Protein expression analysis of ALCAM and CEACAM6 in breast cancer metastases reveals significantly increased ALCAM expression in metastases of the skin
AimsFor prediction and understanding of underlying mechanisms of organ-specific metastases, various gene and protein expression signatures have been identified in primary breast carcinomas. These expression signatures often include several genes coding for adhesion molecules, such as activated leuco...
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Published in | Journal of clinical pathology Vol. 64; no. 2; pp. 146 - 152 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BMJ Publishing Group Ltd and Association of Clinical Pathologists
01.02.2011
BMJ Publishing Group BMJ Publishing Group LTD |
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Online Access | Get full text |
ISSN | 0021-9746 1472-4146 1472-4146 |
DOI | 10.1136/jcp.2010.082602 |
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Abstract | AimsFor prediction and understanding of underlying mechanisms of organ-specific metastases, various gene and protein expression signatures have been identified in primary breast carcinomas. These expression signatures often include several genes coding for adhesion molecules, such as activated leucocyte cell adhesion molecule (ALCAM/CD166) and carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6), both of which may play an important role in the development of distant metastases because of their adherent properties. Owing to their predominantly membranous localisation, they are also considered to have certain therapeutic potential. Apart from expression data obtained in the primary tumour, data for gene and protein expression patterns in distant breast cancer metastases are rare. Therefore this study focuses on analysing the distribution of ALCAM and CEACAM6 protein expression in breast cancer metastases from different sites.MethodsImmunohistochemical staining for ALCAM and CEACAM6 in 117 breast cancer metastases derived from liver (n=24), lung (n=19), brain (n=21), bone (n=36) and skin (n=17) was performed.ResultsImmunoreactive scores (IRS) for ALCAM in all metastases except skin metastases ranged from 2.63 to 5.10 (membranous) and 2.79 to 3.67 (cytoplasmic), showing a positive correlation with each other (r=0.690, p<0.001). In skin metastases, ALCAM expression was significantly stronger (membranous IRS, 8.76; cytoplasmic IRS, 7.12; p<0.001). Mean staining intensity for CEACAM6 was IRS 3.88. No or weak CEACAM6 and ALCAM staining (IRS 0–3) was seen in 53% vs 27% of all metastases.ConclusionsCompared with CEACAM6, ALCAM showed significantly stronger protein expression in breast cancer skin metastases compared with metastases in all other sites. |
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AbstractList | For prediction and understanding of underlying mechanisms of organ-specific metastases, various gene and protein expression signatures have been identified in primary breast carcinomas. These expression signatures often include several genes coding for adhesion molecules, such as activated leucocyte cell adhesion molecule (ALCAM/CD166) and carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6), both of which may play an important role in the development of distant metastases because of their adherent properties. Owing to their predominantly membranous localisation, they are also considered to have certain therapeutic potential. Apart from expression data obtained in the primary tumour, data for gene and protein expression patterns in distant breast cancer metastases are rare. Therefore this study focuses on analysing the distribution of ALCAM and CEACAM6 protein expression in breast cancer metastases from different sites.AIMSFor prediction and understanding of underlying mechanisms of organ-specific metastases, various gene and protein expression signatures have been identified in primary breast carcinomas. These expression signatures often include several genes coding for adhesion molecules, such as activated leucocyte cell adhesion molecule (ALCAM/CD166) and carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6), both of which may play an important role in the development of distant metastases because of their adherent properties. Owing to their predominantly membranous localisation, they are also considered to have certain therapeutic potential. Apart from expression data obtained in the primary tumour, data for gene and protein expression patterns in distant breast cancer metastases are rare. Therefore this study focuses on analysing the distribution of ALCAM and CEACAM6 protein expression in breast cancer metastases from different sites.Immunohistochemical staining for ALCAM and CEACAM6 in 117 breast cancer metastases derived from liver (n=24), lung (n=19), brain (n=21), bone (n=36) and skin (n=17) was performed.METHODSImmunohistochemical staining for ALCAM and CEACAM6 in 117 breast cancer metastases derived from liver (n=24), lung (n=19), brain (n=21), bone (n=36) and skin (n=17) was performed.Immunoreactive scores (IRS) for ALCAM in all metastases except skin metastases ranged from 2.63 to 5.10 (membranous) and 2.79 to 3.67 (cytoplasmic), showing a positive correlation with each other (r=0.690, p<0.001). In skin metastases, ALCAM expression was significantly stronger (membranous IRS, 8.76; cytoplasmic IRS, 7.12; p<0.001). Mean staining intensity for CEACAM6 was IRS 3.88. No or weak CEACAM6 and ALCAM staining (IRS 0-3) was seen in 53% vs 27% of all metastases.RESULTSImmunoreactive scores (IRS) for ALCAM in all metastases except skin metastases ranged from 2.63 to 5.10 (membranous) and 2.79 to 3.67 (cytoplasmic), showing a positive correlation with each other (r=0.690, p<0.001). In skin metastases, ALCAM expression was significantly stronger (membranous IRS, 8.76; cytoplasmic IRS, 7.12; p<0.001). Mean staining intensity for CEACAM6 was IRS 3.88. No or weak CEACAM6 and ALCAM staining (IRS 0-3) was seen in 53% vs 27% of all metastases.Compared with CEACAM6, ALCAM showed significantly stronger protein expression in breast cancer skin metastases compared with metastases in all other sites.CONCLUSIONSCompared with CEACAM6, ALCAM showed significantly stronger protein expression in breast cancer skin metastases compared with metastases in all other sites. For prediction and understanding of underlying mechanisms of organ-specific metastases, various gene and protein expression signatures have been identified in primary breast carcinomas. These expression signatures often include several genes coding for adhesion molecules, such as activated leucocyte cell adhesion molecule (ALCAM/CD166) and carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6), both of which may play an important role in the development of distant metastases because of their adherent properties. Owing to their predominantly membranous localisation, they are also considered to have certain therapeutic potential. Apart from expression data obtained in the primary tumour, data for gene and protein expression patterns in distant breast cancer metastases are rare. Therefore this study focuses on analysing the distribution of ALCAM and CEACAM6 protein expression in breast cancer metastases from different sites. Immunohistochemical staining for ALCAM and CEACAM6 in 117 breast cancer metastases derived from liver (n=24), lung (n=19), brain (n=21), bone (n=36) and skin (n=17) was performed. Immunoreactive scores (IRS) for ALCAM in all metastases except skin metastases ranged from 2.63 to 5.10 (membranous) and 2.79 to 3.67 (cytoplasmic), showing a positive correlation with each other (r=0.690, p<0.001). In skin metastases, ALCAM expression was significantly stronger (membranous IRS, 8.76; cytoplasmic IRS, 7.12; p<0.001). Mean staining intensity for CEACAM6 was IRS 3.88. No or weak CEACAM6 and ALCAM staining (IRS 0-3) was seen in 53% vs 27% of all metastases. Compared with CEACAM6, ALCAM showed significantly stronger protein expression in breast cancer skin metastases compared with metastases in all other sites. AimsFor prediction and understanding of underlying mechanisms of organ-specific metastases, various gene and protein expression signatures have been identified in primary breast carcinomas. These expression signatures often include several genes coding for adhesion molecules, such as activated leucocyte cell adhesion molecule (ALCAM/CD166) and carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6), both of which may play an important role in the development of distant metastases because of their adherent properties. Owing to their predominantly membranous localisation, they are also considered to have certain therapeutic potential. Apart from expression data obtained in the primary tumour, data for gene and protein expression patterns in distant breast cancer metastases are rare. Therefore this study focuses on analysing the distribution of ALCAM and CEACAM6 protein expression in breast cancer metastases from different sites.MethodsImmunohistochemical staining for ALCAM and CEACAM6 in 117 breast cancer metastases derived from liver (n=24), lung (n=19), brain (n=21), bone (n=36) and skin (n=17) was performed.ResultsImmunoreactive scores (IRS) for ALCAM in all metastases except skin metastases ranged from 2.63 to 5.10 (membranous) and 2.79 to 3.67 (cytoplasmic), showing a positive correlation with each other (r=0.690, p<0.001). In skin metastases, ALCAM expression was significantly stronger (membranous IRS, 8.76; cytoplasmic IRS, 7.12; p<0.001). Mean staining intensity for CEACAM6 was IRS 3.88. No or weak CEACAM6 and ALCAM staining (IRS 0–3) was seen in 53% vs 27% of all metastases.ConclusionsCompared with CEACAM6, ALCAM showed significantly stronger protein expression in breast cancer skin metastases compared with metastases in all other sites. Aims For prediction and understanding of underlying mechanisms of organ-specific metastases, various gene and protein expression signatures have been identified in primary breast carcinomas. These expression signatures often include several genes coding for adhesion molecules, such as activated leucocyte cell adhesion molecule (ALCAM/CD166) and carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6), both of which may play an important role in the development of distant metastases because of their adherent properties. Owing to their predominantly membranous localisation, they are also considered to have certain therapeutic potential. Apart from expression data obtained in the primary tumour, data for gene and protein expression patterns in distant breast cancer metastases are rare. Therefore this study focuses on analysing the distribution of ALCAM and CEACAM6 protein expression in breast cancer metastases from different sites. Methods Immunohistochemical staining for ALCAM and CEACAM6 in 117 breast cancer metastases derived from liver (n=24), lung (n=19), brain (n=21), bone (n=36) and skin (n=17) was performed. Results Immunoreactive scores (IRS) for ALCAM in all metastases except skin metastases ranged from 2.63 to 5.10 (membranous) and 2.79 to 3.67 (cytoplasmic), showing a positive correlation with each other (r=0.690, p<0.001). In skin metastases, ALCAM expression was significantly stronger (membranous IRS, 8.76; cytoplasmic IRS, 7.12; p<0.001). Mean staining intensity for CEACAM6 was IRS 3.88. No or weak CEACAM6 and ALCAM staining (IRS 0-3) was seen in 53% vs 27% of all metastases. Conclusions Compared with CEACAM6, ALCAM showed significantly stronger protein expression in breast cancer skin metastases compared with metastases in all other sites. |
Author | Müller, Volkmar Jänicke, Fritz Höller, Sylvia Hagel, Christian Köhler, Nadine Kilic, Ergin Milde-Langosch, Karin Ihnen, Maike Kersten, Jan F Löning, Thomas Witzel, Isabell |
Author_xml | – sequence: 1 givenname: Maike surname: Ihnen fullname: Ihnen, Maike email: maihnen@gmx.ch organization: Department of Gynaecology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany – sequence: 2 givenname: Ergin surname: Kilic fullname: Kilic, Ergin email: maihnen@gmx.ch organization: Institute for Pathology, University Hospital Basel, Basel, Switzerland – sequence: 3 givenname: Nadine surname: Köhler fullname: Köhler, Nadine email: maihnen@gmx.ch organization: Department of Gynaecology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany – sequence: 4 givenname: Thomas surname: Löning fullname: Löning, Thomas email: maihnen@gmx.ch organization: Albertinen Pathologie Hamburg, Albertinen Hospital, Hamburg, Germany – sequence: 5 givenname: Isabell surname: Witzel fullname: Witzel, Isabell email: maihnen@gmx.ch organization: Department of Gynaecology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany – sequence: 6 givenname: Christian surname: Hagel fullname: Hagel, Christian email: maihnen@gmx.ch organization: Department of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany – sequence: 7 givenname: Sylvia surname: Höller fullname: Höller, Sylvia email: maihnen@gmx.ch organization: Institute for Pathology, University Hospital Basel, Basel, Switzerland – sequence: 8 givenname: Jan F surname: Kersten fullname: Kersten, Jan F email: maihnen@gmx.ch organization: Department of Medical Biometry and Epidemiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany – sequence: 9 givenname: Volkmar surname: Müller fullname: Müller, Volkmar email: maihnen@gmx.ch organization: Department of Gynaecology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany – sequence: 10 givenname: Fritz surname: Jänicke fullname: Jänicke, Fritz email: maihnen@gmx.ch organization: Department of Gynaecology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany – sequence: 11 givenname: Karin surname: Milde-Langosch fullname: Milde-Langosch, Karin email: maihnen@gmx.ch organization: Department of Gynaecology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany |
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Keywords | Mammary gland diseases Anatomic pathology Breast disease Cell adhesion molecule Activated leukocyte cell adhesion molecule Breast cancer Skin Malignant tumor Metastasis Cancer |
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Snippet | AimsFor prediction and understanding of underlying mechanisms of organ-specific metastases, various gene and protein expression signatures have been identified... Aims For prediction and understanding of underlying mechanisms of organ-specific metastases, various gene and protein expression signatures have been... For prediction and understanding of underlying mechanisms of organ-specific metastases, various gene and protein expression signatures have been identified in... |
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SubjectTerms | adhesion molecule Adult Aged Aged, 80 and over ALCAM Antigens, CD - metabolism Biological and medical sciences Bone Neoplasms - metabolism Bone Neoplasms - secondary Brain Neoplasms - metabolism Brain Neoplasms - secondary breast cancer metastasis Breast Neoplasms - metabolism CEACAM6 Cell Adhesion Molecules - metabolism Cell Adhesion Molecules, Neuronal - metabolism Female Fetal Proteins - metabolism GPI-Linked Proteins - metabolism Gynecology. Andrology. Obstetrics Humans Investigative techniques, diagnostic techniques (general aspects) Liver Neoplasms - metabolism Liver Neoplasms - secondary Lung Neoplasms - metabolism Lung Neoplasms - secondary Mammary gland diseases Medical sciences Middle Aged Neoplasm Proteins - metabolism Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques skin metastasis Skin Neoplasms - metabolism Skin Neoplasms - secondary Tumors |
Title | Protein expression analysis of ALCAM and CEACAM6 in breast cancer metastases reveals significantly increased ALCAM expression in metastases of the skin |
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