing carbapenemase.Conclusion The CRECC strains in Taizhou area are mainly NDM type,which has high sensitivity to polycolistin B,tigecycline and fosfomycin.NG-Test Carba 5 can not cover some strains that do not produce carbapen-emase or carry mutations in carbapenemase.
8.Dosimetric impact of dwell position spacing in three-dimensional interstitial brachytherapy plans for cervical cancer
Wenwen ZHANG ; Yuanjie CAO ; Jie CHEN ; Zhiyong YUAN ; Jiaming ZHANG ; Zhiyong CUI ; Zhirong ZHANG ; Wei WANG ; Qingxin WANG
Chinese Journal of Radiation Oncology 2025;34(5):476-481
Objective:To investigate the dosimetric impact of dwell position spacing in the design of three-dimensional (3D) interstitial brachytherapy plans for cervical cancer, and to provide a reference for selecting dwell spacing in clinical planning.Methods:A total of 15 patients with cervical cancer who underwent 3D interstitial brachytherapy at Tianjin Medical University Cancer Institute & Hospital between March 2022 and March 2024 were selected using simple random sampling. For each patient, 10 brachytherapy plans were generated with different dwell position spacings set at 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10 mm, respectively. Key parameters among different dwell spacings compared included D 90%, V 100%, V 200%, and V 300% for the high-risk clinical target volume (HRCTV); D 90% for the intermediate-risk clinical target volume (IRCTV); D 2 cm3 for organs at risk (OARs) (bladder, small intestine, colon, and rectum); and the total dwell time. Statistical analyses were performed using repeated measurement ANOVA or the Friedman test. Results:Among different dwell spacings, there were no statistically significant differences in HRCTV D 90%, HRCTV V 100%, bladder D 2 cm3, and rectum D 2 cm3 among different dwell spacings ( P=0.075, 0.061, 0.480, 0.639). All plans with dwell spacings ≤ 3 mm met clinical dose requirements. When the dwell spacing was set to 1 mm, HRCTV V 200% and V 300% had the smallest mean values, while IRCTV D 90% and total dwell time had the largest mean values; all differences were statistically significant ( P<0.05). When the dwell spacing was ≥6 mm, an increase in spacing led to a decrease in mean small intestine D 2 cm3, and total dwell time, but an increase in HRCTV V 200% and a decrease in IRCTV D 90%, with statistically significant differences compared to spacings of 1-4 mm ( P<0.05). When the dwell spacing was ≥8 mm, the median colon D 2 cm3 decreased, with statistically significant differences compared to spacings of 1-3 mm ( P<0.05). Conclusions:For 3D interstitial brachytherapy planning in cervical cancer, dwell position spacings ≤ 3 mm can meet clinical dose requirements, with 1 mm providing optimal target coverage. Spacings ≥6 mm / ≥8 mm can reduce radiation dose to the small intestine and colon, respectively, while also shortening dwell time.
9.Rapid detection of Staphylococcus aureus and mecA gene by recombinase aided amplification combined with dual nucleic acid lateral flow strips
GUO Qingxin ; ZHU Zonglin ; WANG Jiawen
China Tropical Medicine 2024;24(12):1465-
Objective To shorten the detection time of Staphylococcus aureus (SA), this study established a rapid detection method for the thermostable nuclease nuc gene and mecA resistance gene of SA based on recombinase aided amplification (RAA) combined with lateral flow strips (LFS). Methods Efficient RAA primers and probes were designed and screened based on the conserved sequences of the nuc gene in the SA genome and the mecA gene on the staphylococcal SCCmec removable genetic element, and then, the reaction temperature and for the simultaneous detection of nuc and mecA genes by time of RAA-LFS were verified. Sensitivity, specificity, and comparison with quantitative real-time PCR (qPCR) were also assessed. A prospective evaluation was conducted using 52 vials of non-repeat positive blood cultures from two tertiary hospitals. Results The RAA-LFS was able to amplify both nuc and mecA genes under the reaction conditions of 20-45 °C for 15-30 minutes, with a detection limit of 10² CFU/mL. A total of 50 clinically isolated non-SA strains were validated with 100% specificity for both nuc and mecA genes. Of the 30 methicillin-resistant Staphylococcus aureus (MRSA) and 30 methicillin-susceptible Staphylococcus aureus (MSSA) strains preserved in our laboratory, all were positive for the nuc gene, and 30 strains were positive for the mecA gene. The positive and negative concordance rates with qPCR were both 100%, with a consistency test Kappa value of 1. In a prospective analysis of the 52 vials of positive blood cultures, the identification and antibiotic susceptibility test results of 16 strains of MSSA and 6 strains of MRSA showed a 100% concordance rate with the results obtained using the Mérieux VITEK-2 compact microbiological detection system. Conclusions We combined nucleic acid release agents, RAA, and lateral flow strips to develop a simple, rapid, and highly sensitive assay applicable for SA and mecA resistance gene detection in colonies or positive blood culture bottles.
10.Advances in research on the role and mechanism of ferroptosis in radiation-induced injury
Qingxin WANG ; Zhongqiu WANG ; Wei WANG ; Peiguo WANG
Chinese Journal of Radiological Medicine and Protection 2024;44(6):537-542
Radiotherapy plays an important role in the comprehensive treatment of malignant tumors. Radiation-induced injury (RII) of normal tissue in tumor patients receiving radiotherapy, to varying degrees, is the most common adverse reaction of radiotherapy and an important factor influencing the course of radiotherapy. However, there is a lack of efficient prevention and treatment measures for RII. Ferroptosis, a novel type of cell death, has been reported several times to be closely associated with normal tissue damage induced by radiotherapy. This paper reviews the advances in research on ferroptosis, as well as its mechanism and association with RII.

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