# The dual roles of exosomes in prostate cancer: mechanisms in tumorigenesis and avenues for clinical translation

**Authors:** Mingyun Yu, Dan Zhou, Huijie Wei, Tong Wu, Jiahong Fan, Guanghe Ran, Chong Zhang

PMC · DOI: 10.3389/fimmu.2026.1748272 · Frontiers in Immunology · 2026-02-11

## TL;DR

This paper reviews how exosomes both promote prostate cancer and offer new ways to detect and treat it.

## Contribution

The paper highlights the dual roles of exosomes in prostate cancer progression and their potential for clinical applications.

## Key findings

- Exosomes contribute to tumor growth by aiding metastasis and immune evasion.
- They can be used as non-invasive biomarkers for early diagnosis and treatment monitoring.
- Engineered exosomes show promise as targeted drug delivery vehicles in therapy.

## Abstract

Prostate cancer (PCa) management remains challenged by tumor heterogeneity, unpredictable progression, and limitations in early detection, driving demand for innovative biological insights. As pivotal mediators of intercellular communication, exosomes exhibit dualistic roles in PCa pathogenesis and therapy. While acting as ‘foes’ by facilitating epithelial-mesenchymal transition (EMT), angiogenesis, tumor microenvironment formation, metastasis, immune evasion, and therapy resistance, they concurrently serve as ‘friends’ through their diagnostic and therapeutic potential. Exosome-derived biomarkers enable non-invasive liquid biopsy for early diagnosis, risk stratification, and treatment monitoring. Moreover, engineered exosomes function as targeted drug carriers, delivering precision therapeutics to overcome treatment barriers. This review systematically examines exosomal biogenesis, isolation methodologies, and their bidirectional regulation in PCa progression, while exploring emerging diagnostic and therapeutic applications to advance exosome-mediated precision oncology.

## Linked entities

- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** MYH9 (myosin heavy chain 9) [NCBI Gene 4627] {aka BDPLT6, DFNA17, EPSTS, FTNS, MATINS, MHA}, NKX3-1 (NK3 homeobox 1) [NCBI Gene 4824] {aka BAPX2, NKX3, NKX3.1, NKX3A}, MIR2909 (microRNA 2909) [NCBI Gene 100422969], HK2 (hexokinase 2) [NCBI Gene 3099] {aka HKII, HXK2}, CALM1 (calmodulin 1) [NCBI Gene 801] {aka CALML2, CAM2, CAM3, CAMB, CAMC, CAMI}, MAP3K1 (mitogen-activated protein kinase kinase kinase 1) [NCBI Gene 4214] {aka MAPKKK1, MEKK, MEKK 1, MEKK1, SRXY6}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, MIR574 (microRNA 574) [NCBI Gene 693159] {aka MIR574-3p, MIRN574, hsa-mir-574, mir-574}, MIR1263 (microRNA 1263) [NCBI Gene 100302148] {aka MIRN1263, hsa-mir-1263}, CHAC1 (ChaC glutathione specific gamma-glutamylcyclotransferase 1) [NCBI Gene 79094], MIR1182 (microRNA 1182) [NCBI Gene 100302132] {aka MIRN1182, hsa-mir-1182}, MIR146A (microRNA 146a) [NCBI Gene 406938] {aka MIRN146, MIRN146A, miR-146a, miRNA146A}, CDK6 (cyclin dependent kinase 6) [NCBI Gene 1021] {aka MCPH12, PLSTIRE}, CXCL12 (C-X-C motif chemokine ligand 12) [NCBI Gene 6387] {aka IRH, PBSF, SCYB12, SDF1, TLSF, TPAR1}, PLIN2 (perilipin 2) [NCBI Gene 123] {aka ADFP, ADRP}, CD82 (CD82 molecule) [NCBI Gene 3732] {aka 4F9, C33, GR15, IA4, KAI1, R2}, MIR217 (microRNA 217) [NCBI Gene 406999] {aka MIRN217, mir-217}, CDH1 (cadherin 1) [NCBI Gene 999] {aka Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM}, AKR1C3 (aldo-keto reductase family 1 member C3) [NCBI Gene 8644] {aka DD3, DDX, HA1753, HAKRB, HAKRe, HSD17B5}, ERG (ETS transcription factor ERG) [NCBI Gene 2078] {aka LMPHM14, erg-3, p55}, MIR187 (microRNA 187) [NCBI Gene 406963] {aka MIRN187, miR-187, miRNA187}, GDE1 (glycerophosphodiester phosphodiesterase 1) [NCBI Gene 51573] {aka 363E6.2, MIR16}, S100A9 (S100 calcium binding protein A9) [NCBI Gene 6280] {aka 60B8AG, CAGB, CFAG, CGLB, L1AG, LIAG}, SMAD3 (SMAD family member 3) [NCBI Gene 4088] {aka HSPC193, HsT17436, JV15-2, LDS1C, LDS3, MADH3}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, HDAC1 (histone deacetylase 1) [NCBI Gene 3065] {aka GON-10, HD1, KDAC1, RPD3, RPD3L1}, PGP (phosphoglycolate phosphatase) [NCBI Gene 283871] {aka AUM, G3PP, PGPase}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}, MIR636 (microRNA 636) [NCBI Gene 693221] {aka MIRN636, hsa-mir-636}, PTEN (phosphatase and tensin homolog) [NCBI Gene 5728] {aka 10q23del, BZS, CWS1, DEC, GLM2, MHAM}, ITGA2 (integrin subunit alpha 2) [NCBI Gene 3673] {aka BR, CD49B, FMAIT3, GPIa, HPA-5, VLA-2}, SIRPA (signal regulatory protein alpha) [NCBI Gene 140885] {aka BIT, CD172A, MFR, MYD-1, MYD1, P84}, ABCB1 (ATP binding cassette subfamily B member 1) [NCBI Gene 5243] {aka ABC20, CD243, CLCS, ENPAT, GP170, MDR1}, XCL1 (X-C motif chemokine ligand 1) [NCBI Gene 6375] {aka ATAC, LPTN, LTN, SCM-1, SCM-1a, SCM1}, HSP90AA1 (heat shock protein 90 alpha family class A member 1) [NCBI Gene 3320] {aka EL52, HEL-S-65p, HSP86, HSP89A, HSP90A, HSP90N}, RUNX2 (RUNX family transcription factor 2) [NCBI Gene 860] {aka AML3, CBF-alpha-1, CBFA1, CCD, CCD1, CLCD}, OR51E2 (olfactory receptor family 51 subfamily E member 2) [NCBI Gene 81285] {aka HPRAJ, OR51E3P, OR52A2, PSGR}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, FBXW7 (F-box and WD repeat domain containing 7) [NCBI Gene 55294] {aka AGO, CDC4, DEDHIL, FBW6, FBW7, FBX30}, MIR15A (microRNA 15a) [NCBI Gene 406948] {aka MIRN15A, hsa-mir-15a, miRNA15A, mir-15a}, RELB (RELB proto-oncogene, NF-kB subunit) [NCBI Gene 5971] {aka I-REL, IMD53, IREL, REL-B}, TRIB1 (tribbles pseudokinase 1) [NCBI Gene 10221] {aka C8FW, GIG-2, GIG2, SKIP1, TRB-1, TRB1}, MIR27A (microRNA 27a) [NCBI Gene 407018] {aka MIR27, MIRN27A, mir-27a}, RSU1 (Ras suppressor protein 1) [NCBI Gene 6251] {aka RSP-1}, MIR432 (microRNA 432) [NCBI Gene 574451] {aka MIRN432, hsa-mir-432, mir-432}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, FSD1 (fibronectin type III and SPRY domain containing 1) [NCBI Gene 79187] {aka GLFND, MIR1}, MMP2 (matrix metallopeptidase 2) [NCBI Gene 4313] {aka CLG4, CLG4A, MMP-2, MMP-II, MONA, TBE-1}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}, ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}, SNAI1 (snail family transcriptional repressor 1) [NCBI Gene 6615] {aka SLUGH2, SNA, SNAH, SNAIL, SNAIL1, dJ710H13.1}, KLRC1 (killer cell lectin like receptor C1) [NCBI Gene 3821] {aka CD159A, NKG2, NKG2A}, ENO2 (enolase 2) [NCBI Gene 2026] {aka HEL-S-279, NSE}, CXCR4 (C-X-C motif chemokine receptor 4) [NCBI Gene 7852] {aka CD184, D2S201E, FB22, HM89, HSY3RR, LCR1}, MIR935 (microRNA 935) [NCBI Gene 100126325] {aka MIRN935, hsa-mir-935, mir-935}, MIR215 (microRNA 215) [NCBI Gene 406997] {aka MIRN215, miRNA215, mir-215}, MIR155 (microRNA 155) [NCBI Gene 406947] {aka MIRN155, miRNA155, mir-155}, PCA3 (prostate cancer associated 3) [NCBI Gene 50652] {aka DD3, NCRNA00019, PCAT3, PRUNE2-AS1}, NR0B2 (nuclear receptor subfamily 0 group B member 2) [NCBI Gene 8431] {aka SHP, SHP1}
- **Diseases:** hypoxia (MESH:D000860), prostate tumor (MESH:D011472), brain tumor (MESH:D001932), hyperthermia (MESH:D005334), endotoxin (MESH:D012772), tumorigenesis (MESH:D063646), hypoxic (MESH:D002534), Castration-Resistant Prostate Cancer (MESH:D064129), hormone resistance (MESH:D018382), BPH (MESH:D011470), toxicity (MESH:D064420), prostate adenocarcinoma (MESH:D000230), Cancer Metastasis (MESH:D009369), cardiovascular pathologies (MESH:D002318), Alcohol Abuse (MESH:D000437), PC (MESH:D015324), tumorigenic (MESH:D002471), bone metastases (MESH:D009362), PCa bone metastasis (MESH:D011471), inflammation (MESH:D007249)
- **Chemicals:** ceramide (MESH:D002518), glucose (MESH:D005947), glucosamine (MESH:D005944), DTX (MESH:D000077143), GW4869 (MESH:C468773), taxane (MESH:C080625), PGE2 (MESH:D015232), lactosylceramide (MESH:C009744), lipid (MESH:D008055), Fe (MESH:D007501), steroid (MESH:D013256), GSH (MESH:D005978), m6A (MESH:C005955), ATP (MESH:D000255), enzalutamide (MESH:C540278), Venofer (MESH:D000077605), fatty acid (MESH:D005227), carbon (MESH:D002244), phosphatidylserine (MESH:D010718), serine (MESH:D012694), paclitaxel (MESH:D017239), lactate (MESH:D019344), oxygen (MESH:D010100), DOX (MESH:D004317), HSA@DOX (-), cisplatin (MESH:D002945)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** PC-3M-luc — Homo sapiens (Human), Prostate carcinoma, Cancer cell line (CVCL_5J25), DU145 — Homo sapiens (Human), Prostate carcinoma, Cancer cell line (CVCL_0105), RWPE-1 — Homo sapiens (Human), Transformed cell line (CVCL_3791), PC-3 — Homo sapiens (Human), Prostate carcinoma, Cancer cell line (CVCL_0035), PWR-1E — Homo sapiens (Human), Transformed cell line (CVCL_3775), LNCaP — Homo sapiens (Human), Prostate carcinoma, Cancer cell line (CVCL_0395), 22Rv1 — Homo sapiens (Human), Prostate carcinoma, Cancer cell line (CVCL_1045), NCI-H660 — Homo sapiens (Human), Prostate small cell carcinoma, Cancer cell line (CVCL_1576), C42B — Homo sapiens (Human), Floor of mouth squamous cell carcinoma, Cancer cell line (CVCL_WI17), C4-2B — Homo sapiens (Human), Prostate carcinoma, Cancer cell line (CVCL_4784)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12932536/full.md

## References

193 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932536/full.md

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Source: https://tomesphere.com/paper/PMC12932536