Abstract:
A bio marker for identifying the exposure of naphthanlene is provided to monitor and determine the contamination of naphthalene through DNA microarray chip. A DNA microarray chip for identifying the exposure of naphthalene comprises oligonucleotide containing whole or part of biomarker gene sequence or its complementary molecule. A method for identifying the exposure of naphthalene comprises: a step of isolating RNA of somatic cell of test sample which is experimental group and somatic cell of control group; a step of synthesizing cDNA and probing with each different fluorescence; a step of hybridizing the cDNA and DNA microarray chip; a step of analyzing the DNA microarray chip; and a step of comparing the expression between control group and experimental group.
Abstract:
A biomarker for identifying the exposure of ethylbenzene and identifying method are provided to determing the monitoring and harmfulness of ethylbenzene using the biomarker. A method for detecting the exposure of ethylbenzene using an biomarker comprises: a step of isolating RNAs from a test sample-derived human somatic cell and somatice cell of control group; a step of synthesizing cDNAs from the experimental group and control group and labeling with different fluorescence; a step of hybridizing with DNA microarray chip; and a step of analyzing DNA microarray chip.
Abstract:
A biomarker for identifying the exposure of trichloroethylene is provided to detect trichloroethylene using genes of which expressions are overexpressed or underexpression by the trichloroethylene. A DNA microarray chip for identifying the exposure to a trichloroethylene is aggregate of a molecule containing oligonulcleotide having entire or a portion of biomarker gene sequence for identifying the exposure of trichloroethylene or its trichloroethylene. A method for identifying the exposure of trichloroethylene comprises: a step of isolating RNAs from human somatic cell isolated from a test sample (experimental group) and somatic cell of control group; a step of synthesizing RNAs to cDNAs and labeling the cDNAs of experimental group and control group; a step of hybridizing the cDNAs on DNA microarray chip; a step of analyzing DNA microarray chip; and a step of comparing the expression. The human somatic cell is derived from bone marrow or cell or tissue of leukemia patient.
Abstract:
A marker gene for screening a drug which induces pulmonary toxicity is provided to monitor and determine a drug or chemical substance causing pulmonary toxicity by increasing or decreasing the expression of the marker by nitofurantoin. An expression of marker gene for screening a drug which causes pulmonary toxicity is increased or decreased by the drug treatment. The drug causing pulmonary toxicity is nitrofurantoin. A DNA microarray chip for screening the drug comprises oligonucleotide containing whole or a part of marker gene sequence or their complement strand. A method for screening the drug comprises: a step of treating a subject compound in a human bronchiolar cell or lung cell; a step of isolating RNA from the subject compound-treated experimental group and untreated-control group; a step of synthesizing cDNA and labeling with each different fluorescence; a step of hybridizing cDNA with DNA microarray; a step of analyzing DNA microarray; and a step of comparing the expressions between the experimental group and control group.
Abstract:
Marker genes for screening drug inducing cardiotoxicity and a screening method thereof are provided to monitor and determine drugs or chemical substances having the risk of heart toxicity by using the reaction genes selected through a DNA microarray chip. A screening method drug inducing cardiotoxicity comprises (1) a step for processing an object compound in HUVEC; (2) a step for separating RNA from the experimental group cell which processes the object compound of the step (1) and the control cell which does not process the object compound; (3) a step for respectively making the experimental group and control group by different fluorescent materials while synthesizing RNA of the experimental group of the step (2) and the control group to cDNA; (4) a step for mixing the cDNA respectively marked by different fluorescent materials of the step (3) with the DNA microarray; (5) a step for analyzing the DNA reacted microarray of the step (4); and (6) a step for comparing and confirming the expressed grade of the marker gene with the control group.
Abstract:
A biomarker is provided to be useful for monitoring methotrexate and determining harmfulness of the methotrexate, thereby being used as a tool for identifying toxicity action mechanism caused by the methotrexate. A biomarker for screening methotrexate includes a gene selected from the group consisting of Genebank NM_004759, Genebank AK122828, Genebank NM_003311, Genebank NM_003506, Genebank NM_005438, Genebank NM_030821, Genebank NM_016205, Genebank AK027210, Genebank NM_018367, Genebank M92424, Genebank NM_000826, Genebank BC036030, Genebank NM_004167, Genebank AB057597, Genebank D26070, Genebank NM_207111, Genebank NM_002511, Genebank NM_000575, Genebank NM_138961, Genebank NM_001024736, Genebank BC002726, Genebank NM_033131, Genebank BC030595, Genebank NM_000710, Genebank AK096323, Genebank NM_078467, Genebank NM_000425, Genebank NM_000899, Genebank NM_002562, Genebank CR594190, Genebank AL832585, Genebank NM_198859, Genebank NM_018667, Genebank NM_001295, Genebank NM_001911, Genebank NM_001759, Genebank NM_000641, Genebank S78234, Genebank AB209361, Genebank BX649005, Genebank AK127679, Genebank AK126462, Genebank NM_003013, Genebank NM_006162, Genebank BC008678, Genebank AK022486, Genebank NM_001315, Genebank BC026283, Genebank AK092791, Genebank BX648822, Genebank BC036078, Genebank L25664, Genebank NM_005419, Genebank CR598645, Genebank NM_031468, Genebank AL833391, Genebank BC033058, Genebank AK127004, Genebank NM_004064, Genebank NM_004360, Genebank BC031405, Genebank BC075814, Genebank M38056, Genebank AB209599, Genebank AY358836, Genebank NM_002758, Genebank NM_006614, Genebank NM_080425, Genebank NM_004526 Genebank L19315, Genebank NM_006120, Genebank NM_002760, Genebank AF041245, Genebank NM_000889, and Genebank AL136787. A total or a portion of the biomarker gene sequence or a complimentary strand molecule thereof is integrated into a DNA microarray chip. A method for screening volatile organic compounds comprises the steps of: (a) treating human bronchial epithelial cells with a compound to be tested; (b) isolating RNA respectively from the test group cells treated with the compound to be tested and control group cells; (c) labelling the test group and the control group, respectively, with a fluorescent material different from each other with synthesizing the RNA of the test group and the control group into cDNA; (d) hybridizing each the cDNA(s) labelled with the fluorescent material into the DNA microarray chip; (e) analyzing the reacted DNA microarray chip; and (f) comparing the expression degree of the biomarker from the data analyzed by the step(e) with that of the control group.
Abstract:
본 발명은 내분비계 장애물질(endocrine disrupting chemicals) 검색용 마커 유전자(marker genes) 및 이를 이용하여 내분비계 장애물질을 검색하는 방법에 관한 것이다. 본 발명의 검색 방법은 마이크로어레이(microarrary)를 통하여 선별된 에스트로겐 반응성 유전자들을 마커(marker)로 이용하여 새로운 내분비계 장애물질을 판정할 수 있으며, 검체의 내분비계 장애물질에 대한 노출 정도를 모니터링 하는데 유용하게 이용할 수 있다.
Abstract:
본 발명은 메틸수은(Methyl mercury) 노출 여부 진단용 바이오마커, 이를 이용하여 MeHg 노출을 진단하는 방법 및 MeHg에 대한 신경세포 보호제에 관한 것으로서, MeHg 노출시 발현 변화를 나타내는 SeW(selenoprotein W) 유전자 또는 단백질을 이용하면 MeHg의 노출 여부 진단에 유용하게 사용될 수 있으며, 글루타치온(GSH)은 MeHg의 독성으로부터 신경세포를 보호하는 신경세포 보호제로 이용될 수 있다. Methyl mercury, neurotoxicity, Selenoprotein W
Abstract:
본 발명은 내분비계 장애물질(endocrine disrupting chemicals) 검색용 마커 유전자(marker genes) 및 이를 이용하여 내분비계 장애물질을 검색하는 방법에 관한 것이다. 본 발명의 검색 방법은 마이크로어레이(microarrary)를 통하여 선별된 에스트로겐 반응성 유전자들을 마커(marker)로 이용하여 새로운 내분비계 장애물질을 판정할 수 있으며, 검체의 내분비계 장애물질에 대한 노출 정도를 모니터링 하는데 유용하게 이용할 수 있다.