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Ki-ras point mutations and proliferation activity in biliary tract carcinomas.

The association between Ki-ras mutations and proliferation activity was investigated in a comprehensive series of biliary tract carcinomas (BTCs). We precisely microdissected samples of tissue from paraffin-embedded sections of 77 BTCs including 22 intrahepatic cholangiocarcinomas (ICCs), 36 extrahe...

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Autores principales: Ohashi, K., Tstsumi, M., Nakajima, Y., Nakano, H., Konishi, Y.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074747/
https://www.ncbi.nlm.nih.gov/pubmed/8826860
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author Ohashi, K.
Tstsumi, M.
Nakajima, Y.
Nakano, H.
Konishi, Y.
author_facet Ohashi, K.
Tstsumi, M.
Nakajima, Y.
Nakano, H.
Konishi, Y.
author_sort Ohashi, K.
collection PubMed
description The association between Ki-ras mutations and proliferation activity was investigated in a comprehensive series of biliary tract carcinomas (BTCs). We precisely microdissected samples of tissue from paraffin-embedded sections of 77 BTCs including 22 intrahepatic cholangiocarcinomas (ICCs), 36 extrahepatic cholangiocarcinomas (ECCs), and 19 gall bladder carcinomas (GBCs). Ki-ras mutations at exons 1 and 2 were determined by the polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) method and confirmed by direct sequencing. Proliferation activity was immunohistochemically assessed to generate proliferating cell nuclear antigen labelling indices (PCNA LIs). Ki-ras mutations were detected in 10 of 22 ICCs (45%), 24 of 36 ECCs (67%), and in 16 of 19 GBCs (84%). The frequency of Ki-ras mutations in peripheral type ICCs was 33% (4 of 12) and that in the hilar type ICCs was 60% (6 of 10). In ECCs the highest value of 82% (9 of 11) was found for carcinomas located in the lower part of the biliary tree. Mean PCNA LI in mutation-positive BTCs was significantly elevated compared with the mutation-negative value. These results indicate frequent involvement of Ki-ras mutations in BTCs, especially in GBCs and in distal ECCs, and that carcinomas harbouring a mutation feature high cell proliferation activity. IMAGES:
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spelling pubmed-20747472009-09-10 Ki-ras point mutations and proliferation activity in biliary tract carcinomas. Ohashi, K. Tstsumi, M. Nakajima, Y. Nakano, H. Konishi, Y. Br J Cancer Research Article The association between Ki-ras mutations and proliferation activity was investigated in a comprehensive series of biliary tract carcinomas (BTCs). We precisely microdissected samples of tissue from paraffin-embedded sections of 77 BTCs including 22 intrahepatic cholangiocarcinomas (ICCs), 36 extrahepatic cholangiocarcinomas (ECCs), and 19 gall bladder carcinomas (GBCs). Ki-ras mutations at exons 1 and 2 were determined by the polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) method and confirmed by direct sequencing. Proliferation activity was immunohistochemically assessed to generate proliferating cell nuclear antigen labelling indices (PCNA LIs). Ki-ras mutations were detected in 10 of 22 ICCs (45%), 24 of 36 ECCs (67%), and in 16 of 19 GBCs (84%). The frequency of Ki-ras mutations in peripheral type ICCs was 33% (4 of 12) and that in the hilar type ICCs was 60% (6 of 10). In ECCs the highest value of 82% (9 of 11) was found for carcinomas located in the lower part of the biliary tree. Mean PCNA LI in mutation-positive BTCs was significantly elevated compared with the mutation-negative value. These results indicate frequent involvement of Ki-ras mutations in BTCs, especially in GBCs and in distal ECCs, and that carcinomas harbouring a mutation feature high cell proliferation activity. IMAGES: Nature Publishing Group 1996-09 /pmc/articles/PMC2074747/ /pubmed/8826860 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Ohashi, K.
Tstsumi, M.
Nakajima, Y.
Nakano, H.
Konishi, Y.
Ki-ras point mutations and proliferation activity in biliary tract carcinomas.
title Ki-ras point mutations and proliferation activity in biliary tract carcinomas.
title_full Ki-ras point mutations and proliferation activity in biliary tract carcinomas.
title_fullStr Ki-ras point mutations and proliferation activity in biliary tract carcinomas.
title_full_unstemmed Ki-ras point mutations and proliferation activity in biliary tract carcinomas.
title_short Ki-ras point mutations and proliferation activity in biliary tract carcinomas.
title_sort ki-ras point mutations and proliferation activity in biliary tract carcinomas.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074747/
https://www.ncbi.nlm.nih.gov/pubmed/8826860
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