DARPP-32 and t-DARPP promote non-small cell lung cancer growth through regulation of IKKα-dependent cell migration

Sk Kayum Alam, Matteo Astone, Ping Liu, Stephanie R. Hall, Abbygail M. Coyle, Erin N. Dankert, Dane K. Hoffman, Wei Zhang, Rui Kuang, Anja Roden, Aaron Mansfield, Luke H. Hoeppner

Research output: Contribution to journalArticle

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Abstract

Lung cancer is the leading cause of cancer-related death worldwide. Here we demonstrate that elevated expression of dopamine and cyclic adenosine monophosphate-regulated phosphoprotein, Mr 32000 (DARPP-32), and its truncated splice variant t-DARPP promote lung tumor growth, while abrogation of DARPP-32 expression in human non-small-cell lung cancer (NSCLC) cells reduces tumor growth in orthotopic mouse models. We observe a physical interaction between DARPP-32 and inhibitory kappa B kinase-α (IKKα) that promotes NSCLC cell migration through non-canonical nuclear factor kappa-light-chain-enhancer of activated B cells 2 (NF-κB2) signaling. Bioinformatics analysis of 513 lung adenocarcinoma patients reveals that elevated t-DARPP isoform expression is associated with poor overall survival. Histopathological investigation of 62 human lung adenocarcinoma tissues also shows that t-DARPP expression is elevated with increasing tumor (T) stage. Our data suggest that DARPP-32 isoforms serve as a negative prognostic marker associated with increasing stages of NSCLC and may represent a novel therapeutic target.

Original languageEnglish (US)
Article number43
JournalCommunications Biology
Volume1
Issue number1
DOIs
StatePublished - Dec 1 2018

Fingerprint

phosphoproteins
Phosphoproteins
cyclic AMP
lung neoplasms
dopamine
cell movement
Non-Small Cell Lung Carcinoma
Cyclic AMP
Cell Movement
Dopamine
phosphotransferases (kinases)
Phosphotransferases
Cells
Tumors
Growth
Neoplasms
Protein Isoforms
adenocarcinoma
neoplasms
cells

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Agricultural and Biological Sciences(all)
  • Medicine (miscellaneous)

Cite this

Alam, S. K., Astone, M., Liu, P., Hall, S. R., Coyle, A. M., Dankert, E. N., ... Hoeppner, L. H. (2018). DARPP-32 and t-DARPP promote non-small cell lung cancer growth through regulation of IKKα-dependent cell migration. Communications Biology, 1(1), [43]. https://doi.org/10.1038/s42003-018-0050-6

DARPP-32 and t-DARPP promote non-small cell lung cancer growth through regulation of IKKα-dependent cell migration. / Alam, Sk Kayum; Astone, Matteo; Liu, Ping; Hall, Stephanie R.; Coyle, Abbygail M.; Dankert, Erin N.; Hoffman, Dane K.; Zhang, Wei; Kuang, Rui; Roden, Anja; Mansfield, Aaron; Hoeppner, Luke H.

In: Communications Biology, Vol. 1, No. 1, 43, 01.12.2018.

Research output: Contribution to journalArticle

Alam, SK, Astone, M, Liu, P, Hall, SR, Coyle, AM, Dankert, EN, Hoffman, DK, Zhang, W, Kuang, R, Roden, A, Mansfield, A & Hoeppner, LH 2018, 'DARPP-32 and t-DARPP promote non-small cell lung cancer growth through regulation of IKKα-dependent cell migration', Communications Biology, vol. 1, no. 1, 43. https://doi.org/10.1038/s42003-018-0050-6
Alam, Sk Kayum ; Astone, Matteo ; Liu, Ping ; Hall, Stephanie R. ; Coyle, Abbygail M. ; Dankert, Erin N. ; Hoffman, Dane K. ; Zhang, Wei ; Kuang, Rui ; Roden, Anja ; Mansfield, Aaron ; Hoeppner, Luke H. / DARPP-32 and t-DARPP promote non-small cell lung cancer growth through regulation of IKKα-dependent cell migration. In: Communications Biology. 2018 ; Vol. 1, No. 1.
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