Jen-Tai Lin , Ya-Ping Chung , Tong-Lin Wu , Wan-Ching Lin , Balasubramanian Sriram , Sea-Fue Wang , Sekhar Praveen , Thiagarajan Soundappan , Sakthivel Kogularasu , Guo-Ping Chang-Chien
{"title":"授权前列腺癌的早期检测:一个点护理生物传感的观点","authors":"Jen-Tai Lin , Ya-Ping Chung , Tong-Lin Wu , Wan-Ching Lin , Balasubramanian Sriram , Sea-Fue Wang , Sekhar Praveen , Thiagarajan Soundappan , Sakthivel Kogularasu , Guo-Ping Chang-Chien","doi":"10.1016/j.microc.2025.114538","DOIUrl":null,"url":null,"abstract":"<div><div>Prostate cancer (PCa) is a major oncological burden globally, with disease progression closely linked to the timeliness and accuracy of clinical detection. Despite widespread use, conventional diagnostic approaches, including prostate-specific antigen assays, digital rectal examination, and ultrasound-guided biopsy, suffer from significant limitations such as poor biomarker specificity, invasiveness, and inter-operator variability, contributing to overdiagnosis and overtreatment. Recent advances in biosensor engineering have enabled the development of highly sensitive, selective, and multiplexed point-of-care diagnostic systems that can quantitatively detect PCa-associated biomarkers in noninvasive biological fluids with minimal sample processing. This review critically examines the current landscape of POC biosensing strategies for PCa, focusing on electrochemical, optical, and field-effect transistor (FET)-based platforms functionalized with high-affinity biorecognition elements such as antibodies, aptamers, and synthetic receptors. We highlight clinically validated and emerging molecular targets, including PSA isoforms, PCA3, TMPRSS2–ERG fusion transcripts, exosomal RNAs, and circulating tumor cells, and evaluate their diagnostic performance in integrated sensor systems. Emphasis is placed on the role of nanostructured transducer interfaces such as graphene, MXenes, metal–organic frameworks, and quantum dots in enhancing signal-to-noise ratios, lowering detection limits to the femtomolar range, and enabling multimodal sensing. Moreover, the integration of machine learning (ML) and explainable artificial intelligence (XAI) algorithms into biosensor data workflows is discussed as a means to extract clinically actionable insights from high-dimensional, multi-biomarker datasets. These intelligent systems facilitate individualized risk assessment, improved classification of equivocal cases, and data-driven clinical decision-making. Finally, we address translational challenges related to device reproducibility, regulatory compliance, long-term stability, and deployment in low-resource settings. Collectively, the synergy between advanced materials, real-time analytics, and noninvasive sample access positions next-generation biosensing technologies as a cornerstone in the future of precision diagnostics and global prostate cancer management.</div></div>","PeriodicalId":391,"journal":{"name":"Microchemical Journal","volume":"215 ","pages":"Article 114538"},"PeriodicalIF":4.9000,"publicationDate":"2025-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Empowering early detection of prostate cancer: a point-of-care biosensing perspective\",\"authors\":\"Jen-Tai Lin , Ya-Ping Chung , Tong-Lin Wu , Wan-Ching Lin , Balasubramanian Sriram , Sea-Fue Wang , Sekhar Praveen , Thiagarajan Soundappan , Sakthivel Kogularasu , Guo-Ping Chang-Chien\",\"doi\":\"10.1016/j.microc.2025.114538\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Prostate cancer (PCa) is a major oncological burden globally, with disease progression closely linked to the timeliness and accuracy of clinical detection. Despite widespread use, conventional diagnostic approaches, including prostate-specific antigen assays, digital rectal examination, and ultrasound-guided biopsy, suffer from significant limitations such as poor biomarker specificity, invasiveness, and inter-operator variability, contributing to overdiagnosis and overtreatment. Recent advances in biosensor engineering have enabled the development of highly sensitive, selective, and multiplexed point-of-care diagnostic systems that can quantitatively detect PCa-associated biomarkers in noninvasive biological fluids with minimal sample processing. This review critically examines the current landscape of POC biosensing strategies for PCa, focusing on electrochemical, optical, and field-effect transistor (FET)-based platforms functionalized with high-affinity biorecognition elements such as antibodies, aptamers, and synthetic receptors. We highlight clinically validated and emerging molecular targets, including PSA isoforms, PCA3, TMPRSS2–ERG fusion transcripts, exosomal RNAs, and circulating tumor cells, and evaluate their diagnostic performance in integrated sensor systems. Emphasis is placed on the role of nanostructured transducer interfaces such as graphene, MXenes, metal–organic frameworks, and quantum dots in enhancing signal-to-noise ratios, lowering detection limits to the femtomolar range, and enabling multimodal sensing. Moreover, the integration of machine learning (ML) and explainable artificial intelligence (XAI) algorithms into biosensor data workflows is discussed as a means to extract clinically actionable insights from high-dimensional, multi-biomarker datasets. These intelligent systems facilitate individualized risk assessment, improved classification of equivocal cases, and data-driven clinical decision-making. Finally, we address translational challenges related to device reproducibility, regulatory compliance, long-term stability, and deployment in low-resource settings. Collectively, the synergy between advanced materials, real-time analytics, and noninvasive sample access positions next-generation biosensing technologies as a cornerstone in the future of precision diagnostics and global prostate cancer management.</div></div>\",\"PeriodicalId\":391,\"journal\":{\"name\":\"Microchemical Journal\",\"volume\":\"215 \",\"pages\":\"Article 114538\"},\"PeriodicalIF\":4.9000,\"publicationDate\":\"2025-07-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Microchemical Journal\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0026265X25018922\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microchemical Journal","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0026265X25018922","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Empowering early detection of prostate cancer: a point-of-care biosensing perspective
Prostate cancer (PCa) is a major oncological burden globally, with disease progression closely linked to the timeliness and accuracy of clinical detection. Despite widespread use, conventional diagnostic approaches, including prostate-specific antigen assays, digital rectal examination, and ultrasound-guided biopsy, suffer from significant limitations such as poor biomarker specificity, invasiveness, and inter-operator variability, contributing to overdiagnosis and overtreatment. Recent advances in biosensor engineering have enabled the development of highly sensitive, selective, and multiplexed point-of-care diagnostic systems that can quantitatively detect PCa-associated biomarkers in noninvasive biological fluids with minimal sample processing. This review critically examines the current landscape of POC biosensing strategies for PCa, focusing on electrochemical, optical, and field-effect transistor (FET)-based platforms functionalized with high-affinity biorecognition elements such as antibodies, aptamers, and synthetic receptors. We highlight clinically validated and emerging molecular targets, including PSA isoforms, PCA3, TMPRSS2–ERG fusion transcripts, exosomal RNAs, and circulating tumor cells, and evaluate their diagnostic performance in integrated sensor systems. Emphasis is placed on the role of nanostructured transducer interfaces such as graphene, MXenes, metal–organic frameworks, and quantum dots in enhancing signal-to-noise ratios, lowering detection limits to the femtomolar range, and enabling multimodal sensing. Moreover, the integration of machine learning (ML) and explainable artificial intelligence (XAI) algorithms into biosensor data workflows is discussed as a means to extract clinically actionable insights from high-dimensional, multi-biomarker datasets. These intelligent systems facilitate individualized risk assessment, improved classification of equivocal cases, and data-driven clinical decision-making. Finally, we address translational challenges related to device reproducibility, regulatory compliance, long-term stability, and deployment in low-resource settings. Collectively, the synergy between advanced materials, real-time analytics, and noninvasive sample access positions next-generation biosensing technologies as a cornerstone in the future of precision diagnostics and global prostate cancer management.
期刊介绍:
The Microchemical Journal is a peer reviewed journal devoted to all aspects and phases of analytical chemistry and chemical analysis. The Microchemical Journal publishes articles which are at the forefront of modern analytical chemistry and cover innovations in the techniques to the finest possible limits. This includes fundamental aspects, instrumentation, new developments, innovative and novel methods and applications including environmental and clinical field.
Traditional classical analytical methods such as spectrophotometry and titrimetry as well as established instrumentation methods such as flame and graphite furnace atomic absorption spectrometry, gas chromatography, and modified glassy or carbon electrode electrochemical methods will be considered, provided they show significant improvements and novelty compared to the established methods.