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Cancer stem cells in hepatocellular carcinoma - an immunohistochemical study with histopathological association

BACKGROUND & OBJECTIVES: Cancer stem cells (CSCs) may be responsible for tumour recurrence and resistance to chemotherapy in hepatocellular carcinoma (HCC). This study was carried out to evaluate the association between histological parameters and liver CSCs (LCSC) in HCC, and to compare distrib...

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Autores principales: Matthai, Smita Mary, Ramakrishna, Banumathi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683823/
https://www.ncbi.nlm.nih.gov/pubmed/26609030
http://dx.doi.org/10.4103/0971-5916.169195
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author Matthai, Smita Mary
Ramakrishna, Banumathi
author_facet Matthai, Smita Mary
Ramakrishna, Banumathi
author_sort Matthai, Smita Mary
collection PubMed
description BACKGROUND & OBJECTIVES: Cancer stem cells (CSCs) may be responsible for tumour recurrence and resistance to chemotherapy in hepatocellular carcinoma (HCC). This study was carried out to evaluate the association between histological parameters and liver CSCs (LCSC) in HCC, and to compare distribution of liver CSCs in HCC associated with and without hepatitis B virus (HBV) infection. METHODS: Seventy nine tumours (49 surgical resections from 46 patients, and 30 from autopsy) were reviewed. Immunohistochemical staining for the LCSC marker EpCAM (epithelial cell adhesion molecule), liver progenitor cell (LPC) markers CK19 (cytokeratin 19) and neural cell adhesion molecule (NCAM) were performed and were associated with histological features of tumour behaviour. RESULTS: Thirty three tumours (41.8%) showed positive staining for EpCAM. CK19 and NCAM expression were seen in 26 (32.9%) and four (5.1%) tumours, respectively. The expression of EpCAM and CK19 was significantly associated with each other (P<0.001). EpCAM expression was significantly associated with clinical and histological features indicating aggressive tumour behaviour, including younger age of onset, higher serum alpha foetoprotein (AFP) levels, tumour cell dedifferentiation, increased mitotic activity, and vascular invasiveness. There was no significant difference in expression of EpCAM, CK19 and NCAM between HBV positive and negative HCC. INTERPRETATION & CONCLUSIONS: The LCSC marker EpCAM was expressed in less than half of HCC, was independent of HBV aetiology, and was strongly associated with clinical and histological features of aggressive tumour behaviour. Positive staining for CK19 suggests a possible LPC origin of the EpCAM positive HCCs.
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spelling pubmed-46838232015-12-28 Cancer stem cells in hepatocellular carcinoma - an immunohistochemical study with histopathological association Matthai, Smita Mary Ramakrishna, Banumathi Indian J Med Res Original Article BACKGROUND & OBJECTIVES: Cancer stem cells (CSCs) may be responsible for tumour recurrence and resistance to chemotherapy in hepatocellular carcinoma (HCC). This study was carried out to evaluate the association between histological parameters and liver CSCs (LCSC) in HCC, and to compare distribution of liver CSCs in HCC associated with and without hepatitis B virus (HBV) infection. METHODS: Seventy nine tumours (49 surgical resections from 46 patients, and 30 from autopsy) were reviewed. Immunohistochemical staining for the LCSC marker EpCAM (epithelial cell adhesion molecule), liver progenitor cell (LPC) markers CK19 (cytokeratin 19) and neural cell adhesion molecule (NCAM) were performed and were associated with histological features of tumour behaviour. RESULTS: Thirty three tumours (41.8%) showed positive staining for EpCAM. CK19 and NCAM expression were seen in 26 (32.9%) and four (5.1%) tumours, respectively. The expression of EpCAM and CK19 was significantly associated with each other (P<0.001). EpCAM expression was significantly associated with clinical and histological features indicating aggressive tumour behaviour, including younger age of onset, higher serum alpha foetoprotein (AFP) levels, tumour cell dedifferentiation, increased mitotic activity, and vascular invasiveness. There was no significant difference in expression of EpCAM, CK19 and NCAM between HBV positive and negative HCC. INTERPRETATION & CONCLUSIONS: The LCSC marker EpCAM was expressed in less than half of HCC, was independent of HBV aetiology, and was strongly associated with clinical and histological features of aggressive tumour behaviour. Positive staining for CK19 suggests a possible LPC origin of the EpCAM positive HCCs. Medknow Publications & Media Pvt Ltd 2015-10 /pmc/articles/PMC4683823/ /pubmed/26609030 http://dx.doi.org/10.4103/0971-5916.169195 Text en Copyright: © Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution NonCommercial ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Matthai, Smita Mary
Ramakrishna, Banumathi
Cancer stem cells in hepatocellular carcinoma - an immunohistochemical study with histopathological association
title Cancer stem cells in hepatocellular carcinoma - an immunohistochemical study with histopathological association
title_full Cancer stem cells in hepatocellular carcinoma - an immunohistochemical study with histopathological association
title_fullStr Cancer stem cells in hepatocellular carcinoma - an immunohistochemical study with histopathological association
title_full_unstemmed Cancer stem cells in hepatocellular carcinoma - an immunohistochemical study with histopathological association
title_short Cancer stem cells in hepatocellular carcinoma - an immunohistochemical study with histopathological association
title_sort cancer stem cells in hepatocellular carcinoma - an immunohistochemical study with histopathological association
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683823/
https://www.ncbi.nlm.nih.gov/pubmed/26609030
http://dx.doi.org/10.4103/0971-5916.169195
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