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Pancreatic Cancer Diagnosis and Management: Has the Time Come to Prick the Bubble?

机译:胰腺癌的诊断和治疗:是时候戳破泡沫了吗?

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Pancreatic cancer (PC) is associated with poor prognosis and very dismal survival rates. The most effective possibility of cure is tumor resection, which is only possible in about 15% of patients diagnosed at early stages of disease progression. Recent whole-genome sequencing studies pointed genetic alterations in 12 core signaling pathways in PC. These observations hint at the possibility that the initial mutation in PC might appear nearly 20 years before any symptoms occur, suggesting that a large window of opportunity may exist for early detection. Biomarkers with the potential to identify pre-neoplastic disease or very early stages of cancer are of great promise to improve patient survival. The concept of liquid biopsy refers to a minimally invasive sampling and analysis of liquid biomarkers that can be isolated from body fluids, primarily blood, urine and saliva. A myriad of circulating molecules may be useful as tumor markers, including cell-free DNA (cfDNA), cell-free RNA (cfRNA), circulating tumor cells (CTC), circulating tumor proteins, and extracellular vesicles, more specifically exosomes. In this review, we discuss with more detail the potential role of exosomes in several aspects related to PC, from initiation to tumor progression and its applicability in early detection and treatment. Exosomes are small circulating extracellular vesicles of 50–150 nm in diameter released from the plasma membrane by almost all cells and exhibit some advantages over other biomarkers. Exosomes are central players of intercellular communication and they have been implicated in a series of biological process, including tumorigenesis, migration and metastasis. Several exosomal microRNAs and proteins have been observed to distinguish PC from benign pancreatic diseases and healthy controls. Besides their possible role in diagnosis, understanding exosomes functions in cancer has clarified the importance of microenvironment in PC progression as well as its influence in proliferation, metastasis and resistance to chemotherapy. Increasing knowledge on cancer exosomes provides valuable insights on new therapeutic targets and can potentially open new strategies to treat this disease. Continuous research is needed to ascertain the reliability of using exosomes and their content as potential biomarkers, so that, hopefully, in the near future, they will provide the opportunity for early diagnosis, treatment intervention and increase survival of PC patients.
机译:胰腺癌(PC)与不良预后和非常糟糕的生存率相关。最有效的治愈方法是切除肿瘤,仅在疾病进展的早期阶段被诊断出的患者中约有15%才有可能。最近的全基因组测序研究指出了PC中12个核心信号通路的遗传改变。这些观察结果暗示了PC的初始突变可能在出现任何症状之前将近20年出现,这表明早期检测可能存在很大的机会。具有识别肿瘤前疾病或癌症早期的潜力的生物标志物有望改善患者的生存率。液体活检的概念是指可以从体液(主要是血液,尿液和唾液)中分离出来的液体生物标志物的微创采样和分析。无数的循环分子可用作肿瘤标志物,包括无细胞DNA(cfDNA),无细胞RNA(cfRNA),循环肿瘤细胞(CTC),循环肿瘤蛋白和细胞外囊泡,更具体而言是外泌体。在这篇综述中,我们更详细地讨论了外泌体在与PC相关的几个方面的潜在作用,从开始到肿瘤进展及其在早期检测和治疗中的适用性。外泌体是直径几乎为50-150 nm的小型循环细胞外囊泡,几乎所有细胞都从质膜释放出来,与其他生物标志物相比,它们具有某些优势。外泌体是细胞间通讯的核心参与者,它们已经参与了一系列生物学过程,包括肿瘤发生,迁移和转移。已经观察到几种外泌体微小RNA和蛋白质可以将PC与良性胰腺疾病和健康对照区分开。除了在诊断中可能发挥的作用外,了解外泌体在癌症中的功能还阐明了微环境在PC进程中的重要性以及其对增殖,转移和对化疗耐药的影响。对癌症外泌体的了解的增加为新的治疗靶点提供了宝贵的见识,并可能为治疗该疾病打开新的策略。需要进行持续的研究来确定使用外泌体及其含量作为潜在生物标志物的可靠性,以便希望在不久的将来,它们将为早期诊断,治疗干预和增加PC患者的生存率提供机会。

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