DTC, differentiated thyroid cancer

  • 文章类型: Journal Article
    甲状腺癌,作为最常见的内分泌癌症之一,近年来发病率激增。这很可能是由于其传统诊断方式缺乏特异性和准确性,导致甲状腺结节的过度诊断。虽然有几种治疗选择,它们仅限于手术和131I放射治疗,这些治疗具有显著的副作用,因此不能满足恶性程度非常高的未分化甲状腺癌的治疗需求.利用光吸收的光学成像,折射和散射特性,不仅观察细胞的结构和功能,组织,器官,甚至整个有机体来协助诊断,但也可用于进行光学治疗,以实现甲状腺癌的靶向非侵入性和精确治疗。这些筛选的应用,诊断,和治疗,赋予光学成像在甲状腺癌手术导航领域的潜力。在过去的十年里,光学成像在甲状腺癌诊断和治疗中的研究逐年增长,但是没有发表关于这个主题的全面评论。这里,我们回顾了光学成像在甲状腺癌诊断和治疗中应用的关键进展,并讨论了该技术在临床应用中的挑战和潜力。
    Thyroid cancer, as one of the most common endocrine cancers, has seen a surge in incidence in recent years. This is most likely due to the lack of specificity and accuracy of its traditional diagnostic modalities, leading to the overdiagnosis of thyroid nodules. Although there are several treatment options available, they are limited to surgery and 131I radiation therapy that come with significant side effects and hence cannot meet the treatment needs of anaplastic thyroid carcinoma with very high malignancy. Optical imaging that utilizes optical absorption, refraction and scattering properties, not only observes the structure and function of cells, tissues, organs, or even the whole organism to assist in diagnosis, but can also be used to perform optical therapy to achieve targeted non-invasive and precise treatment of thyroid cancer. These applications of screening, diagnosis, and treatment, lend to optical imaging\'s promising potential within the realm of thyroid cancer surgical navigation. Over the past decade, research on optical imaging in the diagnosis and treatment of thyroid cancer has been growing year by year, but no comprehensive review on this topic has been published. Here, we review key advances in the application of optical imaging in the diagnosis and treatment of thyroid cancer and discuss the challenges and potential for clinical translation of this technology.
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  • 文章类型: Journal Article
    未经评估:尽管其明显优于基于免疫测定的测试,通过质谱法测量血清甲状腺球蛋白仍然局限于少数机构。临床实验室的缓慢采用可能反映出现有方法的可及性有限,这些方法具有与现代免疫测定相当的灵敏度,以及缺乏校准和分析协调的工具。
    UNASSIGNED:我们开发并验证了一种基于液相色谱-串联质谱的血清甲状腺球蛋白定量检测方法。该方案结合肽免疫亲和纯化使用市售,充分表征的单克隆抗体和流动相修饰与二甲亚砜(DMSO)增强的灵敏度。为了促进与其他实验室的协调,我们开发了一部小说,基于血清的5点可分配参考材料(HuskyRef)。
    UNASSIGNED:该测定显示0.15ng/mL(<20%CV)的定量下限。流动相DMSO使靶肽的信号强度增加至少3倍,改善低浓度的定量。可追溯到HuskyRef的校准使实验室间研究中的实验室之间得以协调。
    UNASSIGNED:在肽免疫亲和纯化和添加流动相DMSO的过程中,可以使用单克隆抗体实现基于质谱的灵敏甲状腺球蛋白测量。有兴趣部署此测定的实验室可以利用提供的标准操作程序和免费获得的HuskyRef参考材料。
    UNASSIGNED: Despite its clear advantages over immunoassay-based testing, the measurement of serum thyroglobulin by mass spectrometry remains limited to a handful of institutions. Slow adoption by clinical laboratories could reflect limited accessibility to existing methods that have sensitivity comparable to modern immunoassays, as well as a lack of tools for calibration and assay harmonization.
    UNASSIGNED: We developed and validated a liquid chromatography-tandem mass spectrometry-based assay for the quantification of serum thyroglobulin. The protocol combined peptide immunoaffinity purification using a commercially available, well-characterized monoclonal antibody and mobile phase modification with dimethylsulfoxide (DMSO) for enhanced sensitivity. To facilitate harmonization with other laboratories, we developed a novel, serum-based 5-point distributable reference material (Husky Ref).
    UNASSIGNED: The assay demonstrated a lower limit of quantification of 0.15 ng/mL (<20 %CV). Mobile phase DMSO increased signal intensity of the target peptide at least 3-fold, improving quantification at low concentrations. Calibration traceable to Husky Ref enabled harmonization between laboratories in an interlaboratory study.
    UNASSIGNED: Sensitive mass spectrometry-based thyroglobulin measurement can be achieved using a monoclonal antibody during peptide immunoaffinity purification and the addition of mobile phase DMSO. Laboratories interested in deploying this assay can utilize the provided standard operating procedure and freely-available Husky Ref reference material.
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  • 文章类型: Journal Article
    癌细胞重新编程其基因表达以促进生长,生存,扩散,和侵入性。某些摄取转运蛋白在癌症中的独特表达及其在细胞中浓缩小分子底物的先天功能使其成为选择性递送成像和治疗剂进入癌细胞的理想靶标。在这次审查中,我们专注于几种已知参与将临床使用的放射性药物运输到癌细胞中的溶质载体(SLC)转运蛋白,包括钠/碘同向转运蛋白(NIS),去甲肾上腺素转运蛋白(NET),葡萄糖转运蛋白1(GLUT1),和单羧酸盐转运蛋白(MCT)。审查了这些转运蛋白的分子和功能特征,特别强调了它们在癌症中的特定表达以及与成像或治疗诊断药物的相互作用[例如,I-123,I-131,123I-iobenguane(mIBG),18F-氟代脱氧葡萄糖(18F-FDG)和13C丙酮酸盐]。讨论了这些转运蛋白在癌症诊断和治疗中的临床应用和研究领域。最后,我们就靶向转运蛋白用于癌症成像和治疗的新机会和挑战提出了我们的观点.通过分析几个临床上成功的例子,我们希望对摄取转运蛋白及其在癌症诊断和治疗中的潜在应用的癌症研究能够引起更多的兴趣。
    Cancer cells reprogram their gene expression to promote growth, survival, proliferation, and invasiveness. The unique expression of certain uptake transporters in cancers and their innate function to concentrate small molecular substrates in cells make them ideal targets for selective delivering imaging and therapeutic agents into cancer cells. In this review, we focus on several solute carrier (SLC) transporters known to be involved in transporting clinically used radiopharmaceutical agents into cancer cells, including the sodium/iodine symporter (NIS), norepinephrine transporter (NET), glucose transporter 1 (GLUT1), and monocarboxylate transporters (MCTs). The molecular and functional characteristics of these transporters are reviewed with special emphasis on their specific expressions in cancers and interaction with imaging or theranostic agents [e.g., I-123, I-131, 123I-iobenguane (mIBG), 18F-fluorodeoxyglucose (18F-FDG) and 13C pyruvate]. Current clinical applications and research areas of these transporters in cancer diagnosis and treatment are discussed. Finally, we offer our views on emerging opportunities and challenges in targeting transporters for cancer imaging and treatment. By analyzing the few clinically successful examples, we hope much interest can be garnered in cancer research towards uptake transporters and their potential applications in cancer diagnosis and treatment.
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