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Research Lab Results for carcinoma

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  • Amy Kim Lab

    Principal Investigator:
    Amy K. Kim, M.D.
    Medicine

    The Amy Kim Lab performs basic, translational, and clinical research on liver lesions and hepat...ocellular carcinoma. view more

    Research Areas: Liver lesions, hepatocellular carcinoma
  • James Hamilton Lab

    Principal Investigator:
    James Hamilton, M.D.
    Medicine

    The main research interests of the James Hamilton Lab are the molecular pathogenesis of hepatoc...ellular carcinoma and the development of molecular markers to help diagnose and manage cancer of the liver. In addition, we are investigating biomarkers for early diagnosis, prognosis and response to various treatment modalities. Results of this study will provide a molecular classification of HCC and allow us to identify targets for chemoprevention and treatment. Specifically, we extract genomic DNA and total RNA from liver tissues and use this genetic material for methylation-specific PCR (MSP), cDNA microarray, microRNA microarray and genomic DNA methylation array experiments. view more

    Research Areas: Copper homeostasis, Wilson's disease, cancer, molecular genetics, Early detection biomarker discovery for hepatocellular carcinoma, genomics, pathogenesis, liver injury, liver diseases, regulation of lipid metabolism, hepatocellular carcinoma, Pathogenesis of Liver fibrosis and cancer
  • Liliana Florea Lab

    Principal Investigator:
    Liliana Florea, Ph.D., M.Sc.
    Medicine

    Research in the Liliana Florea Lab applies computational techniques toward modeling and problem... solving in biology and genetic medicine. We work to develop computational methods for analyzing large-scale sequencing data to help characterize molecular mechanisms of diseases. The specific application areas of our research include genome analysis and comparison, cDNA-to-genome alignment, gene and alternative splicing annotation, RNA editing, microbial comparative genomics, miRNA genomics and computational vaccine design. Our most recent studies seek to achieve accurate and efficient RNA-seq correction and explore the role of HCV viral miRNA in hepatocellular carcinoma. view more

    Research Areas: evolutionary genomics, vaccines, carcinoma, cancer, genomics, bioinformatics, RNA, comparative genomics
  • Molecular Genetics Laboratory of Female Reproductive Cancer

    Lab Website
    Principal Investigator:
    Tian-Li Wang, Ph.D.
    Pathology

    The long-term objectives of our research team are:

    a. to understand the molecular etiology ...in the development of human cancer, and
    b. to identify and characterize cancer molecules for cancer detection, diagnosis, and therapy.

    We use ovarian carcinoma as a disease model because it is one of the most aggressive neoplastic diseases in women. For the first research direction, we aim to identify and characterize the molecular alterations during initiation and progression of ovarian carcinomas.
    view more

    Research Areas: genetics, diagnostic pathology, ovarian cancer, gestational trophoblastic diseases
  • Tinsay Woreta

    Principal Investigator:
    Tinsay Woreta, M.D., M.P.H.
    Medicine

    The Woreta Lab does clinical and translational research on Hepatocellular Carcinoma; Liver Tran...splantation Outcomes; Chronic Viral Hepatitis.
    view more

    Research Areas: Chronic Viral Hepatitis, Liver Transplantation Outcomes, hepatocellular carcinoma
  • William G. Nelson Laboratory

    Lab Website
    Principal Investigator:
    William Nelson, M.D., Ph.D.
    Oncology

    Normal and neoplastic cells respond to genome integrity threats in a variety of different ways.... Furthermore, the nature of these responses are critical both for cancer pathogenesis and for cancer treatment. DNA damaging agents activate several signal transduction pathways in damaged cells which trigger cell fate decisions such as proliferation, genomic repair, differentiation, and cell death. For normal cells, failure of a DNA damaging agent (i.e., a carcinogen) to activate processes culminating in DNA repair or in cell death might promote neoplastic transformation. For cancer cells, failure of a DNA damaging agent (i.e., an antineoplastic drug) to promote differentiation or cell death might undermine cancer treatment.

    Our laboratory has discovered the most common known somatic genome alteration in human prostatic carcinoma cells. The DNA lesion, hypermethylation of deoxycytidine nucleotides in the promoter of a carcinogen-defense enzyme gene, appears to result in inactivation of the gene and a resultant increased vulnerability of prostatic cells to carcinogens.
    Studies underway in the laboratory have been directed at characterizing the genomic abnormality further, and at developing methods to restore expression of epigenetically silenced genes and/or to augment expression of other carcinogen-defense enzymes in prostate cells as prostate cancer prevention strategies.

    Another major interest pursued in the laboratory is the role of chronic or recurrent inflammation as a cause of prostate cancer. Genetic studies of familial prostate cancer have identified defects in genes regulating host inflammatory responses to infections.
    A newly described prostate lesion, proliferative inflammatory atrophy (PIA), appears to be an early prostate cancer precursor. Current experimental approaches feature induction of chronic prostate inflammation in laboratory mice and rats, and monitoring the consequences on the development of PIA and prostate cancer.
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    Research Areas: cellular biology, cancer, epigenetics, DNA
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