Expression of carbonic anhydrase IX in breast is associated with malignant tissues and is related to overexpression of c-erbB2

CA IX is a tumour‐associated carbonic anhydrase with proposed roles in pH modulation and intercellular communication. Its distribution was examined in normal, benign and malignant breast tissues and compared with expression of breast tumour markers including oestrogen receptor, c‐erbB2, c‐erbB3 and...

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Published in:The Journal of pathology Vol. 197; no. 3; pp. 314 - 321
Main Authors: Bartošová, Mária, Parkkila, Seppo, Pohlodek, Kamil, Karttunen, Tuomo J., Galbavý, Štefan, Mucha, Vojtech, Harris, Adrian L., Pastorek, Jaromír, Pastoreková, Silvia
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Published: Chichester, UK John Wiley & Sons, Ltd 01-07-2002
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Abstract CA IX is a tumour‐associated carbonic anhydrase with proposed roles in pH modulation and intercellular communication. Its distribution was examined in normal, benign and malignant breast tissues and compared with expression of breast tumour markers including oestrogen receptor, c‐erbB2, c‐erbB3 and CD44. Tissue specimens were analysed using immunohistochemistry and/or reverse transcriptase–polymerase chain reaction (RT‐PCR). CA IX was detected by IHC in 12/26 (46%) malignant tissues, 4/36 (11%) benign lesions, but not in 10 normal breasts. Staining was mostly confined to plasma membranes of abnormal epithelial cells, but in five cases was found in adjacent stroma. Semi‐quantitative RT‐PCR detected CA9 mRNA in 25/39 (64%) malignant tumours, 11/33 (33%) benign lesions, but in none of three normal breasts. Comparative RT‐PCR analysis of malignant tissues revealed a relationship between CA9 positivity and c‐erbB2 overexpression (p=0.05). Moreover, CA9‐positive specimens displayed a significantly higher median level of c‐erbB2 than CA9‐negative ones (p=0.02). No significant association was found with the other markers. The results of this study support the possible importance of CA IX for breast carcinogenesis and suggest its potential use as a breast tumour marker. Copyright © 2002 John Wiley & Sons, Ltd.
AbstractList CA IX is a tumour‐associated carbonic anhydrase with proposed roles in pH modulation and intercellular communication. Its distribution was examined in normal, benign and malignant breast tissues and compared with expression of breast tumour markers including oestrogen receptor, c‐erbB2, c‐erbB3 and CD44. Tissue specimens were analysed using immunohistochemistry and/or reverse transcriptase–polymerase chain reaction (RT‐PCR). CA IX was detected by IHC in 12/26 (46%) malignant tissues, 4/36 (11%) benign lesions, but not in 10 normal breasts. Staining was mostly confined to plasma membranes of abnormal epithelial cells, but in five cases was found in adjacent stroma. Semi‐quantitative RT‐PCR detected CA9 mRNA in 25/39 (64%) malignant tumours, 11/33 (33%) benign lesions, but in none of three normal breasts. Comparative RT‐PCR analysis of malignant tissues revealed a relationship between CA9 positivity and c‐erbB2 overexpression (p=0.05). Moreover, CA9‐positive specimens displayed a significantly higher median level of c‐erbB2 than CA9‐negative ones (p=0.02). No significant association was found with the other markers. The results of this study support the possible importance of CA IX for breast carcinogenesis and suggest its potential use as a breast tumour marker. Copyright © 2002 John Wiley & Sons, Ltd.
CA IX is a tumour-associated carbonic anhydrase with proposed roles in pH modulation and intercellular communication. Its distribution was examined in normal, benign and malignant breast tissues and compared with expression of breast tumour markers including oestrogen receptor, c-erbB2, c-erbB3 and CD44. Tissue specimens were analysed using immunohistochemistry and/or reverse transcriptase-polymerase chain reaction (RT-PCR). CA IX was detected by IHC in 12/26 (46%) malignant tissues, 4/36 (11%) benign lesions, but not in 10 normal breasts. Staining was mostly confined to plasma membranes of abnormal epithelial cells, but in five cases was found in adjacent stroma. Semi-quantitative RT-PCR detected CA9 mRNA in 25/39 (64%) malignant tumours, 11/33 (33%) benign lesions, but in none of three normal breasts. Comparative RT-PCR analysis of malignant tissues revealed a relationship between CA9 positivity and c-erbB2 overexpression (p=0.05). Moreover, CA9-positive specimens displayed a significantly higher median level of c-erbB2 than CA9-negative ones (p=0.02). No significant association was found with the other markers. The results of this study support the possible importance of CA IX for breast carcinogenesis and suggest its potential use as a breast tumour marker.
CA IX is a tumour‐associated carbonic anhydrase with proposed roles in pH modulation and intercellular communication. Its distribution was examined in normal, benign and malignant breast tissues and compared with expression of breast tumour markers including oestrogen receptor, c‐erbB2, c‐erbB3 and CD44. Tissue specimens were analysed using immunohistochemistry and/or reverse transcriptase–polymerase chain reaction (RT‐PCR). CA IX was detected by IHC in 12/26 (46%) malignant tissues, 4/36 (11%) benign lesions, but not in 10 normal breasts. Staining was mostly confined to plasma membranes of abnormal epithelial cells, but in five cases was found in adjacent stroma. Semi‐quantitative RT‐PCR detected CA9 mRNA in 25/39 (64%) malignant tumours, 11/33 (33%) benign lesions, but in none of three normal breasts. Comparative RT‐PCR analysis of malignant tissues revealed a relationship between CA9 positivity and c‐erb B2 overexpression ( p =0.05). Moreover, CA9 ‐positive specimens displayed a significantly higher median level of c‐erb B2 than CA9 ‐negative ones ( p =0.02). No significant association was found with the other markers. The results of this study support the possible importance of CA IX for breast carcinogenesis and suggest its potential use as a breast tumour marker. Copyright © 2002 John Wiley & Sons, Ltd.
Author Mucha, Vojtech
Pohlodek, Kamil
Karttunen, Tuomo J.
Parkkila, Seppo
Pastorek, Jaromír
Galbavý, Štefan
Harris, Adrian L.
Bartošová, Mária
Pastoreková, Silvia
Author_xml – sequence: 1
  givenname: Mária
  surname: Bartošová
  fullname: Bartošová, Mária
  organization: Department of Molecular Biology, Institute of Virology, Slovak Academy of Sciences, Bratislava, Slovak Republic
– sequence: 2
  givenname: Seppo
  surname: Parkkila
  fullname: Parkkila, Seppo
  organization: Department of Anatomy and Cell Biology, Oulu University, Oulu, Finland
– sequence: 3
  givenname: Kamil
  surname: Pohlodek
  fullname: Pohlodek, Kamil
  organization: Department of Gynaecology and Obstetrics II, School of Medicine, Comenius University, Bratislava, Slovak Republic
– sequence: 4
  givenname: Tuomo J.
  surname: Karttunen
  fullname: Karttunen, Tuomo J.
  organization: Department of Pathology, Oulu University, Oulu, Finland
– sequence: 5
  givenname: Štefan
  surname: Galbavý
  fullname: Galbavý, Štefan
  organization: Department of Pathology, School of Medicine, Comenius University, Bratislava, Slovak Republic
– sequence: 6
  givenname: Vojtech
  surname: Mucha
  fullname: Mucha, Vojtech
  organization: Department of Molecular Biology, Institute of Virology, Slovak Academy of Sciences, Bratislava, Slovak Republic
– sequence: 7
  givenname: Adrian L.
  surname: Harris
  fullname: Harris, Adrian L.
  organization: Molecular Oncology Laboratories, Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, UK
– sequence: 8
  givenname: Jaromír
  surname: Pastorek
  fullname: Pastorek, Jaromír
  organization: Department of Molecular Biology, Institute of Virology, Slovak Academy of Sciences, Bratislava, Slovak Republic
– sequence: 9
  givenname: Silvia
  surname: Pastoreková
  fullname: Pastoreková, Silvia
  email: virupast@savba.sk
  organization: Department of Molecular Biology, Institute of Virology, Slovak Academy of Sciences, Bratislava, Slovak Republic
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IsPeerReviewed true
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Issue 3
Keywords Human
Immunohistochemistry
Carcinoma
Enzyme
Gene overexpression
Lyases
Tumoral marker
Malignant tumor
Gene expression
Carcinogenesis
Polymerase chain reaction
Pathology
Mammary gland diseases
C-Onc gene
Carbonate dehydratase
Mammary gland
Benign neoplasm
Molecular biology
Carbon-oxygen lyases
Protooncogene
Hydro-lyases
Language English
License CC BY 4.0
Copyright 2002 John Wiley & Sons, Ltd.
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According to the carbonic anhydrase nomenclature, human CA isoenzymes are written in capital roman letters and numbers, while their genes are written in italic letters and arabic numbers.
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PublicationTitle The Journal of pathology
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1997; 151
2000; 88
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1999; 46
1997; 28
1996
1999; 86
1999; 83
1999; 81
1991; 314
1998; 153
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1994; 9
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1993; 13
1998; 17
2001; 6
1993; 54
1997; 57
1999; 14
2000; 97
2000; 60
2000; 82
1995; 345
1981
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Liao SY (e_1_2_6_8_2) 1994; 145
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Liao SY (e_1_2_6_28_2) 1997; 57
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World Health Organization (e_1_2_6_22_2) 1981
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Snippet CA IX is a tumour‐associated carbonic anhydrase with proposed roles in pH modulation and intercellular communication. Its distribution was examined in normal,...
CA IX is a tumour-associated carbonic anhydrase with proposed roles in pH modulation and intercellular communication. Its distribution was examined in normal,...
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StartPage 314
SubjectTerms Adult
Aged
Aged, 80 and over
Antigens, Neoplasm
Biological and medical sciences
Biomarkers, Tumor - analysis
Breast - chemistry
breast carcinogenesis
Breast Neoplasms - chemistry
Breast Neoplasms - genetics
c-erbB2
Carbonic Anhydrase IX
Carbonic Anhydrases - analysis
Chi-Square Distribution
Female
Genes, erbB-2
Gynecology. Andrology. Obstetrics
Humans
Hyaluronan Receptors - analysis
Immunohistochemistry
Mammary gland diseases
Medical sciences
Middle Aged
Neoplasm Proteins - analysis
Receptors, Estrogen - analysis
Reverse Transcriptase Polymerase Chain Reaction
semi-quantitative RT-PCR
Tumors
Title Expression of carbonic anhydrase IX in breast is associated with malignant tissues and is related to overexpression of c-erbB2
URI https://api.istex.fr/ark:/67375/WNG-0V6KJJPV-Z/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fpath.1120
https://www.ncbi.nlm.nih.gov/pubmed/12115877
https://search.proquest.com/docview/18461832
Volume 197
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