نتایج جستجو برای: tumor suppressor protein p53

تعداد نتایج: 1594311  

Journal: :Cancer research 1996
M C von Brevern M C Hollstein H M Cawley V M De Benedetti W P Bennett L Liang A G He S M Zhu T Tursz N Janin G E Trivers

Serum antibodies reacting with the tumor suppressor protein p53 have been detected previously in cancer patients with a variety of neoplasms. Two initial (although insufficient) prerequisites for a B-cell response to occur have been proposed: p53 protein accumulation in the tumor or a mutant p53 gene, or both. We have examined 65 esophageal cancer cases (42 from Guangzhou and Shenyang, People's...

Journal: :Cancer research 1993
J Yatsunami A Komori T Ohta M Suganuma H Fujiki

A potent tumor promoter, okadaic acid, induced hyperphosphorylation of tumor suppressor proteins, retinoblastoma protein and p53, by in vitro incubation with nuclei isolated from rat regenerating liver as well as by incubation with primary human fibroblasts. Most of the retinoblastoma protein migrated to a hyperphosphorylated position in electrophoresis. The phosphorylation of p53 was increased...

Journal: :Molecular cancer research : MCR 2008
Roberta Malaguarnera Veronica Vella Giuseppe Pandini Mariangela Sanfilippo Vincenzo Pezzino Riccardo Vigneri Francesco Frasca

p53 family proteins include p53 tumor suppressor, p63, and p73. Despite the high similarity in structure and function with p53, p63, and p73 function in tumor suppression is still controversial. Here, we show that TAp73alpha, a transcriptionally active p73 isoform, is able to synergize p53 tumor suppressor function in thyroid cancer cells. Indeed, depletion of p73 by small interfering RNA in th...

2007
Jun Yatsunami Atsumasa Komori Tetsuya Ohta Masami Suganuma

A potent tumor promoter, okadaic acid, induced hyperphosphorylation of tumor suppressor proteins, retinoblastoma protein and p53, by in vitro incubation with nuclei isolated from rat regenerating liver as well as by incubation with primary human fibroblasts. Most of the retinoblastoma protein migrated to a hyperphosphorylated position in electrophoresis. The phosphorylation of p53 was increased...

Journal: :iranian biomedical journal 0
مرضیه حقی شریفیا تقوی marzieh hagi-sharifia taghavi جمشید داوودی jamshid davoodi منوچهر میرشاهی manouchehr mirshahi

the p53 protein function is essential for the maintenance of the nontumorigenic cell phenotype. pancreatic tumor cells show a very high frequency of p53 mutation. to determine if restoration of wild type p53 function can be used to eliminate the tumorigenic phenotype in these cells, pancreatic tumor cell lines, panc-1 and htb80, differing in p53 status were stably transfected with exogenous wil...

Journal: :Cancer research 2003
Yinghui Huang Traci Tyler Neshat Saadatmandi Casey Lee Per Borgstrom Ruth A Gjerset

The p53 tumor suppressor controls a cell cycle arrest and apoptosis pathway that is central to tumor suppression and often disrupted in cancer. The accumulation and activity of p53 are positively controlled by the p14/ARF tumor suppressor and full restoration of the pathway in cancer cells may require that both p53 and p14ARF be supplied [corrected]. To address this issue, we have constructed a...

Azadeh Lohrasbi Nejad Mohammad Mehdi Yaghoobi,

Objective(s) P53 is an important tumor suppressor, which is mutated in later stages of many cancers and leads to resistance to chemotherapy. The aim of this study was to reveal mutations of TP53 in colorectal cancer in Kerman province. Materials and Methods A total of Forty-three colon cancer specimens as paraffin block or fresh tissues, which passed stage IIIA, were selected. Three exons 5,...

2003
Yinghui Huang Traci Tyler Neshat Saadatmandi Casey Lee Per Borgstrom Ruth A. Gjerset Sidney Kimmel

The p53 tumor suppressor controls a cell cycle arrest and apoptosis pathway that is central to tumor suppression and often disrupted in cancer. The accumulation and activity of p53 are positively controlled by the p14 ADP p14ARF ribosylation factor (AR) tumor suppressor, and full restoration of the pathway in cancer cells may require that both p53 and p14ARF be supplied. To address this issue, ...

Journal: :avicenna journal of medical biochemistry 0
satish kumar bioinformatics and biochemistry centre, mahatma gandhi institute of medical sciences, maharashtra university of health sciences, maharashtra, india; bioinformatics and biochemistry centre, mahatma gandhi institute of medical sciences, maharashtra university of health sciences, maharashtra, india. tel: +91-7152284679, fax: +91-7152284038 lingaraja jena bioinformatics and biochemistry centre, mahatma gandhi institute of medical sciences, maharashtra university of health sciences, maharashtra, india maheswata sahoo bioinformatics and biochemistry centre, mahatma gandhi institute of medical sciences, maharashtra university of health sciences, maharashtra, india tapaswini nayak bioinformatics and biochemistry centre, mahatma gandhi institute of medical sciences, maharashtra university of health sciences, maharashtra, india kanchan mohod bioinformatics and biochemistry centre, mahatma gandhi institute of medical sciences, maharashtra university of health sciences, maharashtra, india sangeeta daf datta meghe institute of medical sciences, deemed university, maharashtra, india

materials and methods twelve natural compounds jaceosidin, withaferin a, curcumin, epigallocatechin-3-gallate (egcg), artemisinin, gingerol, ursolic acid, ferulic acid, berberin, silymarin, resveratrol, and indol-3-carbinol were docked against e6 and e7 oncoproteins of high-risk hpv types 16 and 18 using a protein-ligand docking software called autodock4.2. results out of these 12 natural compo...

Jamshid Davoodi, Manouchehr Mirshahi, Marzieh Hagi-Sharifia Taghavi,

The p53 protein function is essential for the maintenance of the nontumorigenic cell phenotype. Pancreatic tumor cells show a very high frequency of p53 mutation. To determine if restoration of wild type p53 function can be used to eliminate the tumorigenic phenotype in these cells, pancreatic tumor cell lines, PANC-1 and HTB80, differing in p53 status were stably transfected with exogenous wil...

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