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Frequent Genetic Instability in Small Intestinal Carcinomas
To determine whether genetic instability plays a part in the development of digestive tract carcinomas, we analyzed 3 microsatellite loci isolated from tumors and surrounding normal tissue samples obtained during surgery. The polymerase chain reaction (PCR) technique was used to assess differences b...
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Published in: | Cancer science 1995-04, Vol.86 (4), p.357-360 |
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creator | Hibi, Kenji Kondo, Ken Akiyama, Seiji Ito, Katsuki Takagi, Hiroshi |
description | To determine whether genetic instability plays a part in the development of digestive tract carcinomas, we analyzed 3 microsatellite loci isolated from tumors and surrounding normal tissue samples obtained during surgery. The polymerase chain reaction (PCR) technique was used to assess differences between tumor and matched normal DNAs. Replication errors (RERs) were observed in 3 of the 29 cases (10%) of gastric carcinoma and in 11 of the 72 cases (15%) of colorectal carcinoma. None of the 13 (0%) esophageal carcinoma cases showed any RER, but 5 of the 11 cases of small intestinal carcinoma (45%) had RERs, a significantly frequent finding. These results suggest that genetic instability plays an important role in the pathogenesis of small intestinal carcinomas. |
doi_str_mv | 10.1111/j.1349-7006.1995.tb03064.x |
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The polymerase chain reaction (PCR) technique was used to assess differences between tumor and matched normal DNAs. Replication errors (RERs) were observed in 3 of the 29 cases (10%) of gastric carcinoma and in 11 of the 72 cases (15%) of colorectal carcinoma. None of the 13 (0%) esophageal carcinoma cases showed any RER, but 5 of the 11 cases of small intestinal carcinoma (45%) had RERs, a significantly frequent finding. These results suggest that genetic instability plays an important role in the pathogenesis of small intestinal carcinomas.</description><identifier>ISSN: 0910-5050</identifier><identifier>ISSN: 1347-9032</identifier><identifier>EISSN: 1349-7006</identifier><identifier>EISSN: 1876-4673</identifier><identifier>DOI: 10.1111/j.1349-7006.1995.tb03064.x</identifier><identifier>PMID: 7775257</identifier><identifier>CODEN: GANNA2</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Biological and medical sciences ; Colorectal carcinoma ; Colorectal Neoplasms - genetics ; DNA ; DNA Replication - genetics ; DNA, Neoplasm - genetics ; DNA, Satellite - genetics ; Esophageal carcinoma ; Esophagus ; Gastric cancer ; Gastric carcinoma ; Gastroenterology. Liver. Pancreas. Abdomen ; Gastrointestinal tract ; Genetic instability ; Genomic instability ; Hereditary non‐polyposis colorectal cancer ; Humans ; Intestinal Neoplasms - genetics ; Intestine ; Intestine, Small ; man ; Medical sciences ; microsatellites ; Polymerase Chain Reaction ; Small intestinal carcinoma ; small intestine ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Surgery ; Tumors</subject><ispartof>Cancer science, 1995-04, Vol.86 (4), p.357-360</ispartof><rights>1995 INIST-CNRS</rights><rights>Copyright John Wiley & Sons, Inc. 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The polymerase chain reaction (PCR) technique was used to assess differences between tumor and matched normal DNAs. Replication errors (RERs) were observed in 3 of the 29 cases (10%) of gastric carcinoma and in 11 of the 72 cases (15%) of colorectal carcinoma. None of the 13 (0%) esophageal carcinoma cases showed any RER, but 5 of the 11 cases of small intestinal carcinoma (45%) had RERs, a significantly frequent finding. These results suggest that genetic instability plays an important role in the pathogenesis of small intestinal carcinomas.</description><subject>Biological and medical sciences</subject><subject>Colorectal carcinoma</subject><subject>Colorectal Neoplasms - genetics</subject><subject>DNA</subject><subject>DNA Replication - genetics</subject><subject>DNA, Neoplasm - genetics</subject><subject>DNA, Satellite - genetics</subject><subject>Esophageal carcinoma</subject><subject>Esophagus</subject><subject>Gastric cancer</subject><subject>Gastric carcinoma</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Gastrointestinal tract</subject><subject>Genetic instability</subject><subject>Genomic instability</subject><subject>Hereditary non‐polyposis colorectal cancer</subject><subject>Humans</subject><subject>Intestinal Neoplasms - genetics</subject><subject>Intestine</subject><subject>Intestine, Small</subject><subject>man</subject><subject>Medical sciences</subject><subject>microsatellites</subject><subject>Polymerase Chain Reaction</subject><subject>Small intestinal carcinoma</subject><subject>small intestine</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. 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Liver. Pancreas. Abdomen</topic><topic>Gastrointestinal tract</topic><topic>Genetic instability</topic><topic>Genomic instability</topic><topic>Hereditary non‐polyposis colorectal cancer</topic><topic>Humans</topic><topic>Intestinal Neoplasms - genetics</topic><topic>Intestine</topic><topic>Intestine, Small</topic><topic>man</topic><topic>Medical sciences</topic><topic>microsatellites</topic><topic>Polymerase Chain Reaction</topic><topic>Small intestinal carcinoma</topic><topic>small intestine</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. 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The polymerase chain reaction (PCR) technique was used to assess differences between tumor and matched normal DNAs. Replication errors (RERs) were observed in 3 of the 29 cases (10%) of gastric carcinoma and in 11 of the 72 cases (15%) of colorectal carcinoma. None of the 13 (0%) esophageal carcinoma cases showed any RER, but 5 of the 11 cases of small intestinal carcinoma (45%) had RERs, a significantly frequent finding. These results suggest that genetic instability plays an important role in the pathogenesis of small intestinal carcinomas.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>7775257</pmid><doi>10.1111/j.1349-7006.1995.tb03064.x</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biological and medical sciences Colorectal carcinoma Colorectal Neoplasms - genetics DNA DNA Replication - genetics DNA, Neoplasm - genetics DNA, Satellite - genetics Esophageal carcinoma Esophagus Gastric cancer Gastric carcinoma Gastroenterology. Liver. Pancreas. Abdomen Gastrointestinal tract Genetic instability Genomic instability Hereditary non‐polyposis colorectal cancer Humans Intestinal Neoplasms - genetics Intestine Intestine, Small man Medical sciences microsatellites Polymerase Chain Reaction Small intestinal carcinoma small intestine Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Surgery Tumors |
title | Frequent Genetic Instability in Small Intestinal Carcinomas |
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