p53 and behaviour of colorectal cancer
The tumour suppressor gene p53 is altered in most colorectal tumours. We found that lymphatic dissemination was driven by the presence of mutated p53 whether or not the cell contained wild-type p53. In a total sample of 187 specimens, point mutaion of the p53 gene occured in 70% and 43% of cases wit...
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| Veröffentlicht in: | The Lancet (British edition) 1994-07, Vol.344 (8917), p.233-234 |
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| creator | Goh, H-S. Chan, C-S. Khine, K. Smith, D.R. |
| description | The tumour suppressor gene p53 is altered in most colorectal tumours. We found that lymphatic dissemination was driven by the presence of mutated p53 whether or not the cell contained wild-type p53. In a total sample of 187 specimens, point mutaion of the p53 gene occured in 70% and 43% of cases with and without lymph-node involvement, respectively. By contrast, haematogenous dissemination was apparently the result of absent functional wild-type p53 (whether or not the cell contained mutated p53). These results are of potential im-portance in the prediction of the clinical behaviour of a tumour. Lancet 1994;
344: 233–34 |
| doi_str_mv | 10.1016/S0140-6736(94)93000-7 |
| format | Article |
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344: 233–34</description><subject>Biological and medical sciences</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - pathology</subject><subject>DNA, Neoplasm - genetics</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Genes</subject><subject>Genes, p53 - genetics</subject><subject>Humans</subject><subject>Lymphatic Metastasis - genetics</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Mutation</subject><subject>Neoplasm Metastasis - genetics</subject><subject>Ploidies</subject><subject>Point Mutation</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. 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We found that lymphatic dissemination was driven by the presence of mutated p53 whether or not the cell contained wild-type p53. In a total sample of 187 specimens, point mutaion of the p53 gene occured in 70% and 43% of cases with and without lymph-node involvement, respectively. By contrast, haematogenous dissemination was apparently the result of absent functional wild-type p53 (whether or not the cell contained mutated p53). These results are of potential im-portance in the prediction of the clinical behaviour of a tumour. Lancet 1994;
344: 233–34</abstract><cop>London</cop><pub>Elsevier Ltd</pub><pmid>7913159</pmid><doi>10.1016/S0140-6736(94)93000-7</doi><tpages>2</tpages></addata></record> |
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| subjects | Biological and medical sciences Colorectal cancer Colorectal carcinoma Colorectal Neoplasms - genetics Colorectal Neoplasms - pathology DNA, Neoplasm - genetics Gastroenterology. Liver. Pancreas. Abdomen Genes Genes, p53 - genetics Humans Lymphatic Metastasis - genetics Medical research Medical sciences Mutation Neoplasm Metastasis - genetics Ploidies Point Mutation Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumors |
| title | p53 and behaviour of colorectal cancer |
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