# Identification of Sphingosine Kinase 1 as a Novel Protein Regulated by High Molecular Weight Hyaluronan in Ovarian Cancer

**Authors:** Zoe K. Price, Noor A. Lokman, Jessica Morrison, Sisanda N. Mhlanga, Mai Sugiyama, Yoshihiro Koya, Lorena T. Davies, Stuart M. Pitson, Martin K. Oehler, Melissa R. Pitman, Masato Yoshihara, Hiroaki Kajiyama, Carmela Ricciardelli

PMC · DOI: 10.1111/jcmm.70574 · Journal of Cellular and Molecular Medicine · 2025-05-12

## TL;DR

This study identifies SPHK1 as a new protein regulated by high molecular weight hyaluronan in ovarian cancer, suggesting it could be a promising therapeutic target.

## Contribution

The study reveals SPHK1 as a novel protein regulated by high molecular weight hyaluronan in ovarian cancer.

## Key findings

- SPHK1 expression is significantly higher in ovarian cancer compared to normal tissues.
- High SPHK1 levels are linked to metastasis, recurrence, and poor patient outcomes in ovarian cancer.
- 4-Methylumbelliferone inhibits SPHK1 expression in ovarian cancer cells and patient tissues.

## Abstract

The effects of hyaluronan (HA) in cancer are widely studied; however, the role of different molecular weight HA is poorly understood. Identifying novel proteins regulated by different molecular weight HA may highlight novel therapeutic targets. Proteomics analysis was performed to identify novel proteins regulated by different molecular weight HA (27, 183 and 1000 kDa) in ES‐2 ovarian cancer cells over‐expressing Notch3 intra‐cellular domain. Our analyses identified sphingosine kinase 1 (SPHK1), a novel protein regulated by 183‐ and 1000‐kDa HA. Utilising online databases and high‐grade serous ovarian cancer (HGSOC) patient tissue microarray cohorts, we assessed the relationship between SPHK1 expression and ovarian cancer metastasis, recurrence and patient outcome. We assessed the effects of the HA synthesis inhibitor 4‐methylumbelliferone (4‐MU) on SPHK1 expression in ovarian cancer cells and HGSOC patient tissues using ex vivo tissue explant assays. SPHK1 was significantly increased in ovarian cancer compared to normal tissues, elevated in metastatic and recurrent HGSOC tissues and associated with poor patient outcome. 4‐MU significantly inhibited SPHK1 expression in ovarian cancer cells (ES‐2, CaOV3 and A2780) and HGSOC patient tissues. This study highlights a link between HA and SPHK1 expression in ovarian cancer. Our findings confirm an adverse effect on ovarian cancer prognosis. SPHK1 constitutes a novel promising target against ovarian cancer that warrants further investigation.

## Linked entities

- **Genes:** SPHK1 (sphingosine kinase 1) [NCBI Gene 8877], NOTCH3 (notch receptor 3) [NCBI Gene 4854]
- **Proteins:** SPHK1 (sphingosine kinase 1)
- **Chemicals:** 4-methylumbelliferone (PubChem CID 5280567)
- **Diseases:** ovarian cancer (MONDO:0005140)

## Full-text entities

- **Genes:** SPHK1 (sphingosine kinase 1) [NCBI Gene 8877] {aka SPHK}, NOTCH3 (notch receptor 3) [NCBI Gene 4854] {aka CADASIL, CADASIL1, CARASIL1, CASIL, FPLD1, IMF2}
- **Diseases:** cancer (MESH:D009369), HGSOC (MESH:D010051)
- **Chemicals:** 4-MU (MESH:D006923), HA (MESH:D006820)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** CaOV3 — Homo sapiens (Human), High grade ovarian serous adenocarcinoma, Cancer cell line (CVCL_0201), ES-2 — Homo sapiens (Human), Embryonic stem cell (CVCL_C769), A2780 — Homo sapiens (Human), Ovarian endometrioid adenocarcinoma, Cancer cell line (CVCL_0134)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12069020/full.md

## References

59 references — full list in the complete paper: https://tomesphere.com/paper/PMC12069020/full.md

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Source: https://tomesphere.com/paper/PMC12069020