MEANS AND METHODS FOR DIAGNOSING PANCREATIC CANCER IN A SUBJECT BASED ON A BIOMARKER PANEL
    3.
    发明申请
    MEANS AND METHODS FOR DIAGNOSING PANCREATIC CANCER IN A SUBJECT BASED ON A BIOMARKER PANEL 审中-公开
    用于诊断基于生物标记物面板的主体中的胰腺癌的手段和方法

    公开(公告)号:WO2016207391A1

    公开(公告)日:2016-12-29

    申请号:PCT/EP2016/064736

    申请日:2016-06-24

    Abstract: The present invention relates to a method for diagnosing pancreatic cancer in a subject comprising the steps of: (a) determining in at least one sample of said subject the amounts of a group of diagnostic biomarkers comprising (i) at least one diagnostic amino acid, said diagnostic amino acid being proline, histidine or tryptophan, preferably, being proline; (ii) at least one diagnostic ceramide, said diagnostic ceramide being ceramide (d18:1,C24:0) or ceramide (d18:2,C24:0), preferably being ceramide (d18:1,C24:0); (iii) at least one diagnostic sphingomyelin, said diagnostic sphingomyelin being sphingomyelin (35:1), sphingomyelin (d17:1,C16:0), sphingomyelin (41 :2) or sphingomyelin (d18:2,C17:0), preferably being sphingomyelin (35:1); and (iv) CA19-9; and (b) comparing said amounts of the diagnostic biomarkers with a reference, whereby pancreatic cancer is diagnosed. Moreover, the present invention relates to a method for determining the probability for a subject to suffer from pancreatic cancer, and to devices and uses related to said methods.

    Abstract translation: 本发明涉及一种用于诊断受试者的胰腺癌的方法,包括以下步骤:(a)在所述受试者的至少一个样品中测定一组诊断性生物标志物的量,所述诊断生物标志物组包含(i)至少一种诊断性氨基酸, 所述诊断性氨基酸为脯氨酸,组氨酸或色氨酸,优选为脯氨酸; (ii)至少一种诊断性神经酰胺,所述诊断性神经酰胺为神经酰胺(d18:1,C24:0)或神经酰胺(d18:2,C24:0),优选为神经酰胺(d18:1,C24:0); (iii)至少一种诊断性鞘磷脂,所述诊断性鞘磷脂是鞘磷脂(35:1),鞘磷脂(d17:1,C16:0),鞘磷脂(41:2)或鞘磷脂(d18:2,C17:0) 是鞘磷脂(35:1); 和(iv)CA19-9; 和(b)将所述诊断生物标志物的量与参考文献进行比较,由此诊断胰腺癌。 此外,本发明涉及一种用于确定受试者患有胰腺癌的可能性的方法以及与所述方法相关的装置和用途。

    BIOMAKERS OF DE NOVO LIPOGENESIS AND METHODS USING THE SAME
    6.
    发明申请
    BIOMAKERS OF DE NOVO LIPOGENESIS AND METHODS USING THE SAME 审中-公开
    DE NOVO生物制品生物制品及其使用方法

    公开(公告)号:WO2015095451A1

    公开(公告)日:2015-06-25

    申请号:PCT/US2014/071035

    申请日:2014-12-18

    CPC classification number: G01N33/92 G01N2405/00 G01N2800/7085

    Abstract: Biomarkers relating to de novo lipogenesis are provided, as well as methods for using such biomarkers in an Index to assess DNL. In addition, methods for diagnosing, determining predisposition to, and monitoring progression/regression of diseases related to DNL are provided. Also provided are methods of monitoring the efficacy of treatments for diseases related to DNL as well as other methods based on biomarkers of DNL.

    Abstract translation: 提供与新生脂肪生成有关的生物标志物,以及在索引中使用这些生物标志物评估DNL的方法。 此外,还提供了诊断,确定与DNL相关疾病的倾向和监测进展/退化的方法。 还提供了监测与DNL相关疾病的治疗功效以及基于DNL生物标志物的其它方法的方法。

    METHODS AND COMPOSITIONS FOR IDENTIFYING NON-ALCOHOLIC FATTY LIVER DISEASE
    9.
    发明申请
    METHODS AND COMPOSITIONS FOR IDENTIFYING NON-ALCOHOLIC FATTY LIVER DISEASE 审中-公开
    鉴定非酒精性脂肪肝疾病的方法和组合

    公开(公告)号:WO2016130961A1

    公开(公告)日:2016-08-18

    申请号:PCT/US2016/017822

    申请日:2016-02-12

    Abstract: The disclosure provides methods for differentiating between non-alcoholic fatty liver disease and non-alcoholic steatohepatitis. The method includes measuring eicosanoids and fatty acid levels in a biological sample. The disclosure provides a method of differentiating nonalcoholic steatohepatitis (NASH) from nonalcoholic fatty liver (NAFL) in a subject. The method includes obtaining a biological sample from the subject; treating the sample with an alkaline solution to release esterified eicosanoids and recovering the eicosanoids; and comparing the levels of at least one esterified eicosanoid in the biological sample obtained from the subject to a control sample obtained from a NAFL subject, wherein a difference in the levels of the at least one eicosanoid in the sample obtained from the subject compared to the control is indicative of NASH.

    Abstract translation: 本公开提供了用于区分非酒精性脂肪肝疾病和非酒精性脂肪性肝炎的方法。 该方法包括测量生物样品中的类二十烷酸和脂肪酸水平。 本公开提供了在受试者中区分非酒精性脂肪性肝炎(NASH)与非酒精性脂肪肝(NAFL)的方法。 该方法包括从受试者获得生物样品; 用碱性溶液处理样品以释放酯化的类花生酸并回收类花生酸; 并将从受试者获得的生物样品中的至少一种酯化类花生酸的水平与从NAFL受试者获得的对照样品进行比较,其中从受试者获得的样品中的至少一种类花生酸的水平与 控制指示NASH。

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