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NY‐ESO‐1 protein expression in primary breast carcinoma and metastases—correlation with CD8+ T‐cell and CD79a+ plasmacytic/B‐cell infiltration
International journal of cancer, 2007-06, Vol.120 (11), p.2411-2417
Theurillat, Jean‐Philippe
Ingold, Fabienne
Frei, Claudia
Zippelius, Alfred
Varga, Zsuzsanna
Seifert, Burkhardt
Chen, Yao‐Tseng
Jäger, Dirk
Knuth, Alexander
Moch, Holger
2007
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Theurillat, Jean‐Philippe
Ingold, Fabienne
Frei, Claudia
Zippelius, Alfred
Varga, Zsuzsanna
Seifert, Burkhardt
Chen, Yao‐Tseng
Jäger, Dirk
Knuth, Alexander
Moch, Holger
Titel
NY‐ESO‐1 protein expression in primary breast carcinoma and metastases—correlation with CD8+ T‐cell and CD79a+ plasmacytic/B‐cell infiltration
Ist Teil von
International journal of cancer, 2007-06, Vol.120 (11), p.2411-2417
Ort / Verlag
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Erscheinungsjahr
2007
Quelle
Wiley-Blackwell Journals
Beschreibungen/Notizen
NY‐ESO‐1 is a cancer testis antigen expressed in various malignancies and testicular germ cells. Because of its capacity to induce specific humoral and cellular immunity in patients with NY‐ESO‐1‐positive carcinomas, it represents a promising target for cancer immunotherapy. In breast cancer, NY‐ESO‐1‐mRNA was reported in up to 42%, but protein expression has not been determined to larger extent. In the present tissue microarray‐based study, primary breast cancers (n = 1,444), in situ lesion (n = 148), recurrences (n = 88), lymph node (n = 525) and distant metastases (n = 91) were studied for NY‐ESO‐1 expression by immunohistochemistry. NY‐ESO‐1‐protein expression was compared with mRNA expression by real‐time PCR. NY‐ESO‐1‐protein was detected in 3.1% (4/128) in situ lesions and in 2.1% (28/1355) invasive breast cancer. There were 1.8% (9/493) NY‐ESO‐1‐positive lymph node and 5.1% (4/78) positive distant metastases. NY‐ESO‐1 was more frequently expressed in grade 3 (4.9%) than in grade 2 (0.8%) and grade 1 (0.5%) carcinomas (p < 0.0001). Presence of tumor‐infiltrating CD8+ T‐cells correlated with NY‐ESO‐1 (p < 0.0001) on the tissue microarray. On randomly selected large sections, 4 out of 9 NY‐ESO‐1‐positive tumors displayed a brisk infiltrate of CD79a+ plasmocytes/B‐cells, but none of 10 NY‐ESO‐1‐negative tumors (p < 0.05). NY‐ESO‐1‐mRNA expression was detected in frozen samples of NY‐ESO‐1‐protein positive (n = 6) and negative breast cancers (n = 8) and in normal testis. Comparison between mRNA and protein expression revealed that only breast cancers with NY‐ESO‐1‐mRNA levels comparable or higher than testis expressed NY‐ESO‐1‐protein. These findings suggest that NY‐ESO‐1‐positive breast cancers represent a small subset of poorly differentiated tumors with evidence of cellular and humoral immune response. © 2007 Wiley‐Liss, Inc.
Sprache
Englisch
Identifikatoren
ISSN: 0020-7136
eISSN: 1097-0215
DOI: 10.1002/ijc.22376
Titel-ID: cdi_proquest_miscellaneous_70347121
Format
–
Schlagworte
Adolescent
,
Adult
,
Aged
,
Aged, 80 and over
,
Antigens, Neoplasm - metabolism
,
B-Lymphocytes - immunology
,
Biological and medical sciences
,
breast cancer
,
Breast Neoplasms - immunology
,
Breast Neoplasms - metabolism
,
cancer testis antigen
,
CD79 Antigens - immunology
,
CD8-Positive T-Lymphocytes - immunology
,
Female
,
Gynecology. Andrology. Obstetrics
,
Humans
,
Immunohistochemistry
,
In Situ Hybridization, Fluorescence
,
Lymphocytes, Tumor-Infiltrating - immunology
,
Mammary gland diseases
,
Medical sciences
,
Membrane Proteins - metabolism
,
Middle Aged
,
NY‐ESO‐1
,
Polymerase Chain Reaction
,
tissue microarray
,
Tumors
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