Differences in the expression of glutathione S-transferases in normal pancreas, chronic pancreatitis, secondary chronic pancreatitis, and pancreatic cancer

Alexis B. Ulrich, Bruno M. Schmied, Jens Standop, Matthias B. Schneider, Terence A Lawson, Helmut Friess, Åke Andrén-Sandberg, Markus W. Büchler, Parviz M. Pour

Research output: Contribution to journalArticle

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Abstract

Introduction: In our previous study, glutathione S-trasferase-π (GST-π), a phase II drug metabolizing enzyme, was found to be expressed in pancreatic ductal and ductular cells but not acinar cells of the normal pancreas, chronic pancreatitis, and secondary pancreatitis caused by pancreatic cancer. A greater percentage of the cells expressing GST-π was shown in the islets of chronic pancreatitis specimens compared with the normal pancreas and secondary pancreatitis. Aims and Methodology: To examine whether the increased number of islet cells expressing GST-π and the absence in the acinar cells are compensated for by other GST isozymes, we investigated the expression of GST-α and GST-μ in the same specimens. Results: Unlike the distribution of GST-π, the distribution of GST-α and GST-μ in islets did not show marked differences between the three groups. However, in four of 18 primary chronic pancreatitis specimens, more islet cells (approximately 25%) expressed GST-α than in the normal pancreas and secondary chronic pancreatitis (both approximately 10%). The reactivity of cancer cells to GST-α, GST-μ, and GST-π was similar to the ductal cells in the normal pancreas, chronic pancreatitis, and secondary chronic pancreatitis. Contrary to the expression of GST-π, no statistically significant differences were found in the distribution of GST-α and GST-μ in the normal pancreas, chronic pancreatitis, and secondary chronic pancreatitis. Conclusion: The expression of the other GSTs does not compensate for the variation of expression of GST-π. There was no specimen in each group that did not express at least one GST isozyme in islet, acinar, and ductal cells.

Original languageEnglish (US)
Pages (from-to)291-297
Number of pages7
JournalPancreas
Volume24
Issue number3
DOIs
StatePublished - Apr 9 2002

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Chronic Pancreatitis
Glutathione Transferase
Pancreatic Neoplasms
Glutathione
Pancreas
Acinar Cells
Islets of Langerhans
Pancreatitis
Isoenzymes

Keywords

  • Chronic pancreatitis
  • Glutathione S-transferases
  • Immunohistochemistry
  • Islets
  • Normal pancreas
  • Pancreatic cancer

ASJC Scopus subject areas

  • Internal Medicine
  • Endocrinology, Diabetes and Metabolism
  • Hepatology
  • Endocrinology

Cite this

Differences in the expression of glutathione S-transferases in normal pancreas, chronic pancreatitis, secondary chronic pancreatitis, and pancreatic cancer. / Ulrich, Alexis B.; Schmied, Bruno M.; Standop, Jens; Schneider, Matthias B.; Lawson, Terence A; Friess, Helmut; Andrén-Sandberg, Åke; Büchler, Markus W.; Pour, Parviz M.

In: Pancreas, Vol. 24, No. 3, 09.04.2002, p. 291-297.

Research output: Contribution to journalArticle

Ulrich, AB, Schmied, BM, Standop, J, Schneider, MB, Lawson, TA, Friess, H, Andrén-Sandberg, Å, Büchler, MW & Pour, PM 2002, 'Differences in the expression of glutathione S-transferases in normal pancreas, chronic pancreatitis, secondary chronic pancreatitis, and pancreatic cancer', Pancreas, vol. 24, no. 3, pp. 291-297. https://doi.org/10.1097/00006676-200204000-00013
Ulrich, Alexis B. ; Schmied, Bruno M. ; Standop, Jens ; Schneider, Matthias B. ; Lawson, Terence A ; Friess, Helmut ; Andrén-Sandberg, Åke ; Büchler, Markus W. ; Pour, Parviz M. / Differences in the expression of glutathione S-transferases in normal pancreas, chronic pancreatitis, secondary chronic pancreatitis, and pancreatic cancer. In: Pancreas. 2002 ; Vol. 24, No. 3. pp. 291-297.
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T1 - Differences in the expression of glutathione S-transferases in normal pancreas, chronic pancreatitis, secondary chronic pancreatitis, and pancreatic cancer

AU - Ulrich, Alexis B.

AU - Schmied, Bruno M.

AU - Standop, Jens

AU - Schneider, Matthias B.

AU - Lawson, Terence A

AU - Friess, Helmut

AU - Andrén-Sandberg, Åke

AU - Büchler, Markus W.

AU - Pour, Parviz M.

PY - 2002/4/9

Y1 - 2002/4/9

N2 - Introduction: In our previous study, glutathione S-trasferase-π (GST-π), a phase II drug metabolizing enzyme, was found to be expressed in pancreatic ductal and ductular cells but not acinar cells of the normal pancreas, chronic pancreatitis, and secondary pancreatitis caused by pancreatic cancer. A greater percentage of the cells expressing GST-π was shown in the islets of chronic pancreatitis specimens compared with the normal pancreas and secondary pancreatitis. Aims and Methodology: To examine whether the increased number of islet cells expressing GST-π and the absence in the acinar cells are compensated for by other GST isozymes, we investigated the expression of GST-α and GST-μ in the same specimens. Results: Unlike the distribution of GST-π, the distribution of GST-α and GST-μ in islets did not show marked differences between the three groups. However, in four of 18 primary chronic pancreatitis specimens, more islet cells (approximately 25%) expressed GST-α than in the normal pancreas and secondary chronic pancreatitis (both approximately 10%). The reactivity of cancer cells to GST-α, GST-μ, and GST-π was similar to the ductal cells in the normal pancreas, chronic pancreatitis, and secondary chronic pancreatitis. Contrary to the expression of GST-π, no statistically significant differences were found in the distribution of GST-α and GST-μ in the normal pancreas, chronic pancreatitis, and secondary chronic pancreatitis. Conclusion: The expression of the other GSTs does not compensate for the variation of expression of GST-π. There was no specimen in each group that did not express at least one GST isozyme in islet, acinar, and ductal cells.

AB - Introduction: In our previous study, glutathione S-trasferase-π (GST-π), a phase II drug metabolizing enzyme, was found to be expressed in pancreatic ductal and ductular cells but not acinar cells of the normal pancreas, chronic pancreatitis, and secondary pancreatitis caused by pancreatic cancer. A greater percentage of the cells expressing GST-π was shown in the islets of chronic pancreatitis specimens compared with the normal pancreas and secondary pancreatitis. Aims and Methodology: To examine whether the increased number of islet cells expressing GST-π and the absence in the acinar cells are compensated for by other GST isozymes, we investigated the expression of GST-α and GST-μ in the same specimens. Results: Unlike the distribution of GST-π, the distribution of GST-α and GST-μ in islets did not show marked differences between the three groups. However, in four of 18 primary chronic pancreatitis specimens, more islet cells (approximately 25%) expressed GST-α than in the normal pancreas and secondary chronic pancreatitis (both approximately 10%). The reactivity of cancer cells to GST-α, GST-μ, and GST-π was similar to the ductal cells in the normal pancreas, chronic pancreatitis, and secondary chronic pancreatitis. Contrary to the expression of GST-π, no statistically significant differences were found in the distribution of GST-α and GST-μ in the normal pancreas, chronic pancreatitis, and secondary chronic pancreatitis. Conclusion: The expression of the other GSTs does not compensate for the variation of expression of GST-π. There was no specimen in each group that did not express at least one GST isozyme in islet, acinar, and ductal cells.

KW - Chronic pancreatitis

KW - Glutathione S-transferases

KW - Immunohistochemistry

KW - Islets

KW - Normal pancreas

KW - Pancreatic cancer

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