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SHR Neuro Cancer Cardio Lipid Metab Microb

Deutsch, AJA; Rinner, B; Pichler, M; Prochazka, K; Pansy, K; Bischof, M; Fechter, K; Hatzl, S; Feichtinger, J; Wenzl, K; Frisch, MT; Stiegelbauer, V; Prokesch, A; Krogsdam, A; Sill, H; Thallinger, GG; Greinix, HT; Wang, C; Beham-Schmid, C; Neumeister, P.
NR4A3 Suppresses Lymphomagenesis through Induction of Proapoptotic Genes.
Cancer Res. 2017; 77(9):2375-2386 Doi: 10.1158/0008-5472.CAN-16-2320 [OPEN ACCESS]
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Leading authors Med Uni Graz
Deutsch Alexander
Co-authors Med Uni Graz
Beham-Schmid Christine
Fechter Karoline
Feichtinger Julia
Greinix Hildegard
Hatzl Stefan
Melcher Marie-Therese
Neumeister Peter
Pansy Katrin
Pichler Martin
Prochazka Katharina
Prokesch Andreas
Rinner Beate
Sill Heinz
Stiegelbauer Verena
Wenzl Kerstin
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Abstract:
Nuclear orphan receptor NR4A1 exerts an essential tumor suppressor function in aggressive lymphomas. In this study, we investigated the hypothesized contribution of the related NR4A family member NR4A3 to lymphomagenesis. In aggressive lymphoma patients, low expression of NR4A3 was associated with poor survival. Ectopic expression or pharmacological activation of NR4A3 in lymphoma cell lines led to a significantly higher proportion of apoptotic cells. In a mouse NSG xenograft model of lymphoma (stably transduced SuDHL4 cells), NR4A3 expression abrogated tumor growth, compared with vector control and uninduced cells that formed massive tumors. Transcript analysis of four different aggressive lymphoma cell lines overexpressing either NR4A3 or NR4A1 revealed that apoptosis was driven similarly by induction of BAK, Puma, BIK, BIM, BID, and Trail. Overall, our results showed that NR4A3 possesses robust tumor suppressor functions of similar impact to NR4A1 in aggressive lymphomas. Cancer Res; 77(9); 2375-86. ©2017 AACR. ©2017 American Association for Cancer Research.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Apoptosis - genetics
Carcinogenesis - genetics
Cell Line, Tumor -
Cell Proliferation - genetics
DNA-Binding Proteins - biosynthesis
DNA-Binding Proteins - genetics
Disease-Free Survival -
Female -
Gene Expression Regulation, Neoplastic -
Humans -
Kaplan-Meier Estimate -
Lymphoma - genetics
Lymphoma - pathology
Male -
Mice -
Receptors, Steroid - biosynthesis
Receptors, Steroid - genetics
Receptors, Thyroid Hormone - biosynthesis
Receptors, Thyroid Hormone - genetics
Xenograft Model Antitumor Assays -

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