# EIF2S1 in Urinary Extracellular Vesicles as a Novel Diagnostic Marker for Bladder Cancer

**Authors:** Eisuke Tomiyama, Kazutoshi Fujita, Kyosuke Matsuzaki, Ryohei Narumi, Makoto Matsushita, Yujiro Hayashi, Mamoru Hashimoto, Taigo Kato, Koji Hatano, Atsunari Kawashima, Takafumi Minami, Tetsuya Takao, Shingo Takada, Hirotsugu Uemura, Jun Adachi, Takeshi Tomonaga, Norio Nonomura

PMC · DOI: 10.1002/cam4.70964 · Cancer Medicine · 2025-05-14

## TL;DR

This study identifies EV-EIF2S1 in urinary extracellular vesicles as a promising new diagnostic marker for bladder cancer.

## Contribution

EV-EIF2S1 is newly identified as a diagnostic marker for bladder cancer with strong functional relevance.

## Key findings

- EV-EIF2S1 showed high diagnostic performance with an AUC of 0.83 for bladder cancer detection.
- EV-EIF2S1 effectively distinguished bladder cancer from non-cancer hematuria with an AUC of 0.92.
- Knockdown of EIF2S1 inhibited bladder cancer cell growth and induced apoptosis.

## Abstract

Urinary extracellular vesicles (uEVs), directly secreted from bladder cancer (BCa) cells, harbor potential for biomarker discovery.

We performed proteomic analysis to explore and validate uEV‐based diagnostic markers for BCa, with a focus on cytoplasmic EV proteins. Among the 1960 proteins identified by shotgun proteomics (tandem mass tag‐labeled liquid chromatography–tandem mass spectrometry [LC–MS/MS]) of uEVs from seven patients with BCa and four healthy individuals, 17 cytoplasmic EV proteins were significantly elevated in the patients' urine (fold change > 1.5; p < 0.05). These 17 proteins were subsequently validated using targeted proteomics (selected reaction monitoring/multiple reaction monitoring) using urine samples from 49 and 48 patients with and without BCa, respectively, including those with non‐BCa hematuria.

Ten measurable EV proteins remained significantly elevated in the urine of patients with BCa, with EV‐EIF2S1 demonstrating the best diagnostic performance (area under the receiver operating characteristic [ROC] curve [AUC] [ROCAUC]: 0.83). Additionally, EV‐EIF2S1 distinguished patients with BCa from those without BCa and hematuria in a suitable manner (ROCAUC: 0.92). Functional analysis of EIF2S1 in the BCa cell lines (T24 and 5637) showed that EIF2S1 knockdown markedly inhibited cell proliferation and induced cell cycle arrest and apoptosis, suggesting its essentiality for BCa cell growth and survival.

This study identified EV‐EIF2S1 as a novel, uEV‐based BCa diagnostic marker and demonstrated its functional significance in BCa cell growth and survival.

We conducted a proteomic analysis of urinary extracellular vesicles (uEVs) to identify and validate new diagnostic markers for bladder cancer. Focusing on cytoplasmic EV proteins, we discovered EV‐EIF2S1 as a novel marker and demonstrated its crucial role in the growth and survival of bladder cancer.

## Linked entities

- **Genes:** EIF2S1 (eukaryotic translation initiation factor 2 subunit alpha) [NCBI Gene 1965]
- **Diseases:** bladder cancer (MONDO:0004986)

## Full-text entities

- **Genes:** EIF2S1 (eukaryotic translation initiation factor 2 subunit alpha) [NCBI Gene 1965] {aka EIF-2, EIF-2A, EIF-2alpha, EIF2, EIF2A}
- **Diseases:** hematuria (MESH:D006417), BCa (MESH:D001749)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** 5637 — Homo sapiens (Human), Bladder carcinoma, Cancer cell line (CVCL_0126), T24 — Homo sapiens (Human), Bladder carcinoma, Cancer cell line (CVCL_0554), BCa — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_S780)

## Full text

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## Figures

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## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12076193/full.md

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Source: https://tomesphere.com/paper/PMC12076193