# Detection of bimodal survivin expressions in canine cancer types by flow cytometry compared to immunohistochemistry

**Authors:** Shohei Tsumoto, Kyoichi Tamura, Yuta Nakazawa, Michio Fujita, Kozo Ohkusu-Tsukada

PMC · DOI: 10.3389/fvets.2025.1552415 · Frontiers in Veterinary Science · 2025-03-27

## TL;DR

This study introduces a new flow cytometry method to detect survivin in canine cancer cells using needle biopsies, avoiding anesthesia and enabling faster diagnosis.

## Contribution

A novel FCM method is proposed to rapidly detect survivin expression and localization in canine cancer samples using needle biopsies.

## Key findings

- FCM detected bimodal survivin expression patterns in canine and murine cancer cell lines.
- Survivin localization (nuclear-cytosol vs. cytosol alone) was distinguishable via FCM fluorescence intensity.
- Needle biopsy samples enabled survivin detection in clinical canine cancer cases without anesthesia.

## Abstract

Animal practice requires both convenience for the owner and risk management for the animal's health. Deterioration due to cancer may associate with poor prognosis under general anesthesia, which need to partial excision for pathological diagnosis. This study aimed to establish rapidly detecting the expression of survivin antigens for cancer vaccines or molecular targeted therapies via flow cytometry (FCM) using the intracellular staining method in tumor samples obtained via needle biopsy without anesthesia. Therefore, survivin expression patterns in each cell lines of canine melanomas, a murine mast cell tumor, a murine colon carcinoma, and a murine melanoma was analyzed by FCM and immunofluorescence microscopy, and compared with immunohistochemical analysis and western blot method. Interestingly, FCM results of the bimodal expression pattern of survivin were suggested to reflect the high fluorescence intensity of its nuclear–cytosol localization and the weak fluorescence intensity of its cytosol alone localization. In a case of canine cancer disease, it was confirmed that survivin expression patterns can be detected via FCM using needle biopsy samples in actual clinical settings. In this study, a novel method via FCM was proposed to quickly determine also survivin localization not only whether the survivin is expressed in cancer cells. The application of cancer vaccine or chemical therapy via this technology can be expected to contribute to improved animal care due to the “one-day first program,” which has been proposed in convenience for owners.

## Linked entities

- **Genes:** birc5a (baculoviral IAP repeat containing 5a) [NCBI Gene 373110]
- **Diseases:** mast cell tumor (MONDO:0002724), colon carcinoma (MONDO:0002032)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** BIRC5 (baculoviral IAP repeat containing 5) [NCBI Gene 442936]
- **Diseases:** colon carcinoma (MESH:D003110), mast cell tumor (MESH:D007946), cancer (MESH:D009369), Deterioration (MESH:D000075902), melanoma (MESH:D008545)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Canis lupus familiaris (dog, subspecies) [taxon 9615]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11984292/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC11984292/full.md

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Source: https://tomesphere.com/paper/PMC11984292