# Multi-Omics Analysis of the Anoikis Gene CASP8 in Prostate Cancer and Biochemical Recurrence (BCR)

**Authors:** Shan Huang, Hang Yin

PMC · DOI: 10.3390/biomedicines13030661 · Biomedicines · 2025-03-07

## TL;DR

This study explores the role of the CASP8 gene in prostate cancer and its potential as a biomarker for predicting biochemical recurrence.

## Contribution

The study identifies CASP8 as a potential biomarker and constructs a four-gene model for predicting prostate cancer recurrence.

## Key findings

- High-risk prostate cancer patients showed higher tumor purity and BCR rates.
- CASP8 was found to increase prostate cancer risk according to SMR analysis.
- A four-gene model achieved a 5-year AUC of 0.713 for predicting BCR.

## Abstract

Background: Prostate cancer, as an androgen-dependent malignant tumor in older men, has attracted the attention of a wide range of clinicians. BCR remains a significant challenge following early prostate cancer treatment. Methods: The specific expression pattern of the Anoikis gene set in prostate cancer cells was first explored by single-cell and spatial transcriptomics analysis. Genes causally associated with prostate cancer were screened using Summary-data-based Mendelian Randomization (SMR). Subsequently, we explored the role and mechanism of CASP8 in prostate cancer cells and defined a new cell type: the CASP8 T cell. We constructed a prediction model that can better predict the BCR of prostate cancer, and explored the differences in various aspects of clinical subgroups, tumor microenvironments, immune checkpoints, drug sensitivities, and tumor-immune circulations between high- and low-risk groups. The results of SMR analysis indicated that CASP8 could increase the risk of prostate cancer. Based on the differential genes of CASP8-positive and -negative T cells, we constructed a four-gene prognostic model with a 5-year AUC of 0.713. Results: The results revealed that high-risk prostate cancer BCR patients had various characteristics such as higher tumor purity, higher BCR rate, downregulated SIRPA immune checkpoints, and unique drug sensitivity. Conclusions: In summary, CASP8 may be a potential biomarker for prostate cancer.

## Linked entities

- **Genes:** CASP8 (caspase 8) [NCBI Gene 841], SIRPA (signal regulatory protein alpha) [NCBI Gene 140885]
- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** CASP8 (caspase 8) [NCBI Gene 841] {aka ALPS2B, CAP4, Casp-8, FLICE, MACH, MCH5}, SIRPA (signal regulatory protein alpha) [NCBI Gene 140885] {aka BIT, CD172A, MFR, MYD-1, MYD1, P84}
- **Diseases:** malignant tumor (MESH:D009369), Prostate Cancer (MESH:D011471)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11939882/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11939882/full.md

## References

64 references — full list in the complete paper: https://tomesphere.com/paper/PMC11939882/full.md

---
Source: https://tomesphere.com/paper/PMC11939882