CALPROTECTIN AND HEMOGLOBIN/HAPTOGLOBIN COMPLEX FROM STOOL SAMPLE TO ASSESS COLORECTAL CANCER
    1.
    发明申请
    CALPROTECTIN AND HEMOGLOBIN/HAPTOGLOBIN COMPLEX FROM STOOL SAMPLE TO ASSESS COLORECTAL CANCER 审中-公开
    CALPROTECTIN和HEMOGLOBIN / HAPTOGLOBIN复合物从STOOL样品到评估彩色癌

    公开(公告)号:US20110129860A1

    公开(公告)日:2011-06-02

    申请号:US12783256

    申请日:2010-05-19

    IPC分类号: G01N33/68

    摘要: The present invention relates to a method aiding in the assessment of colorectal cancer. The method especially is used in assessing the absence or presence of colorectal cancer in vitro. The method is for example practiced by analyzing biochemical markers, comprising measuring in a stool sample the concentration of the hemoglobin/haptoglobin complex and calprotectin and correlating the concentrations determined to the absence or presence of colorectal cancer. To further improve the assessment of colorectal cancer based on a method of this invention the level of one or more additional marker may be determined together with the hemoglobin/haptoglobin complex and calprotectin in a stool sample and be correlated to the absence or presence of colorectal cancer. The invention also relates to the use of a marker panel comprising the hemoglobin/haptoglobin complex and calprotectin in the early diagnosis of colorectal cancer and it teaches a kit for performing the method of the invention.

    摘要翻译: 本发明涉及一种协助评估结肠直肠癌的方法。 该方法特别用于评估体外存在或不存在结肠直肠癌。 该方法例如通过分析生物化学标记来实施,包括在粪便样品中测量血红蛋白/触珠蛋白复合物和钙卫蛋白的浓度,并将确定的浓度与不存在或存在结肠直肠癌相关联。 为了进一步改进基于本发明方法的结肠直肠癌的评估,可以在粪便样品中与血红蛋白/触珠蛋白复合物和钙卫蛋白一起测定一种或多种另外的标记物的水平,并与结肠直肠癌的存在或不存在相关 。 本发明还涉及包含血红蛋白/触珠蛋白复合物和钙卫蛋白的标记物在早期诊断结肠直肠癌中的用途,并且其教导了用于实施本发明方法的试剂盒。

    MARKER PANEL FOR COLORECTAL CANCER
    2.
    发明申请
    MARKER PANEL FOR COLORECTAL CANCER 审中-公开
    用于彩色癌症的标记面板

    公开(公告)号:US20100240068A1

    公开(公告)日:2010-09-23

    申请号:US12791929

    申请日:2010-06-02

    IPC分类号: G01N33/573

    CPC分类号: G01N33/57419

    摘要: The present invention relates to a method for assessing colorectal cancer (CRC) in vitro including measuring in a sample the concentration and/or activity of a seprase polypeptide and/or fragments thereof and of either anti-p53 and/or osteopontin and/or ferritin, of optionally one or more other marker of CRC, and using the combined measurement result in the assessment of CRC. Furthermore, it especially relates to a method for assessing CRC from a liquid sample, derived from an individual by measuring seprase and at least anti-p53, ferritin and/or osteopontin in the sample. The method according to the present invention can, e.g., be used in the early detection of cancer by screening of asymptomatic individuals or in the surveillance of patients who undergo surgery.

    摘要翻译: 本发明涉及体外评估结肠直肠癌(CRC)的方法,包括在样品中测量seprase多肽和/或其片段和抗p53和/或骨桥蛋白和/或铁蛋白的浓度和/或活性 ,可选地一个或多个CRC的其他标志物,并且使用组合的测量结果来评估CRC。 此外,它特别涉及通过测量样品中的seprase和至少抗p53,铁蛋白和/或骨桥蛋白来评估来自个体的液体样品的CRC的方法。 根据本发明的方法可以例如通过筛选无症状个体或在进行手术的患者的监视中用于癌症的早期检测。

    ASSESSING COLORECTAL CANCER BY MEASURING OSTEOPONTIN AND CARCINOEMBRYONIC ANTIGEN
    4.
    发明申请
    ASSESSING COLORECTAL CANCER BY MEASURING OSTEOPONTIN AND CARCINOEMBRYONIC ANTIGEN 审中-公开
    通过测量OSTEOPONTIN和CARCINOEMBRYONIC ANTIGEN评估色素性癌

    公开(公告)号:US20090075312A1

    公开(公告)日:2009-03-19

    申请号:US12141278

    申请日:2008-06-18

    IPC分类号: C12Q1/48 G01N33/00

    摘要: The present invention relates to a method aiding in the assessment of colorectal cancer (=CRC). It discloses the use of a marker combination comprising osteopontin and carcinoembryonic antigen in the assessment of colorectal cancer. Furthermore, it especially relates to a method for assessing colorectal cancer from a liquid sample, derived from an individual by measuring at least the markers osteopontin and carcinoembryonic antigen in said sample. The marker combination comprising osteopontin and carcinoembryonic antigen can, e.g., be used in the early detection of colorectal cancer or in the surveillance of patients who undergo therapy, e.g., surgery.

    摘要翻译: 本发明涉及一种协助评估结肠直肠癌(= CRC)的方法。 它公开了在评估结肠直肠癌中使用包含骨桥蛋白和癌胚抗原的标记物组合。 此外,它特别涉及通过至少测量所述样品中的骨桥蛋白和癌胚抗原来评估来自个体的来自液体样品的结肠直肠癌的方法。 包括骨桥蛋白和癌胚抗原的标记物组合可以例如用于结肠直肠癌的早期检测或用于进行例如手术治疗的患者的监视。

    Assessing risk of disease progression in rheumatoid arthritis patients
    7.
    发明授权
    Assessing risk of disease progression in rheumatoid arthritis patients 有权
    评估类风湿关节炎患者疾病进展的风险

    公开(公告)号:US08058013B2

    公开(公告)日:2011-11-15

    申请号:US12412840

    申请日:2009-03-27

    IPC分类号: G01N33/53

    摘要: Disclosed is an in vitro method aiding in the further assessment of patients suffering from rheumatoid arthritis. The method especially is used in assessing whether an RA patient is at risk of disease progression. The method is for example practiced by analyzing biochemical markers, comprising measuring in a sample the concentration of at least C-reactive protein (CRP) and interleukin-6 and correlating the concentrations determined to the likelihood of an underlying rapidly progressing form of RA. A patient at high risk of a rapidly progressing disease might be a patient in need for treatment or if already treated in need for a different and more effective treatment. The invention also relates to the use of a marker panel comprising C-reactive protein and interleukin-6 in the assessment of a patient with rheumatoid arthritis and it teaches a protein array device and kit, respectively, for performing the method of the invention.

    摘要翻译: 公开了一种辅助进一步评估患有类风湿性关节炎患者的体外方法。 该方法特别用于评估RA患者是否处于疾病进展的风险。 该方法例如通过分析生物化学标记来实施,包括在样品中测量至少C反应蛋白(CRP)和白细胞介素-6的浓度,并将确定的浓度与RA的潜在快速进展形式的可能性相关联。 患有快速进展疾病的高风险患者可能是需要治疗的患者,或者如果已经需要治疗,需要进行不同的和更有效的治疗。 本发明还涉及在评估类风湿性关节炎患者中使用包含C-反应蛋白和白细胞介素-6的标记物片,并分别教导了用于实施本发明方法的蛋白质阵列装置和试剂盒。

    Assessing rheumatoid arthritis by measuring anti-CCP and interleukin 6
    8.
    发明授权
    Assessing rheumatoid arthritis by measuring anti-CCP and interleukin 6 有权
    通过测量抗CCP和白细胞介素6评估类风湿关节炎

    公开(公告)号:US07846674B2

    公开(公告)日:2010-12-07

    申请号:US11472069

    申请日:2006-06-21

    IPC分类号: G01N33/53

    CPC分类号: G01N33/564 G01N33/6869

    摘要: The present invention relates to a method aiding in the assessment of rheumatoid arthritis. The method especially is used in assessing the absence or presence of rheumatoid arthritis in vitro. The method is for example practiced by analyzing biochemical markers, comprising measuring in a sample the concentration of anti-CCP and interleukin 6 and correlating the concentrations determined to the absence or presence of rheumatoid arthritis. To further improve the assessment of RA in a method of this invention the level of one or more additional marker may be determined together with anti-CCP and interleukin 6 and be correlated to the absence or presence of RA. The invention also relates to the use of a marker panel comprising anti-CCP and interleukin 6 in the diagnosis of rheumatoid arthritis and it teaches a kit for performing the method of the invention.

    摘要翻译: 本发明涉及一种协助评估类风湿性关节炎的方法。 该方法特别用于评估体外不存在或存在类风湿性关节炎。 该方法例如通过分析生物化学标记实施,包括在样品中测量抗CCP和白细胞介素6的浓度,并将确定的浓度与不存在或存在类风湿性关节炎相关联。 为了进一步改善本发明方法中RA的评估,可以与抗CCP和白细胞介素6一起测定一种或多种另外的标记物的水平,并与RA的不存在或存在相关。 本发明还涉及包含抗CCP和白介素6的标记物在诊断类风湿性关节炎中的用途,并且其教导了用于实施本发明方法的试剂盒。

    Method to assess the severity of rheumatoid arthritis by measuring anti-CCP and serum amyloid A
    10.
    发明授权
    Method to assess the severity of rheumatoid arthritis by measuring anti-CCP and serum amyloid A 有权
    通过测量抗CCP和血清淀粉样蛋白A评估类风湿关节炎的严重程度的方法

    公开(公告)号:US08062907B2

    公开(公告)日:2011-11-22

    申请号:US13024543

    申请日:2011-02-10

    摘要: Disclosed is a method for assessing a severity of rheumatoid arthritis. The method involves measuring in a patient sample a concentration of anti-cyclic citrullinated peptides (anti-CCP) and serum amyloid A, combining the concentrations determined to obtain a combined value, and comparing the combined value to a cut-off value established from a reference population. In another method, a marker selected from the group consisting of C-reactive protein (CRP), interleukin 6 (IL-6), S100 protein, osteopontin, rheumatoid factor (RF), matrix metalloprotease 1 (MMP-1), matrix metalloprotease 3 (MMP-3), hyaluronic acid, and soluble CD14 (sCD14) may also be determined along with the anti-CCP and serum amyloid A.

    摘要翻译: 公开了一种评估类风湿性关节炎严重程度的方法。 该方法包括在患者样品中测量抗环瓜氨酸肽(抗CCP)和血清淀粉样蛋白A的浓度,将确定的浓度组合以获得组合值,并将组合值与从 参考人口。 在另一种方法中,选自C反应蛋白(CRP),白介素6(IL-6),S100蛋白,骨桥蛋白,类风湿因子(RF),基质金属蛋白酶1(MMP-1),基质金属蛋白酶 3(MMP-3),透明质酸和可溶性CD14(sCD14)也可以与抗CCP和血清淀粉样蛋白A一起测定。