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BMC Cancer. 2015 Oct 22;15:762. doi: 10.1186/s12885-015-1718-7.

Regulation of cellular sphingosine-1-phosphate by sphingosine kinase 1 and sphingosine-1-phopshate lyase determines chemotherapy resistance in gastroesophageal cancer.

Author information

1
School of Medicine and Dentistry, University of Aberdeen, Aberdeen Royal Infirmary, Foresterhill Healthcare Campus, Foresterhill, Aberdeen, AB25 2ZG, Scotland, UK.
2
Department of Pathology, University of Aberdeen, Aberdeen Royal Infirmary, Foresterhill Healthcare Campus, Foresterhill, Aberdeen, AB25 2ZG, Scotland, UK.
3
Department of Pathology, Maastricht University Medical Center, Maastricht, The Netherlands.
4
Cancer Science Institute of Singapore National University of Singapore, Singapore, Singapore.
5
Department of Gastroenterology, University of Aberdeen, Aberdeen Royal Infirmary, Foresterhill Healthcare Campus, Foresterhill, Aberdeen, AB25 2ZG, Scotland, United Kingdom.
6
Department of Oncology, University of Aberdeen, Aberdeen Royal Infirmary, Foresterhill Healthcare Campus, Foresterhill, Aberdeen, AB25 2ZG, Scotland, UK.
7
Department of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC, USA.
8
Division of Cancer Research, School of Medicine, University of Dundee, Mailbox 4, Level 7 Ninewells Hospital and Medical School, Dundee, DD1 9SY, Scotland, UK. r.petty@dundee.ac.uk.

Abstract

BACKGROUND:

Resistance to chemotherapy is common in gastroesophageal cancer. Mechanisms of resistance are incompletely characterised and there are no predictive biomarkers in clinical practice for cytotoxic drugs. We used new cell line models to characterise novel chemotherapy resistance mechanisms and validated them in tumour specimens to identify new targets and biomarkers for gastroesophageal cancer.

METHODS:

Cell lines were selected for resistance to oxaliplatin, cisplatin and docetaxel and gene expression examined using Affymetrix Exon 1.0 ST arrays. Leads were validated by qRT-PCR and HPLC of tumour metabolites. Protein expression and pharmacological inhibition of lead target SPHK1 was evaluated in independent cell lines, and by immunohistochemistry in gastroesophageal cancer patients.

RESULTS:

Genes with differential expression in drug resistant cell lines compared to the parental cell line they were derived from, were identified for each drug resistant cell line. Biological pathway analysis of these gene lists, identified over-represented pathways, and only 3 pathways - lysosome, sphingolipid metabolism and p53 signalling- were identified as over-represented in these lists for all three cytotoxic drugs investigated. The majority of genes differentially expressed in chemoresistant cell lines from these pathways, were involved in metabolism of glycosphingolipids and sphingolipids in lysosomal compartments suggesting that sphingolipids might be important mediators of cytotoxic drug resistance in gastroeosphageal cancers . On further investigation, we found that drug resistance (IC50) was correlated with increased sphingosine kinase 1(SPHK1) mRNA and also with decreased sphingosine-1-phosphate lysase 1(SGPL1) mRNA. SPHK1 and SGPL1 gene expression were inversely correlated. SPHK1:SGPL1 ratio correlated with increased cellular sphingosine-1-phosphate (S1P), and S1P correlated with drug resistance (IC50). High SPHK1 protein correlated with resistance to cisplatin (IC50) in an independent gastric cancer cell line panel and with survival of patients treated with chemotherapy prior to surgery but not in patients treated with surgery alone. Safingol a SPHK1 inhibitor, was cytotoxic as a single agent and acted synergistically with cisplatin in gastric cancer cell lines.

CONCLUSION:

Agents that inhibit SPHK1 or S1P could overcome cytotoxic drug resistance in gastroesophageal cancer. There are several agents in early phase human trials including Safingol that could be combined with chemotherapy or used in patients progressing after chemotherapy.

PMID:
26493335
PMCID:
PMC4618539
DOI:
10.1186/s12885-015-1718-7
[Indexed for MEDLINE]
Free PMC Article

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