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1.
Indian J Cancer ; 2009 Jul-Sept; 46(3): 219-225
Article Dans Anglais | IMSEAR | ID: sea-144242

Résumé

Background and Aim: Colorectal cancer (CRC) is one of the leading malignancies worldwide. CRC has been reported to show geographical variation in its incidence, even within areas of ethnic homogeneity. The aim of this study is to identify K-ras gene mutations in CRC patients among the Kashmiri population, and to assess whether they are linked with the clinicopathological parameters. Materials and Methods: Paired tumor and normal tissue samples were collected from a consecutive series of 53 patients undergoing resective surgery for CRC. In addition blood was also collected from all the cases for ruling out germline mutation. Results: Colorectal patients, 22.64% (12 of 53), presented with mutations in K-ras constituting 13 missense mutations out of which 11 were G→A transition, one G→C transversion, and one G→T transversion. 61.5% percent of the mutations occurred in codon 12 and 38.5% in codon 13. One tumor contained missense mutations in both codons. K-ras mutations were significantly associated with advanced Dukes' stage (P < 0.05) and positive lymph node status (P < 0.05). Moreover Codon 12 K-ras mutations were associated with mucinous histotype (P < 0.05). Comparison of the mutation profile with other high-risk areas reflected both mucinous histotype differences and similarities indicating coexposure to a unique set of risk factors. Conclusion: Mutation of the K-ras gene is one of the commonest genetic changes in the development of human CRC, but it occurs in a rather low frequency in Kashmiri population.


Sujets)
Adénocarcinome/génétique , Adénocarcinome/secondaire , Adulte , Sujet âgé , Tumeurs colorectales/génétique , Tumeurs colorectales/anatomopathologie , ADN tumoral/génétique , Femelle , Gènes ras/génétique , Humains , Inde , Mâle , Adulte d'âge moyen , Mutation/génétique , Réaction de polymérisation en chaîne , Pronostic
2.
Article Dans Anglais | IMSEAR | ID: sea-37368

Résumé

Arsenic, a naturally ocurring chemical element, is considered hazardous to human health. Inorganic arsenic compounds were found to induce cytotoxicity in Chinese hamster V-79 cells in culture. The arsenite form was more toxic than arsenate. Extracts of green and two varieties of black tea, as well as their principal polyphenols, (-)-epigallocatechingallate and theaflavin, efficiently counteracted the cytotoxic effects of arsenic compounds. On the basis of the amount of tea extract that afforded 50% protection to the cells from arsenic induced cytotoxicity, black tea was found to be as effective as green tea. The protective effect was attributable to the contents of not only (-)-epigallocatechingallate but also of theaflavin, the latter being a predominant polyphenol present in black tea.


Sujets)
Animaux , Arsenic/antagonistes et inhibiteurs , Lignée cellulaire tumorale , Chimioprévention , Cricetinae , Cricetulus , Cytotoxines/antagonistes et inhibiteurs , Mâle , Thé
3.
Asian Pac J Allergy Immunol ; 1989 Dec; 7(2): 95-8
Article Dans Anglais | IMSEAR | ID: sea-36947

Résumé

Circulating immune complexes (CICs) in the sera of patients with histologically proven adenocarcinoma of stomach were sequentially studied. Serial CICs levels, quantitated using a sensitive method F(ab')2 anti-C3 ELISA, were measured before surgery and in a post-operative follow up. CICs could be detected in 85% of the patients pre-operatively, while ten days after surgery positivity decreased to 71%. Thirty days after surgery, the mean CIC levels decreased significantly and positivity fell to 46%. The results indicate that removal of primary tumor mass results in a sharp decline of CIC levels.


Sujets)
Adénocarcinome/immunologie , Adulte , Complexe antigène-anticorps/analyse , Test ELISA , Humains , Adulte d'âge moyen , Période postopératoire , Tumeurs de l'estomac/immunologie , Facteurs temps
7.
Indian J Biochem Biophys ; 1980 Feb; 17(1): 12-7
Article Dans Anglais | IMSEAR | ID: sea-28482
11.
Indian J Exp Biol ; 1966 Apr; 4(2): 122-3
Article Dans Anglais | IMSEAR | ID: sea-56202
13.
Indian J Exp Biol ; 1965 Jan; 3(): 64-5
Article Dans Anglais | IMSEAR | ID: sea-59961
14.
Indian J Exp Biol ; 1965 Jan; 3(): 65-6
Article Dans Anglais | IMSEAR | ID: sea-57430
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