» Articles » PMID: 18172309

Hypoxia Regulates Choline Kinase Expression Through Hypoxia-inducible Factor-1 Alpha Signaling in a Human Prostate Cancer Model

Overview
Journal Cancer Res
Specialty Oncology
Date 2008 Jan 4
PMID 18172309
Citations 83
Authors
Affiliations
Soon will be listed here.
Abstract

The intensity of the total choline (tCho) signal in spectroscopic images of tumors is spatially heterogeneous. The likewise heterogeneous physiologic tumor microenvironment may contribute to this heterogeneity. We therefore investigated the relationship between hypoxia, choline metabolites, and choline kinase (Chk) in a human prostate cancer model. Human PC-3 prostate cancer cells were engineered to express enhanced green fluorescent protein (EGFP) under hypoxic conditions. These PC-3-5HRE-EGFP cells were characterized in culture and as tumors transplanted in mice using (1)H magnetic resonance spectroscopy (MRS) and MRS imaging (MRSI) combined with EGFP fluorescence microscopy and imaging. Hypoxic EGFP-fluorescing tumor regions colocalized with regions of high tCho in combined MRSI and optical imaging studies. Cellular phosphocholine (PC) and tCho concentrations as well as Chk expression levels significantly increased following exposure of PC-3 cells to hypoxia. A putative promoter region located 5' of the translation start site of the human chk-alpha gene was cloned and luciferase (Luc)-based reporter vector constructs were generated. Luc reporter assays provided evidence that some of the putative hypoxia response elements (HRE) within this putative chk-alpha promoter region functioned in vitro. Chromatin immunoprecipitation assays using an antibody against hypoxia-inducible factor (HIF)-1 alpha showed that HIF-1 can directly bind this region of the endogenous chk-alpha promoter in hypoxic PC-3-5HRE-EGFP cells. These data suggest that HIF-1 activation of HREs within the putative chk-alpha promoter region can increase Chk-alpha expression within hypoxic environments, consequently increasing cellular PC and tCho levels within these environments.

Citing Articles

Joint Analysis of Multiple Omics to Describe the Biological Characteristics of Resistant Hypertension.

Wang S, Hu Y, Wang Y, Song Y, Liang D, Yin J J Clin Hypertens (Greenwich). 2024; 27(1):e14961.

PMID: 39716980 PMC: 11774085. DOI: 10.1111/jch.14961.


Association of COX-inhibitors with cancer patients' survival under chemotherapy and radiotherapy regimens: a real-world data retrospective cohort analysis.

Flausino L, Ferreira I, Tuan W, Estevez-Diz M, Chammas R Front Oncol. 2024; 14:1433497.

PMID: 39346725 PMC: 11427433. DOI: 10.3389/fonc.2024.1433497.


Mapping the Fate of Hypoxic Cells Using an Irreversible Fluorescent Switch.

Weinstein A, Gilkes D, Godet I Methods Mol Biol. 2024; 2755:49-61.

PMID: 38319568 DOI: 10.1007/978-1-0716-3633-6_3.


Neurogenesis manifestations of solid tumor and tracer imaging studies: a narrative review.

Huang Y, Xiang B, Manyande A, Xiang H, Xiong J Am J Cancer Res. 2023; 13(3):713-726.

PMID: 37034231 PMC: 10077031.


Altered choline level in atherosclerotic lesions: Upregulation of choline transporter-like protein 1 in human coronary unstable plaque.

Nakamura E, Maekawa K, Saito Y, Matsumoto T, Ogawa M, Komohara Y PLoS One. 2023; 18(2):e0281730.

PMID: 36800352 PMC: 9937458. DOI: 10.1371/journal.pone.0281730.


References
1.
KO K, Cook H, Vance D . Reduction of phosphatidylcholine turnover in a Nb 2 lymphoma cell line after prolactin treatment. A novel mechanism for control of phosphatidylcholine levels in cells. J Biol Chem. 1986; 261(17):7846-52. View

2.
Ramirez de Molina A, Gutierrez R, Ramos M, Silva J, Silva J, Bonilla F . Increased choline kinase activity in human breast carcinomas: clinical evidence for a potential novel antitumor strategy. Oncogene. 2002; 21(27):4317-22. DOI: 10.1038/sj.onc.1205556. View

3.
Neeman M, Degani H . Early estrogen-induced metabolic changes and their inhibition by actinomycin D and cycloheximide in human breast cancer cells: 31P and 13C NMR studies. Proc Natl Acad Sci U S A. 1989; 86(14):5585-9. PMC: 297667. DOI: 10.1073/pnas.86.14.5585. View

4.
Negendank W . Studies of human tumors by MRS: a review. NMR Biomed. 1992; 5(5):303-24. DOI: 10.1002/nbm.1940050518. View

5.
Al-Saffar N, Troy H, Ramirez de Molina A, Jackson L, Madhu B, Griffiths J . Noninvasive magnetic resonance spectroscopic pharmacodynamic markers of the choline kinase inhibitor MN58b in human carcinoma models. Cancer Res. 2006; 66(1):427-34. DOI: 10.1158/0008-5472.CAN-05-1338. View