Differentially regulated ADAMTS1, 8, 9, and 18 in pancreas adenocarcinoma

Introduction : Despite recent diagnostic and therapeutic improvements, pancreas cancer remains one of the highly lethal cancers. The extracellular matrix (ECM) is a physiological barrier that limits the spread of cancer cells into surrounding tissues and distant organs. Disintegrin and metalloprotea...

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Main Authors: Murat Özgür Kılıç, Büşra Aynekin, Mikdat Bozer, Adem Kara, Hacer Haltaş, Duygu İçen, Kadir Demircan
Format: Article
Language:English
Published: Termedia Publishing House 2017-12-01
Series:Gastroenterology Review
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Online Access:https://www.termedia.pl/Differentially-regulated-ADAMTS1-8-9-and-18-in-pancreas-adenocarcinoma,41,31243,1,1.html
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author Murat Özgür Kılıç
Büşra Aynekin
Mikdat Bozer
Adem Kara
Hacer Haltaş
Duygu İçen
Kadir Demircan
author_facet Murat Özgür Kılıç
Büşra Aynekin
Mikdat Bozer
Adem Kara
Hacer Haltaş
Duygu İçen
Kadir Demircan
author_sort Murat Özgür Kılıç
collection DOAJ
description Introduction : Despite recent diagnostic and therapeutic improvements, pancreas cancer remains one of the highly lethal cancers. The extracellular matrix (ECM) is a physiological barrier that limits the spread of cancer cells into surrounding tissues and distant organs. Disintegrin and metalloprotease with thrombospondin motifs (ADAMTS) is a family of 19 proteases, which is involved in various biological processes such as ECM remodelling and anti-angiogenesis. Aim : To investigate the expression of ADAMTS1, 8, 9, and 18 proteinases in pancreas adenocarcinoma and its nodal metastasis. Material and methods : The immunostaining status of ADAMTS1, 8, 9, and 18 were investigated in formalin-fixed paraffin-embedded samples of 25 patients who underwent pancreaticoduodenectomy for an adenocarcinoma located at the head of the pancreas. Results : In semi-quantitive grading pathologically, ADAMTS1, 8, 9, and 18 were found to be highly stained in all cancerous pancreas samples compared with normal pancreas. In addition, the immune positivity of ADAMTS1, 9, and 18 was found to be higher in metastatic lymph nodes than in non-metastatic lymph tissue. Tumour size was correlated with ADAMTS9 and 18 expressions in cancerous pancreas. Conclusions : According to the data obtained from the study, we suggest that these four ADAMTSs may have significant roles in the tumorigenesis and nodal spread of pancreas adenocarcinoma.
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institution Kabale University
issn 1895-5770
1897-4317
language English
publishDate 2017-12-01
publisher Termedia Publishing House
record_format Article
series Gastroenterology Review
spelling doaj-art-23b67b74a0514c8495fe47f223ea7b372025-01-10T14:06:16ZengTermedia Publishing HouseGastroenterology Review1895-57701897-43172017-12-0112426227010.5114/pg.2017.7210131243Differentially regulated ADAMTS1, 8, 9, and 18 in pancreas adenocarcinomaMurat Özgür KılıçBüşra AynekinMikdat BozerAdem KaraHacer HaltaşDuygu İçenKadir DemircanIntroduction : Despite recent diagnostic and therapeutic improvements, pancreas cancer remains one of the highly lethal cancers. The extracellular matrix (ECM) is a physiological barrier that limits the spread of cancer cells into surrounding tissues and distant organs. Disintegrin and metalloprotease with thrombospondin motifs (ADAMTS) is a family of 19 proteases, which is involved in various biological processes such as ECM remodelling and anti-angiogenesis. Aim : To investigate the expression of ADAMTS1, 8, 9, and 18 proteinases in pancreas adenocarcinoma and its nodal metastasis. Material and methods : The immunostaining status of ADAMTS1, 8, 9, and 18 were investigated in formalin-fixed paraffin-embedded samples of 25 patients who underwent pancreaticoduodenectomy for an adenocarcinoma located at the head of the pancreas. Results : In semi-quantitive grading pathologically, ADAMTS1, 8, 9, and 18 were found to be highly stained in all cancerous pancreas samples compared with normal pancreas. In addition, the immune positivity of ADAMTS1, 9, and 18 was found to be higher in metastatic lymph nodes than in non-metastatic lymph tissue. Tumour size was correlated with ADAMTS9 and 18 expressions in cancerous pancreas. Conclusions : According to the data obtained from the study, we suggest that these four ADAMTSs may have significant roles in the tumorigenesis and nodal spread of pancreas adenocarcinoma.https://www.termedia.pl/Differentially-regulated-ADAMTS1-8-9-and-18-in-pancreas-adenocarcinoma,41,31243,1,1.htmlADAMTS immunohistochemistry pancreas cancer
spellingShingle Murat Özgür Kılıç
Büşra Aynekin
Mikdat Bozer
Adem Kara
Hacer Haltaş
Duygu İçen
Kadir Demircan
Differentially regulated ADAMTS1, 8, 9, and 18 in pancreas adenocarcinoma
Gastroenterology Review
ADAMTS
immunohistochemistry
pancreas cancer
title Differentially regulated ADAMTS1, 8, 9, and 18 in pancreas adenocarcinoma
title_full Differentially regulated ADAMTS1, 8, 9, and 18 in pancreas adenocarcinoma
title_fullStr Differentially regulated ADAMTS1, 8, 9, and 18 in pancreas adenocarcinoma
title_full_unstemmed Differentially regulated ADAMTS1, 8, 9, and 18 in pancreas adenocarcinoma
title_short Differentially regulated ADAMTS1, 8, 9, and 18 in pancreas adenocarcinoma
title_sort differentially regulated adamts1 8 9 and 18 in pancreas adenocarcinoma
topic ADAMTS
immunohistochemistry
pancreas cancer
url https://www.termedia.pl/Differentially-regulated-ADAMTS1-8-9-and-18-in-pancreas-adenocarcinoma,41,31243,1,1.html
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AT mikdatbozer differentiallyregulatedadamts189and18inpancreasadenocarcinoma
AT ademkara differentiallyregulatedadamts189and18inpancreasadenocarcinoma
AT hacerhaltas differentiallyregulatedadamts189and18inpancreasadenocarcinoma
AT duyguicen differentiallyregulatedadamts189and18inpancreasadenocarcinoma
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