Downstream targets of Nm23-H1: gene expression profiling of CAL 27 cells using DNA microarray.

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Downstream targets of Nm23-H1: gene expression profiling of CAL 27 cells using DNA microarray. / Bosnar, Maja Herak; Bago, Ruzica; Gall-Troselj, Koraljka; Streichert, Thomas; Paveli, Jasminka.

in: MOL CARCINOGEN, Jahrgang 45, Nr. 8, 8, 2006, S. 627-633.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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Bosnar MH, Bago R, Gall-Troselj K, Streichert T, Paveli J. Downstream targets of Nm23-H1: gene expression profiling of CAL 27 cells using DNA microarray. MOL CARCINOGEN. 2006;45(8):627-633. 8.

Bibtex

@article{7bf5292ffb9c4853b210a3e972bb8fd8,
title = "Downstream targets of Nm23-H1: gene expression profiling of CAL 27 cells using DNA microarray.",
abstract = "The human nm23-H1 was discovered as a tumor metastasis suppressor based on its reduced expression in melanoma cell lines with low versus high metastatic potential. It encodes for one of two subunits of the nucleoside-diphosphate kinase. Besides its role in the maintenance of the cells NTP pool, nm23 plays a key role in different cellular processes. The role of nm23-H1 in these processes still has to be elucidated. Our goal was to identify Nm23-H1 downstream targets by subjecting Nm23-H1 overexpressing CAL 27 cells oral squamous cell carcinoma (OSSC) to microarray analysis. The genes with changed expression patterns could be clustered into several groups: transforming growth factor beta (TGFbeta) signaling pathway, cell adhesion, invasion and motility, proteasome machinery, cell-cycle, epithelial structural and related molecules and others. Based on the expression patterns observed we presume that nm23-H1 might have a role in OSSCs, which should be confirmed by future experiments.",
author = "Bosnar, {Maja Herak} and Ruzica Bago and Koraljka Gall-Troselj and Thomas Streichert and Jasminka Paveli",
year = "2006",
language = "Deutsch",
volume = "45",
pages = "627--633",
journal = "MOL CARCINOGEN",
issn = "0899-1987",
publisher = "Wiley-Liss Inc.",
number = "8",

}

RIS

TY - JOUR

T1 - Downstream targets of Nm23-H1: gene expression profiling of CAL 27 cells using DNA microarray.

AU - Bosnar, Maja Herak

AU - Bago, Ruzica

AU - Gall-Troselj, Koraljka

AU - Streichert, Thomas

AU - Paveli, Jasminka

PY - 2006

Y1 - 2006

N2 - The human nm23-H1 was discovered as a tumor metastasis suppressor based on its reduced expression in melanoma cell lines with low versus high metastatic potential. It encodes for one of two subunits of the nucleoside-diphosphate kinase. Besides its role in the maintenance of the cells NTP pool, nm23 plays a key role in different cellular processes. The role of nm23-H1 in these processes still has to be elucidated. Our goal was to identify Nm23-H1 downstream targets by subjecting Nm23-H1 overexpressing CAL 27 cells oral squamous cell carcinoma (OSSC) to microarray analysis. The genes with changed expression patterns could be clustered into several groups: transforming growth factor beta (TGFbeta) signaling pathway, cell adhesion, invasion and motility, proteasome machinery, cell-cycle, epithelial structural and related molecules and others. Based on the expression patterns observed we presume that nm23-H1 might have a role in OSSCs, which should be confirmed by future experiments.

AB - The human nm23-H1 was discovered as a tumor metastasis suppressor based on its reduced expression in melanoma cell lines with low versus high metastatic potential. It encodes for one of two subunits of the nucleoside-diphosphate kinase. Besides its role in the maintenance of the cells NTP pool, nm23 plays a key role in different cellular processes. The role of nm23-H1 in these processes still has to be elucidated. Our goal was to identify Nm23-H1 downstream targets by subjecting Nm23-H1 overexpressing CAL 27 cells oral squamous cell carcinoma (OSSC) to microarray analysis. The genes with changed expression patterns could be clustered into several groups: transforming growth factor beta (TGFbeta) signaling pathway, cell adhesion, invasion and motility, proteasome machinery, cell-cycle, epithelial structural and related molecules and others. Based on the expression patterns observed we presume that nm23-H1 might have a role in OSSCs, which should be confirmed by future experiments.

M3 - SCORING: Zeitschriftenaufsatz

VL - 45

SP - 627

EP - 633

JO - MOL CARCINOGEN

JF - MOL CARCINOGEN

SN - 0899-1987

IS - 8

M1 - 8

ER -