Expression of human milk fat globulin proteins in cells of haemopoietic origin.

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Expression of human milk fat globulin proteins in cells of haemopoietic origin. / Krüger, W; Lohner, R; Jung, Roman; Kröger, N; Zander, A R.

In: BRIT J CANCER, Vol. 83, No. 7, 7, 2000, p. 874-879.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Krüger, W, Lohner, R, Jung, R, Kröger, N & Zander, AR 2000, 'Expression of human milk fat globulin proteins in cells of haemopoietic origin.', BRIT J CANCER, vol. 83, no. 7, 7, pp. 874-879. <http://www.ncbi.nlm.nih.gov/pubmed/10970688?dopt=Citation>

APA

Vancouver

Krüger W, Lohner R, Jung R, Kröger N, Zander AR. Expression of human milk fat globulin proteins in cells of haemopoietic origin. BRIT J CANCER. 2000;83(7):874-879. 7.

Bibtex

@article{42d3e5a3b05145e09d2dd07c22bc587a,
title = "Expression of human milk fat globulin proteins in cells of haemopoietic origin.",
abstract = "Lineage-specific gene expression has been used for the identification of metastasis of cancers with unknown primary site or of disseminated cancer cells in haemopoietic compartments such as bone marrow or in lymph nodes. For the muc1, cytokeratin-19 and the CEA genes, the transcription in haemopoietic cells has been shown recently. Here, the expression of the mammary epithelium related antigens BA46 (lactadherin) and BA70 in lymphoid and myeloid cell lines, and in clinical specimens is analysed. By Northern-hybridization with specific oligonucleotides an ubiquitous transcription of both genes, independent from the provenance of cells or the chromosomal gender was found. Both mRNA molecules were amplified by rtPCR from the samples and the specificity could be confirmed by sequence analysis. Peptide-specific antibodies were raised in rabbits and used for Western-blot analysis and for immunocytochemical studies. Both antibodies reacted with total cell lysates from myeloid and lymphatic cells. In immunocytochemistry antibody P717 (anti-lactadherin) had a significant strong staining of the myeloid cell lines K562 and HL60 suggesting a participation of lactadherin in leukocyte-function. Using antibody P718, strong stains were seen in myeloid line K562 and lymphoid line ST486. In conclusion, our findings expand the results that the concept of lineage-specific gene expression is no longer valid at the molecular level.",
author = "W Kr{\"u}ger and R Lohner and Roman Jung and N Kr{\"o}ger and Zander, {A R}",
year = "2000",
language = "Deutsch",
volume = "83",
pages = "874--879",
journal = "BRIT J CANCER",
issn = "0007-0920",
publisher = "NATURE PUBLISHING GROUP",
number = "7",

}

RIS

TY - JOUR

T1 - Expression of human milk fat globulin proteins in cells of haemopoietic origin.

AU - Krüger, W

AU - Lohner, R

AU - Jung, Roman

AU - Kröger, N

AU - Zander, A R

PY - 2000

Y1 - 2000

N2 - Lineage-specific gene expression has been used for the identification of metastasis of cancers with unknown primary site or of disseminated cancer cells in haemopoietic compartments such as bone marrow or in lymph nodes. For the muc1, cytokeratin-19 and the CEA genes, the transcription in haemopoietic cells has been shown recently. Here, the expression of the mammary epithelium related antigens BA46 (lactadherin) and BA70 in lymphoid and myeloid cell lines, and in clinical specimens is analysed. By Northern-hybridization with specific oligonucleotides an ubiquitous transcription of both genes, independent from the provenance of cells or the chromosomal gender was found. Both mRNA molecules were amplified by rtPCR from the samples and the specificity could be confirmed by sequence analysis. Peptide-specific antibodies were raised in rabbits and used for Western-blot analysis and for immunocytochemical studies. Both antibodies reacted with total cell lysates from myeloid and lymphatic cells. In immunocytochemistry antibody P717 (anti-lactadherin) had a significant strong staining of the myeloid cell lines K562 and HL60 suggesting a participation of lactadherin in leukocyte-function. Using antibody P718, strong stains were seen in myeloid line K562 and lymphoid line ST486. In conclusion, our findings expand the results that the concept of lineage-specific gene expression is no longer valid at the molecular level.

AB - Lineage-specific gene expression has been used for the identification of metastasis of cancers with unknown primary site or of disseminated cancer cells in haemopoietic compartments such as bone marrow or in lymph nodes. For the muc1, cytokeratin-19 and the CEA genes, the transcription in haemopoietic cells has been shown recently. Here, the expression of the mammary epithelium related antigens BA46 (lactadherin) and BA70 in lymphoid and myeloid cell lines, and in clinical specimens is analysed. By Northern-hybridization with specific oligonucleotides an ubiquitous transcription of both genes, independent from the provenance of cells or the chromosomal gender was found. Both mRNA molecules were amplified by rtPCR from the samples and the specificity could be confirmed by sequence analysis. Peptide-specific antibodies were raised in rabbits and used for Western-blot analysis and for immunocytochemical studies. Both antibodies reacted with total cell lysates from myeloid and lymphatic cells. In immunocytochemistry antibody P717 (anti-lactadherin) had a significant strong staining of the myeloid cell lines K562 and HL60 suggesting a participation of lactadherin in leukocyte-function. Using antibody P718, strong stains were seen in myeloid line K562 and lymphoid line ST486. In conclusion, our findings expand the results that the concept of lineage-specific gene expression is no longer valid at the molecular level.

M3 - SCORING: Zeitschriftenaufsatz

VL - 83

SP - 874

EP - 879

JO - BRIT J CANCER

JF - BRIT J CANCER

SN - 0007-0920

IS - 7

M1 - 7

ER -