نتایج جستجو برای: tumor suppressor protein p53

تعداد نتایج: 1594311  

Ardavan Parhizkar Ashraf Mohamadkhani, Ghodratollah Montazeri Hossein Poustchi, Kourosh Sayehmiri, Parisa Shahnazari, Zarrin Minuchehr

Background: The ability of tumour suppressor protein p53 (P53) to regulate cell cycle processes can be modulated by hepatitis B virus (HBV). While preliminary evidences indicates the involvement of protein-x of HBV (HBx) in altering p53 DNA binding, no further data have been accumulated for the significance of serum p53 in chronic hepatitis B virus infected patients. Methods: 72 non-cirrhotic a...

Journal: :Cancer research 2008
Likun Li ElMoataz Abdel Fattah Guangwen Cao Chengzhen Ren Guang Yang Alexei A Goltsov A Craig Chinault Wei-Wen Cai Terry L Timme Timothy C Thompson

Glioma pathogenesis-related protein 1 (GLIPR1), a novel p53 target gene, is down-regulated by methylation in prostate cancer and has p53-dependent and -independent proapoptotic activities in tumor cells. These properties suggest an important tumor suppressor role for GLIPR1, yet direct genetic evidence of a tumor suppressor function for GLIPR1 is lacking and the molecular mechanism(s), through ...

Journal: :The Journal of Experimental Medicine 1997
Michel P.M. Vierboom Hans W. Nijman Rienk Offringa Ellen I.H. van der Voort Thorbald van Hall Lambert van den Broek Gert Jan Fleuren Peter Kenemans W. Martin Kast Cornelis J.M. Melief

The tumor suppressor protein p53 is overexpressed in close to 50% of all human malignancies. The p53 protein is therefore an attractive target for immunotherapy. Cytotoxic T lymphocytes (CTLs) recognizing a murine wild-type p53 peptide, presented by the major histocompatibility complex class I molecule H-2Kb, were generated by immunizing p53 gene deficient (p53 -/-) C57BL/6 mice with syngeneic ...

Journal: :Journal of Biological Chemistry 1997

Journal: :Annals of Oncology 2023

In human colorectal cancer (CRC), TP53 is one of the most important drives genes; it a key regulator apoptosis. The dysfunction gene critical event in development CRC this context, we aimed to evaluate expression Tp53 patients and establish correlation between overexpression p53 with clinical pathological features Colorectal Carcinoma (CRC). This study enrolled 32 carcinoma. was investigated by...

Journal: :The Journal of biological chemistry 1999
M Oren

Mutations in the p53 tumor suppressor gene occur in about 50% of all human tumors, making it the most frequent target for genetic alterations in cancer (for recent reviews on p53 see Refs. 1–5). Such mutations probably facilitate carcinogenesis primarily through abrogating the tumor suppressor activities of the wild type p53 protein, although at least some forms of tumor-associated mutant p53 p...

Journal: :The Journal of biological chemistry 2009
Kamrul Hasan Caroline Cheung Zeenia Kaul Navjot Shah Shinji Sakaushi Kenji Sugimoto Shigenori Oka Sunil C Kaul Renu Wadhwa

The tumor suppressor protein, p53, is central to the pathways that monitor the stress, DNA damage repair, cell cycle, aging, and cancer. Highly complex p53 networks involving its upstream sensors and regulators, downstream effectors and regulatory feedback loops have been identified. CARF (Collaborator of ARF) was shown to enhance ARF-dependent and -independent wild-type p53 function. Here we r...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2002
Gad Asher Joseph Lotem Leo Sachs Chaim Kahana Yosef Shaul

The tumor suppressor p53 is a labile protein whose level is known to be regulated by the Mdm-2-ubiquitin-proteasome degradation pathway. We have found another pathway for p53 proteasomal degradation regulated by NAD(P)H quinone oxidoreductase 1 (NQO1). Inhibition of NQO1 activity by dicoumarol induces p53 and p73 proteasomal degradation. A mutant p53 (p53([22,23])), which is resistant to Mdm-2-...

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