Localization of thymosin ß-4 in tumors

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Localization of thymosin ß-4 in tumors. / Larsson, Lars-Inge; Holck, Susanne.

I: Annals of the New York Academy of Sciences, Bind 1112, 2007, s. 317-325.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Larsson, L-I & Holck, S 2007, 'Localization of thymosin ß-4 in tumors', Annals of the New York Academy of Sciences, bind 1112, s. 317-325. https://doi.org/10.1196/annals.1415.005

APA

Larsson, L-I., & Holck, S. (2007). Localization of thymosin ß-4 in tumors. Annals of the New York Academy of Sciences, 1112, 317-325. https://doi.org/10.1196/annals.1415.005

Vancouver

Larsson L-I, Holck S. Localization of thymosin ß-4 in tumors. Annals of the New York Academy of Sciences. 2007;1112:317-325. https://doi.org/10.1196/annals.1415.005

Author

Larsson, Lars-Inge ; Holck, Susanne. / Localization of thymosin ß-4 in tumors. I: Annals of the New York Academy of Sciences. 2007 ; Bind 1112. s. 317-325.

Bibtex

@article{dd5d0090a1c211ddb6ae000ea68e967b,
title = "Localization of thymosin {\ss}-4 in tumors",
abstract = "Overexpression of thymosin {\ss}-4 has been linked to malignant progression but the localization of this polypeptide within tumor is incompletely known. We therefore examined breast cancers for thymosin {\ss}-4 using immunofluorescence. Reactive cells were identified with monoclonal cell marker antibodies. A very heterogeneous staining pattern for thymosin {\ss}-4 was observed. Thus, while leukocytes and macrophages showed intense reactivity for this polypeptide, cancer cells, and endothelial cells showed a much more variable reactivity. A similar heterogeneous staining was observed also in colorectal carcinomas. The degree of staining of breast cancer cells for thymosin {\ss}-4 correlated neither to histological grade nor to endothelial cell staining. However, therewas a tendency toward correlation (P = 0.07) between staining of endothelial cells and histological grade. Treatment of cultured breast cancer cells (SK-BR-3) with 1-4 µg thymosin {\ss}-4/mL significantly increased cell numbers, as determined by MTT-assays. These data reveal an unexpected cellular heterogeneity of thymosin {\ss}-4 expression in breast and colonic carcinomas and suggest that local release of this polypeptide in the tumor microenvironment may modulate tumor behavior.",
keywords = "Former LIFE faculty, thomosin {\ss}-4, cancer, colorectal, breast, endothelial cells, macrophages",
author = "Lars-Inge Larsson and Susanne Holck",
note = "Thymosins in Health and Disease First International Symposium",
year = "2007",
doi = "10.1196/annals.1415.005",
language = "English",
volume = "1112",
pages = "317--325",
journal = "Annals of The Lyceum of Natural History of New York",
issn = "0077-8923",
publisher = "Wiley-Blackwell",

}

RIS

TY - JOUR

T1 - Localization of thymosin ß-4 in tumors

AU - Larsson, Lars-Inge

AU - Holck, Susanne

N1 - Thymosins in Health and Disease First International Symposium

PY - 2007

Y1 - 2007

N2 - Overexpression of thymosin ß-4 has been linked to malignant progression but the localization of this polypeptide within tumor is incompletely known. We therefore examined breast cancers for thymosin ß-4 using immunofluorescence. Reactive cells were identified with monoclonal cell marker antibodies. A very heterogeneous staining pattern for thymosin ß-4 was observed. Thus, while leukocytes and macrophages showed intense reactivity for this polypeptide, cancer cells, and endothelial cells showed a much more variable reactivity. A similar heterogeneous staining was observed also in colorectal carcinomas. The degree of staining of breast cancer cells for thymosin ß-4 correlated neither to histological grade nor to endothelial cell staining. However, therewas a tendency toward correlation (P = 0.07) between staining of endothelial cells and histological grade. Treatment of cultured breast cancer cells (SK-BR-3) with 1-4 µg thymosin ß-4/mL significantly increased cell numbers, as determined by MTT-assays. These data reveal an unexpected cellular heterogeneity of thymosin ß-4 expression in breast and colonic carcinomas and suggest that local release of this polypeptide in the tumor microenvironment may modulate tumor behavior.

AB - Overexpression of thymosin ß-4 has been linked to malignant progression but the localization of this polypeptide within tumor is incompletely known. We therefore examined breast cancers for thymosin ß-4 using immunofluorescence. Reactive cells were identified with monoclonal cell marker antibodies. A very heterogeneous staining pattern for thymosin ß-4 was observed. Thus, while leukocytes and macrophages showed intense reactivity for this polypeptide, cancer cells, and endothelial cells showed a much more variable reactivity. A similar heterogeneous staining was observed also in colorectal carcinomas. The degree of staining of breast cancer cells for thymosin ß-4 correlated neither to histological grade nor to endothelial cell staining. However, therewas a tendency toward correlation (P = 0.07) between staining of endothelial cells and histological grade. Treatment of cultured breast cancer cells (SK-BR-3) with 1-4 µg thymosin ß-4/mL significantly increased cell numbers, as determined by MTT-assays. These data reveal an unexpected cellular heterogeneity of thymosin ß-4 expression in breast and colonic carcinomas and suggest that local release of this polypeptide in the tumor microenvironment may modulate tumor behavior.

KW - Former LIFE faculty

KW - thomosin ß-4

KW - cancer

KW - colorectal

KW - breast

KW - endothelial cells

KW - macrophages

U2 - 10.1196/annals.1415.005

DO - 10.1196/annals.1415.005

M3 - Journal article

C2 - 17495241

VL - 1112

SP - 317

EP - 325

JO - Annals of The Lyceum of Natural History of New York

JF - Annals of The Lyceum of Natural History of New York

SN - 0077-8923

ER -

ID: 8081204