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    • 42. 发明申请
    • Diagnosis of cancer or benign tumor using the aberrant expression product of the klk4 gene
    • 使用klk4基因的异常表达产物诊断癌症或良性肿瘤
    • US20040137455A1
    • 2004-07-15
    • US10473485
    • 2004-03-15
    • Ying DongJudith Ann Clements
    • C12Q001/68G01N033/574
    • C12N9/6445A61K38/1709C07K16/40G01N33/57434G01N33/57442G01N33/57449G01N33/57496
    • The present invention discloses aberrant expression products of the KLK4 gene, which segregate with at least one condition selected from a cancer or a benign tumour. The invention also discloses a method for detecting the presence or diagnosing the risk of said at least one condition by detecting aberrant KLK4 expression The invention also discloses isolated polynucleotides comprising a nucleotide sequence that corresponds or is complementary to at least a portion of an aberrant KLK4 polynucleotide, which correlates with the presence or risk of said at least one condition. Also disclosed are isolated polypeptides comprising an amino acid sequence that corresponds to at least a portion of an aberrant K4 polypeptide, which correlates with the presence or risk of said at least one condition. The invention also extends to variants and derivatives of these molecules, to vectors comprising aberrant KLK4 polynucleotides and to host cells containing such vectors. The invention further extends to antigen-binding molecules that are immuno-interactive with aberrant K4 polypeptides and to the use of these antigen-binding molecules, the aberrant KLK4 polynucleotides and aberrant K4 polypeptides in assays and kits for detecting the presence or diagnosing the risk of said at least one condition. The invention further encompasses the use of functional KLK4 polynucleotides or functional K4 polypeptides or agents that modulate the level and/or functional activity of an expression product of KLK4 or of a gene belonging to the same biosynthetic or regulatory pathway as KLK4 for treating and/or preventing one or more of said conditions.
    • 本发明公开了KLK4基因的异常表达产物,其与至少一种选自癌症或良性肿瘤的病症分离。 本发明还公开了通过检测异常KLK4表达来检测存在或诊断所述至少一种病症的风险的方法。本发明还公开了分离的多核苷酸,其包含与异常KLK4多核苷酸的至少一部分相对应或互补的核苷酸序列 ,其与所述至少一个条件的存在或风险相关。 还公开了分离的多肽,其包含对应于异常K4多肽的至少一部分的氨基酸序列,其与所述至少一种病症的存在或风险相关。 本发明还延伸到这些分子的变体和衍生物,包含异常KLK4多核苷酸的载体和含有这些载体的宿主细胞。 本发明进一步扩展到与异常K4多肽免疫相互作用的抗原结合分子以及这些抗原结合分子,异常KLK4多核苷酸和异常K4多肽在测定和试剂盒中的用途,用于检测其存在或诊断风险 说至少有一个条件。 本发明还包括使用功能性KLK4多核苷酸或功能性K4多肽或调节KLK4或属于与KLK4相同的生物合成或调节途径的基因的表达产物的水平和/或功能活性的药剂,用于治疗和/或 防止一种或多种所述条件。
    • 43. 发明申请
    • Tumor homing molecules, conjugates derived therefrom, and methods of using same
    • 肿瘤归巢分子,衍生自其的共轭物及其使用方法
    • US20040131623A9
    • 2004-07-08
    • US10375992
    • 2003-02-27
    • THE BURNHAM INSTITUTE
    • Erkki RuoslahtiRenata Pasqualini
    • G01N033/574A61K039/395
    • G01N33/5011A61K47/64G01N33/57492G01N2333/70546G01N2333/948
    • The present invention provides tumor homing molecules, which selectively home to a tumor. The invention also provides methods of using a tumor homing molecule to target an agent such as a drug to a selected tumor or to identify the target molecule expressed by the tumor. The invention also provides methods of targeting a tumor containing angiogenic vasculature by contacting the tumor with a molecule that specifically binds an nullv-containing integrin. The invention further provides molecules that can selectively home to angiogenic vasculature. In addition, the invention provides a target molecule, which is specifically bound by a tumor homing molecule and is expressed by angiogenic vasculature. The invention also provides antibodies that bind to the target molecule and peptidomimetics that competitively inhibit binding of a ligand to the target molecule.
    • 本发明提供了肿瘤归巢分子,其选择性地归巢于肿瘤。 本发明还提供使用肿瘤归巢分子将药物如药物靶向所选择的肿瘤或鉴定由肿瘤表达的靶分子的方法。 本发明还提供了通过使肿瘤与特异性结合含alphav的整联蛋白的分子接触来靶向含有血管生成脉管系统的肿瘤的方法。 本发明进一步提供可以选择性地归属于血管生成脉管系统的分子。 此外,本发明提供了靶分子,其特异性地被肿瘤归巢分子结合并且由血管生成脉管系统表达。 本发明还提供了结合靶分子的抗体和竞争性抑制配体与靶分子结合的肽模拟物。
    • 47. 发明申请
    • Method of screening agents for the treatment and prevention of cancer and cachexia and the new use of specific agents for the treatment and prevention of cancer and cachexia
    • 用于治疗和预防癌症和恶病质的筛选剂的方法以及用于治疗和预防癌症和恶病质的特定药剂的新用途
    • US20040115708A1
    • 2004-06-17
    • US10665221
    • 2003-09-17
    • C. Murray Ardies
    • C12Q001/68G01N033/574
    • C12Q1/6883C12Q1/6886C12Q2600/136G01N33/5011
    • A method for screening agents to determine possible use as treatment and prevention drugs is provided. More specifically, cells, living organisms, mammals, or tissue are treated with the compound or agent of interest and then measured for transient activation of stress-response pathways. Activation of any of the genes or signaling molecules associated with a stress-response pathway is then determined. A transient activation of any of the genes within these pathways of transcription activation indicates the agent is a candidate for a drug, or a source of a drug for the treatment and prevention of cachexia, other wasting disorders, cancer, atherosclerosis, heart disease, autoimmune disease, chronic inflammatory disease, alcoholic hepatitis, non-alcoholic hepatitis, rheumatoid arthritis, osteoarthritis, type II diabetes, insulin insensitivity, Parkinson's disease, Alzheimer's disease, and any other condition caused or mediated by chronic oxygen radical damage or by chronic chemical toxicities. Methods of treatment and uses of specific agents are also provided.
    • 提供了筛选试剂以确定作为治疗和预防药物的可能用途的方法。 更具体地,用感兴趣的化合物或药剂处理细胞,活生物体,哺乳动物或组织,然后测量应激反应途径的瞬时活化。 然后确定与应激反应途径相关联的任何基因或信号分子的活化。 这些转录激活途径中任何基因的瞬时激活表明该药物是药物的候选物,或用于治疗和预防恶病质,其它消耗疾病,癌症,动脉粥样硬化,心脏病,自身免疫的药物的来源 疾病,慢性炎性疾病,酒精性肝炎,非酒精性肝炎,类风湿性关节炎,骨关节炎,II型糖尿病,胰岛素不敏感,帕金森病,阿尔茨海默病以及由慢性氧自由基损伤或慢性化学毒性引起或介导的任何其他病症。 还提供了治疗和使用特定药剂的方法。
    • 50. 发明申请
    • Monoclonal antibody against estrogen stimulated leucine aminopeptidase
    • 针对雌激素刺激的亮氨酸氨基肽酶的单克隆抗体
    • US20040106143A1
    • 2004-06-03
    • US10705991
    • 2003-11-12
    • Gabriel Pulido-Cejudo
    • C12Q001/68G01N033/574
    • G01N33/56988A61K38/4813A61K39/395A61K2039/505C07K16/3015C07K16/40C12Q1/37G01N33/573G01N33/57415Y10S435/975A61K2300/00
    • The identification and characterization of risk factors and their molecular implications in the pathophysiology of human diseases such as cancer is essential for designing efficient diagnostic assays and therapeutic compounds. Estrogenic steroids, under normal physiological conditions, have been shown to play a critical function in several tissues. The response of such a variety of tissues to estrogen stimulation can explain in part its active role in the development and progression of different human diseases, particularly Breast Cancer. Searching for estrogen-responding cellular factors in parental cells of primary human breast carcinomas obtained from tumour biopsies an isoenzyme of putative Leucine Aminopeptidase (LAPase; EC 3.4.11.1) was identified. Results have demonstrated that this marker is found to be elevated in the sera of women with invasive ductal and metastatic carcinomas. A monoclonal antibody against this cellular marker have been produced. This invention refers to the use of LAPase monoclonal antibodies for first line confirmatory blood-based testing for Breast Cancer.
    • 识别和表征危险因素及其在人类疾病如癌症的病理生理学中的分子意义对于设计有效的诊断测定和治疗化合物至关重要。 在正常生理条件下,雌激素类固醇已显示在几种组织中起关键作用。 这种多种组织对雌激素刺激的反应可以部分解释其在不同人类疾病,特别是乳腺癌的发展和进展中的积极作用。 在从肿瘤活检中获得的原代人乳腺癌的亲代细胞中寻找雌激素反应性细胞因子,鉴定出推定的亮氨酸氨基肽酶(LAPase; EC 3.4.11.1)的同工酶。 结果表明,这种标志物被发现在具有浸润性导管和转移性癌症的妇女的血清中升高。 已经产生了针对该细胞标记物的单克隆抗体。 本发明涉及使用LAPase单克隆抗体进行乳腺癌一线验证性血液检测。