CEACAM1 expression in cutaneous malignant melanoma predicts the development of metastatic disease.

Standard

CEACAM1 expression in cutaneous malignant melanoma predicts the development of metastatic disease. / Dahl, Anka; Moll, Ingrid; Berger, Jürgen; Wagener, Christoph; Brümmer, Jens; Schulze, Hans-Joachim; Brunner, Georg; Schumacher, Udo.

in: J CLIN ONCOL, Jahrgang 20, Nr. 10, 10, 2002, S. 2530-2536.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Dahl, A, Moll, I, Berger, J, Wagener, C, Brümmer, J, Schulze, H-J, Brunner, G & Schumacher, U 2002, 'CEACAM1 expression in cutaneous malignant melanoma predicts the development of metastatic disease.', J CLIN ONCOL, Jg. 20, Nr. 10, 10, S. 2530-2536. <http://www.ncbi.nlm.nih.gov/pubmed/12011132?dopt=Citation>

APA

Dahl, A., Moll, I., Berger, J., Wagener, C., Brümmer, J., Schulze, H-J., Brunner, G., & Schumacher, U. (2002). CEACAM1 expression in cutaneous malignant melanoma predicts the development of metastatic disease. J CLIN ONCOL, 20(10), 2530-2536. [10]. http://www.ncbi.nlm.nih.gov/pubmed/12011132?dopt=Citation

Vancouver

Dahl A, Moll I, Berger J, Wagener C, Brümmer J, Schulze H-J et al. CEACAM1 expression in cutaneous malignant melanoma predicts the development of metastatic disease. J CLIN ONCOL. 2002;20(10):2530-2536. 10.

Bibtex

@article{2f42bcff25c540ff841b898909a3d710,
title = "CEACAM1 expression in cutaneous malignant melanoma predicts the development of metastatic disease.",
abstract = "PURPOSE: The cell adhesion molecule CEACAM1 is involved in intercellular adhesion and subsequent signal transduction events in a number of epithelia. CEACAM1 downregulation has been demonstrated in colorectal and prostate carcinomas. This study sought to analyze whether its expression in malignant melanoma is associated with metastasis. PATIENTS AND METHODS: CEACAM1 expression was immunohistochemically evaluated in 100 primary cutaneous malignant melanomas and correlated with metastasis in a 10-year follow-up. Furthermore, CEACAM1 expression was analyzed in metastatic lesions (11 distant metastases and six sentinel lymph node metastases). Univariate Kaplan-Meier analysis and multivariate Cox proportional hazard regression analysis adjusted for standard prognostic indicators were performed to assess the prognostic relevance of CEACAM1 expression. RESULTS: A total of 28 of 40 patients with CEACAM1-positive primary melanomas developed metastatic disease, compared with only six of 60 patients with CEACAM1-negative melanomas. Often, the strongest CEACAM1 expression was observed at the invading front. In addition, CEACAM1 expression was preserved in the metastatic lesions. Kaplan-Meier analysis revealed a highly significant association between CEACAM1 expression and metastasis (P",
author = "Anka Dahl and Ingrid Moll and J{\"u}rgen Berger and Christoph Wagener and Jens Br{\"u}mmer and Hans-Joachim Schulze and Georg Brunner and Udo Schumacher",
year = "2002",
language = "Deutsch",
volume = "20",
pages = "2530--2536",
journal = "J CLIN ONCOL",
issn = "0732-183X",
publisher = "American Society of Clinical Oncology",
number = "10",

}

RIS

TY - JOUR

T1 - CEACAM1 expression in cutaneous malignant melanoma predicts the development of metastatic disease.

AU - Dahl, Anka

AU - Moll, Ingrid

AU - Berger, Jürgen

AU - Wagener, Christoph

AU - Brümmer, Jens

AU - Schulze, Hans-Joachim

AU - Brunner, Georg

AU - Schumacher, Udo

PY - 2002

Y1 - 2002

N2 - PURPOSE: The cell adhesion molecule CEACAM1 is involved in intercellular adhesion and subsequent signal transduction events in a number of epithelia. CEACAM1 downregulation has been demonstrated in colorectal and prostate carcinomas. This study sought to analyze whether its expression in malignant melanoma is associated with metastasis. PATIENTS AND METHODS: CEACAM1 expression was immunohistochemically evaluated in 100 primary cutaneous malignant melanomas and correlated with metastasis in a 10-year follow-up. Furthermore, CEACAM1 expression was analyzed in metastatic lesions (11 distant metastases and six sentinel lymph node metastases). Univariate Kaplan-Meier analysis and multivariate Cox proportional hazard regression analysis adjusted for standard prognostic indicators were performed to assess the prognostic relevance of CEACAM1 expression. RESULTS: A total of 28 of 40 patients with CEACAM1-positive primary melanomas developed metastatic disease, compared with only six of 60 patients with CEACAM1-negative melanomas. Often, the strongest CEACAM1 expression was observed at the invading front. In addition, CEACAM1 expression was preserved in the metastatic lesions. Kaplan-Meier analysis revealed a highly significant association between CEACAM1 expression and metastasis (P

AB - PURPOSE: The cell adhesion molecule CEACAM1 is involved in intercellular adhesion and subsequent signal transduction events in a number of epithelia. CEACAM1 downregulation has been demonstrated in colorectal and prostate carcinomas. This study sought to analyze whether its expression in malignant melanoma is associated with metastasis. PATIENTS AND METHODS: CEACAM1 expression was immunohistochemically evaluated in 100 primary cutaneous malignant melanomas and correlated with metastasis in a 10-year follow-up. Furthermore, CEACAM1 expression was analyzed in metastatic lesions (11 distant metastases and six sentinel lymph node metastases). Univariate Kaplan-Meier analysis and multivariate Cox proportional hazard regression analysis adjusted for standard prognostic indicators were performed to assess the prognostic relevance of CEACAM1 expression. RESULTS: A total of 28 of 40 patients with CEACAM1-positive primary melanomas developed metastatic disease, compared with only six of 60 patients with CEACAM1-negative melanomas. Often, the strongest CEACAM1 expression was observed at the invading front. In addition, CEACAM1 expression was preserved in the metastatic lesions. Kaplan-Meier analysis revealed a highly significant association between CEACAM1 expression and metastasis (P

M3 - SCORING: Zeitschriftenaufsatz

VL - 20

SP - 2530

EP - 2536

JO - J CLIN ONCOL

JF - J CLIN ONCOL

SN - 0732-183X

IS - 10

M1 - 10

ER -