Stage-specific circulating transcriptomic and proteomic biomarkers and regulators in colorectal cancer: bridging affordable diagnostics and translational therapeutics.

IF 6.2 2区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY
Raajesh Anand Natarajan
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引用次数: 0

Abstract

Colorectal cancer (CRC) remains a leading cause of cancer-related mortality worldwide, driven largely by pronounced molecular heterogeneity and delayed clinical detection. Although high-throughput sequencing technologies have substantially advanced the understanding of CRC biology, their routine clinical implementation remains constrained by high costs, infrastructural requirements, and limited accessibility. This review addresses these translational barriers by systematically synthesizing circulating transcriptomic and proteomic biomarkers within a clinically scalable framework. Particular emphasis is placed on biomolecules detectable using reverse transcription-polymerase chain reaction (RT-PCR) and enzyme-linked immunosorbent assay (ELISA), two widely accessible platforms that underwent extensive global optimization during the COVID-19 pandemic and are readily adaptable to liquid biopsy workflows. Through a stage-resolved analysis, we identify 9 genomic and 7 proteomic biomarkers associated with early-stage (I-II) CRC, alongside 9 genomic and 4 proteomic biomarkers linked to advanced-stage (III-IV) disease progression. Beyond biomarker cataloging, these molecules are integrated with Cancer Hallmark pathways, clinical-stage associations, and available clinical trial evidence to evaluate their biological relevance and translational readiness. In addition, we summarize standardized operating procedure (SOP) considerations and multiplex detection strategies to improve assay reproducibility, scalability, and cross-border clinical implementation. Collectively, this review bridges molecular discovery with clinically deployable laboratory workflows and provides a translational roadmap for the development of affordable, liquid biopsy-based diagnostic strategies aimed at improving CRC detection, patient stratification, longitudinal monitoring, and early therapeutic intervention.

结直肠癌分期特异性循环转录组学和蛋白质组学生物标志物和调节因子:连接可负担的诊断和转化治疗。
结直肠癌(CRC)仍然是世界范围内癌症相关死亡的主要原因,主要是由于明显的分子异质性和延迟的临床检测。尽管高通量测序技术极大地促进了对结直肠癌生物学的理解,但其常规临床应用仍然受到高成本、基础设施要求和有限可及性的限制。本综述通过在临床可扩展的框架内系统地合成循环转录组和蛋白质组生物标志物来解决这些翻译障碍。特别强调的是使用逆转录聚合酶链反应(RT-PCR)和酶联免疫吸附测定(ELISA)检测的生物分子,这两个广泛使用的平台在COVID-19大流行期间进行了广泛的全球优化,并且很容易适应液体活检工作流程。通过分期分析,我们确定了与早期(I-II) CRC相关的9个基因组和7个蛋白质组学生物标志物,以及与晚期(III-IV)疾病进展相关的9个基因组和4个蛋白质组学生物标志物。除了生物标志物编目之外,这些分子还与癌症标志通路、临床阶段关联和现有临床试验证据相结合,以评估其生物学相关性和转化准备程度。此外,我们总结了标准化操作程序(SOP)的考虑因素和多重检测策略,以提高分析的可重复性、可扩展性和跨境临床实施。总的来说,本综述将分子发现与临床可部署的实验室工作流程联系起来,并为开发可负担得起的、基于液体活检的诊断策略提供了一个转化路线图,旨在改善CRC检测、患者分层、纵向监测和早期治疗干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
20.00
自引率
0.00%
发文量
25
审稿时长
>12 weeks
期刊介绍: Critical Reviews in Clinical Laboratory Sciences publishes comprehensive and high quality review articles in all areas of clinical laboratory science, including clinical biochemistry, hematology, microbiology, pathology, transfusion medicine, genetics, immunology and molecular diagnostics. The reviews critically evaluate the status of current issues in the selected areas, with a focus on clinical laboratory diagnostics and latest advances. The adjective “critical” implies a balanced synthesis of results and conclusions that are frequently contradictory and controversial.
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