نتایج جستجو برای: cell immortalization

تعداد نتایج: 1684829  

Journal: :Human molecular genetics 1999
Y S Cong J Wen S Bacchetti

Telomerase, the enzyme that synthesizes telomeric DNA, is not expressed in most human somatic cells but is activated with in vitro immortalization and during tumorigenesis, and repressed by cell differentiation. Of the two components of the core enzyme, the catalytic protein hTERT is limiting for activity. To investigate mechanisms of hTERT gene regulation, we have cloned genomic sequences enco...

2006
Sumiyo Endo Paul Nettesheim Mitsuo Oshimura Cheryl Walker

Primary rat trachea! epithelial cells can be transformed in vitro by V methyl-/V'-nitro-/V-nitrosoguanidine. The earliest recognizable morpho logical transformant is the enhanced growth variant (EGV), characterized by enhanced proliferative capacity. Transformed EGV colonies can pro gress to give rise to immortal cell lines. The purpose of this study was to determine if specific chromosome chan...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1988
H Abken C Bützler K Willecke

Transfection of human peripheral blood lymphocytes with DNA from mouse L929 cytoplasts induced proliferation of lymphocytes and the formation of B and T cell-derived cell lines with apparently unlimited growth potential. The cell lines could be grown in serum-containing media as well as in chemically defined serum-free media, have a nearly normal human karyotype, did not form colonies in soft-a...

Journal: :Blood 2005
Yang Du Nancy A Jenkins Neal G Copeland

Retroviruses can induce hematopoietic disease via insertional mutagenesis of cancer genes and provide valuable molecular tags for cancer gene discovery. Here we show that insertional mutagenesis can also identify genes that promote the immortalization of hematopoietic cells, which normally have only limited self-renewal. Transduction of mouse bone marrow cells with replication-incompetent murin...

Journal: :The Malaysian journal of pathology 2007
Lai Meng Looi Min-Hwei Ng Phaik-Leng Cheah

The unique ability of tumour cells to proliferate indefinitely is crucial to neoplastic progression as it allows these cells to express the aggressive properties of cancer without the censure of physiological ageing. This is in contrast to normal somatic cells which are subject to a "mitotic clock," a phenomenon that has been linked to telomeric shortening after each round of cell replication, ...

Journal: :Cancer research 1995
W K Kaufmann E N Levedakou H L Grady R S Paules G H Stein

We have investigated the hypothesis that attenuation of the G2 checkpoint, which delays entry into mitosis in response to damage to DNA and protects against clastogenesis, may contribute to the genetic instability of immortal human cell lines. IMR-90 normal human fibroblasts displayed stringent G2 checkpoint response to gamma-radiation-induced DNA damage. Irradiation with 1.5 Gy induced 98% inh...

2010
Qunfang Li Michael A. Tainsky

The IFN pathway is abrogated in fibroblasts from Li-Fraumeni syndrome (LFS) patients during spontaneous cellular immortalization, a necessary step in carcinogenesis. Microarray profiling of differentially expressed microRNAs (miRNA) revealed that most miRNAs were upregulated in IFN pathway–defective MDAH087-10 fibroblasts compared with MDAH087-N cells with relatively normal IFN signaling. Overe...

2017
Janine Mühe Fred Wang

Epstein-Barr virus (EBV) and related lymphocryptoviruses (LCV) from non-human primates infect B cells, transform their growth to facilitate life-long viral persistence in the host, and contribute to B cell oncogenesis. Co-evolution of LCV with their primate hosts has led to species-specificity so that LCVs preferentially immortalize B cells from their natural host in vitro. We investigated whet...

Journal: :Cell cycle 2008
Hideki Harada Hiroshi Nakagawa Munenori Takaoka James Lee Meenhard Herlyn J Alan Diehl Anil K Rustgi

In eukaryotic cells, MCM, the minichromosome maintenance proteins, form a heterohexamer during G(1) phase in the cell cycle and constitute a DNA helicase activity at the onset of replication. MCM proteins are downregulated and dissociated from chromatin when cells exit the cell cycle. MCM proteins are upregulated frequently in a variety of dysplastic and cancer cells. To delineate the role of M...

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