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Pancreatic Cancer Collagen-Based Optical Signatures

机译:基于胰腺癌的胰腺癌光学签名

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Cancer progression is closely related to changes in the structure and mechanical properties of the tumor microenvironment in a complex and not well-understood manner. In many solid tumors, including pancreatic cancer, the complex interplay among the different components of tumor microenvironment leads to a desmoplastic reaction associated with fibroblasts activation and collagen overproduction. Desmoplasia is responsible for tumor stiffening, and poses a major barrier to the effective delivery of drugs and has been associated with poor prognosis. Thus, the understanding of the involved mechanisms and the identification of collagen-based signatures that characterize the state of a particular tumor can lead to the development of novel diagnostic and prognostic biomarkers. In this study, pancreatic tumor models were developed employing the human pancreatic cancer cell lines BxPc-3 and MIAPaCa-2 and tissue biopsies were obtained at different stages of cancer progression. Polarized microscopy on picrosirius red stained tumor sections was used in order to assess collagen-based optical signatures in correlation with tumor progression, while Atomic Force Microscopy (AFM) was applied for the nano-mechanical characterization of the samples. The results demonstrated that pancreatic cancer presents unique collagen-based characteristics that can be used as a novel biomarker for cancer diagnosis and prognosis.
机译:癌症进展与肿瘤微环境的结构和力学性质的变化密切相关,以复杂且不良好地理解的方式。在许多实体肿瘤中,包括胰腺癌,肿瘤微环境不同组分之间的复杂相互作用导致与成纤维细胞活化和胶原过度产生相关的脱模反应。 Desmoplasia负责肿瘤加强,并对药物有效递送的主要屏障构成,并与预后差有关。因此,了解所涉及的机制和鉴定表征特定肿瘤状态的基于胶原的签名可以导致新型诊断和预后生物标志物的发育。在这项研究中,开发了胰腺癌模型,采用人胰腺癌细胞系BXPC-3和MIAPACA-2和组织活组织检查在癌症进展的不同阶段获得。使用PICROSIRIUS红色染色肿瘤切片上的偏振显微镜,以评估基于胶原的光学签名与肿瘤进展相关,而原子力显微镜(AFM)被应用于样品的纳米机械表征。结果表明,胰腺癌呈现出独特的基于胶原蛋白的特征,可用作癌症诊断和预后的新型生物标志物。

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