| pubmed-article:1720636 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1720636 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:1720636 | lifeskim:mentions | umls-concept:C0005953 | lld:lifeskim |
| pubmed-article:1720636 | lifeskim:mentions | umls-concept:C0024623 | lld:lifeskim |
| pubmed-article:1720636 | lifeskim:mentions | umls-concept:C0431085 | lld:lifeskim |
| pubmed-article:1720636 | lifeskim:mentions | umls-concept:C1511790 | lld:lifeskim |
| pubmed-article:1720636 | lifeskim:mentions | umls-concept:C0237881 | lld:lifeskim |
| pubmed-article:1720636 | lifeskim:mentions | umls-concept:C0220901 | lld:lifeskim |
| pubmed-article:1720636 | lifeskim:mentions | umls-concept:C0750502 | lld:lifeskim |
| pubmed-article:1720636 | lifeskim:mentions | umls-concept:C1879746 | lld:lifeskim |
| pubmed-article:1720636 | lifeskim:mentions | umls-concept:C1547011 | lld:lifeskim |
| pubmed-article:1720636 | pubmed:issue | 11 | lld:pubmed |
| pubmed-article:1720636 | pubmed:dateCreated | 1992-1-16 | lld:pubmed |
| pubmed-article:1720636 | pubmed:abstractText | Monoclonal antibodies (Mab) are potent probes to identify individual tumour cells or small tumour cell clusters in bone marrow. In the present study, various antibodies directed against either cell surface or intracytoplasmic antigens of epithelial cells were assessed for their ability to detect such cells in bone marrow of patients with breast, colorectal and gastric cancer. According to the presented data, monoclonal antibodies against intracellular cytokeratin (CK) components are superior in terms of specificity and sensitivity to antibodies reacting with epitopes of the cell membrane. Using a monoclonal antibody against the cytokeratin polypeptide 18 in connection with the alkaline phosphatase anti-alkaline phosphatase detection system (APAAP), we could detect tumour cells in bone marrow of 34 out of 97 patients with gastric cancer examined at the time of primary surgery. The incidence of positive findings was correlated to established risk factors, such as histological classification and locoregional lymph node involvement. Clinical follow-up studies on 38 patients demonstrated a significantly increased relapse rate in patients presenting with CK-positive cells in their bone marrow at the time of primary surgery. Thus the described technique may help to identify patients with gastric cancer carrying a high risk of early relapse. | lld:pubmed |
| pubmed-article:1720636 | pubmed:language | eng | lld:pubmed |
| pubmed-article:1720636 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1720636 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:1720636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1720636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1720636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1720636 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1720636 | pubmed:issn | 0959-8049 | lld:pubmed |
| pubmed-article:1720636 | pubmed:author | pubmed-author:WitteJJ | lld:pubmed |
| pubmed-article:1720636 | pubmed:author | pubmed-author:RiethmüllerGG | lld:pubmed |
| pubmed-article:1720636 | pubmed:author | pubmed-author:StrobelFF | lld:pubmed |
| pubmed-article:1720636 | pubmed:author | pubmed-author:SchlimokGG | lld:pubmed |
| pubmed-article:1720636 | pubmed:author | pubmed-author:FunkeII | lld:pubmed |
| pubmed-article:1720636 | pubmed:author | pubmed-author:PantelKK | lld:pubmed |
| pubmed-article:1720636 | pubmed:author | pubmed-author:LindemannFF | lld:pubmed |
| pubmed-article:1720636 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1720636 | pubmed:volume | 27 | lld:pubmed |
| pubmed-article:1720636 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1720636 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1720636 | pubmed:pagination | 1461-5 | lld:pubmed |
| pubmed-article:1720636 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:1720636 | pubmed:meshHeading | pubmed-meshheading:1720636-... | lld:pubmed |
| pubmed-article:1720636 | pubmed:meshHeading | pubmed-meshheading:1720636-... | lld:pubmed |
| pubmed-article:1720636 | pubmed:meshHeading | pubmed-meshheading:1720636-... | lld:pubmed |
| pubmed-article:1720636 | pubmed:meshHeading | pubmed-meshheading:1720636-... | lld:pubmed |
| pubmed-article:1720636 | pubmed:meshHeading | pubmed-meshheading:1720636-... | lld:pubmed |
| pubmed-article:1720636 | pubmed:meshHeading | pubmed-meshheading:1720636-... | lld:pubmed |
| pubmed-article:1720636 | pubmed:meshHeading | pubmed-meshheading:1720636-... | lld:pubmed |
| pubmed-article:1720636 | pubmed:meshHeading | pubmed-meshheading:1720636-... | lld:pubmed |
| pubmed-article:1720636 | pubmed:meshHeading | pubmed-meshheading:1720636-... | lld:pubmed |
| pubmed-article:1720636 | pubmed:year | 1991 | lld:pubmed |
| pubmed-article:1720636 | pubmed:articleTitle | Micrometastatic tumour cells in bone marrow of patients with gastric cancer: methodological aspects of detection and prognostic significance. | lld:pubmed |
| pubmed-article:1720636 | pubmed:affiliation | Medical Clinic II, Zentralklinikum, Augsburg, Germany. | lld:pubmed |
| pubmed-article:1720636 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1720636 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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