Topoisomerase I protein expression in primary colorectal cancer and lymph node metastases

A. Boonsong, Stephanie Curran, J. A. McKay, J. Cassidy, Graeme Ian Murray, H. L. McLeod

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Topoisomerase I (topo I) is an important target for the treatment of malignant disease, especially colorectal cancer. Because there is little information on the expression of topo I in colorectal tumors, this study evaluated and characterized topo I protein expression in primary colorectal cancer and lymph node metastases and studied the association between topo I protein expression and clinicopathologic data, p53 status, and proliferating cell nuclear antigen (PCNA) status. Immunohistochemistry assay was performed for topo I protein expression in 249 primary human colorectal cancer and 42 paired lymph node metastasis samples. Topo I expression was described as the percentage of cells staining positive for topo I, along with the intensity and localization of the staining. Clinicopathologic data (sex, age, Dukes' stage, differentiation grade, survival status), p53 status, and PCNA status were statistically analyzed for association with topo I protein expression. Topo I expression in paired primary lymph node metastases were studied for concordance. Topo I protein expression was detected in 127 (51%) samples, including 24.4% with >50% positive tumor cells. The majority had nuclear (70.1%) or nuclear and cytoplasmic staining (17.3%). A higher percentage of cells expressing topo I in primary colorectal cancer was significantly associated with advanced age (P =.040). Patients with rectal cancer had greater topo I expression than those with colon tumors (P =.029). No significant correlation was found between topo I protein expression and sex, Dukes' stage, differentiation grade, survival status, p53 status, and PCNA status. Concordance in topo I staining between primary and lymph node metastases was observed in 33 of 42 cases (P =.029). This suggests that the activity of topo I inhibitors will not differ across various tumor stages, pathology, and patient gender. p53 and PCNA status do not appear to influence topo I expression, and topo I has no apparent association with the acquisition of a metastatic phenotype. Topo I expression now needs to be evaluated in patients undergoing topo I-inhibitor therapy, to better define the role of this protein as a predictive marker. HUM PATHOL 33:1114-1119. Copyright 2002, Elsevier Science (USA). All rights reserved.

Original languageEnglish
Pages (from-to)1114-1119
Number of pages5
JournalHuman Pathology
Volume33
Issue number11
DOIs
Publication statusPublished - 2002

Keywords

  • topoisomerase I
  • colorectal cancer
  • immunohistochemistry
  • HUMAN-COLON-CANCER
  • CELL-LINES
  • CATALYTIC ACTIVITY
  • ALPHA
  • P53
  • CAMPTOTHECIN
  • SENSITIVITY
  • MECHANISM
  • CARCINOMA
  • PROLIFERATION

Cite this

Topoisomerase I protein expression in primary colorectal cancer and lymph node metastases. / Boonsong, A.; Curran, Stephanie; McKay, J. A.; Cassidy, J.; Murray, Graeme Ian; McLeod, H. L.

In: Human Pathology, Vol. 33, No. 11, 2002, p. 1114-1119.

Research output: Contribution to journalArticle

Boonsong, A. ; Curran, Stephanie ; McKay, J. A. ; Cassidy, J. ; Murray, Graeme Ian ; McLeod, H. L. / Topoisomerase I protein expression in primary colorectal cancer and lymph node metastases. In: Human Pathology. 2002 ; Vol. 33, No. 11. pp. 1114-1119.
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AU - Murray, Graeme Ian

AU - McLeod, H. L.

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N2 - Topoisomerase I (topo I) is an important target for the treatment of malignant disease, especially colorectal cancer. Because there is little information on the expression of topo I in colorectal tumors, this study evaluated and characterized topo I protein expression in primary colorectal cancer and lymph node metastases and studied the association between topo I protein expression and clinicopathologic data, p53 status, and proliferating cell nuclear antigen (PCNA) status. Immunohistochemistry assay was performed for topo I protein expression in 249 primary human colorectal cancer and 42 paired lymph node metastasis samples. Topo I expression was described as the percentage of cells staining positive for topo I, along with the intensity and localization of the staining. Clinicopathologic data (sex, age, Dukes' stage, differentiation grade, survival status), p53 status, and PCNA status were statistically analyzed for association with topo I protein expression. Topo I expression in paired primary lymph node metastases were studied for concordance. Topo I protein expression was detected in 127 (51%) samples, including 24.4% with >50% positive tumor cells. The majority had nuclear (70.1%) or nuclear and cytoplasmic staining (17.3%). A higher percentage of cells expressing topo I in primary colorectal cancer was significantly associated with advanced age (P =.040). Patients with rectal cancer had greater topo I expression than those with colon tumors (P =.029). No significant correlation was found between topo I protein expression and sex, Dukes' stage, differentiation grade, survival status, p53 status, and PCNA status. Concordance in topo I staining between primary and lymph node metastases was observed in 33 of 42 cases (P =.029). This suggests that the activity of topo I inhibitors will not differ across various tumor stages, pathology, and patient gender. p53 and PCNA status do not appear to influence topo I expression, and topo I has no apparent association with the acquisition of a metastatic phenotype. Topo I expression now needs to be evaluated in patients undergoing topo I-inhibitor therapy, to better define the role of this protein as a predictive marker. HUM PATHOL 33:1114-1119. Copyright 2002, Elsevier Science (USA). All rights reserved.

AB - Topoisomerase I (topo I) is an important target for the treatment of malignant disease, especially colorectal cancer. Because there is little information on the expression of topo I in colorectal tumors, this study evaluated and characterized topo I protein expression in primary colorectal cancer and lymph node metastases and studied the association between topo I protein expression and clinicopathologic data, p53 status, and proliferating cell nuclear antigen (PCNA) status. Immunohistochemistry assay was performed for topo I protein expression in 249 primary human colorectal cancer and 42 paired lymph node metastasis samples. Topo I expression was described as the percentage of cells staining positive for topo I, along with the intensity and localization of the staining. Clinicopathologic data (sex, age, Dukes' stage, differentiation grade, survival status), p53 status, and PCNA status were statistically analyzed for association with topo I protein expression. Topo I expression in paired primary lymph node metastases were studied for concordance. Topo I protein expression was detected in 127 (51%) samples, including 24.4% with >50% positive tumor cells. The majority had nuclear (70.1%) or nuclear and cytoplasmic staining (17.3%). A higher percentage of cells expressing topo I in primary colorectal cancer was significantly associated with advanced age (P =.040). Patients with rectal cancer had greater topo I expression than those with colon tumors (P =.029). No significant correlation was found between topo I protein expression and sex, Dukes' stage, differentiation grade, survival status, p53 status, and PCNA status. Concordance in topo I staining between primary and lymph node metastases was observed in 33 of 42 cases (P =.029). This suggests that the activity of topo I inhibitors will not differ across various tumor stages, pathology, and patient gender. p53 and PCNA status do not appear to influence topo I expression, and topo I has no apparent association with the acquisition of a metastatic phenotype. Topo I expression now needs to be evaluated in patients undergoing topo I-inhibitor therapy, to better define the role of this protein as a predictive marker. HUM PATHOL 33:1114-1119. Copyright 2002, Elsevier Science (USA). All rights reserved.

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KW - immunohistochemistry

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KW - CELL-LINES

KW - CATALYTIC ACTIVITY

KW - ALPHA

KW - P53

KW - CAMPTOTHECIN

KW - SENSITIVITY

KW - MECHANISM

KW - CARCINOMA

KW - PROLIFERATION

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JO - Human Pathology

JF - Human Pathology

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