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Published on: November 2, 2013
Strong Stromal Hyaluronan Expression Is Associated with PSA Recurrence in Local Prostate Cancer
S Aaltomaa1, P Lipponen, R Tammi
1Department of Urology, Kuopio University Hospital, Kuopio. Finland. sirpa.aaltomaa@kuh.fi
Urologia Internationalis
|November 22, 2002
Summary
Strong stromal hyaluronan (HA) expression correlates with prostate cancer recurrence and unfavorable prognostic factors like perineural infiltration and seminal vesicle invasion. Further research is needed for definitive conclusions.
Area of Science:
- Oncology
- Biochemistry
Background:
- Hyaluronan (HA) and its receptor CD44 are implicated in tumor growth, migration, and neovascularization.
- CD44 plays a role in cancer cell adhesion and migration.
- Prostate-specific antigen (PSA) recurrence is a key indicator of prostate cancer progression.
Purpose of the Study:
- To investigate the expression of HA and CD44 in prostate cancer (PC).
- To determine the relationship between HA and CD44 expression and prognostic factors.
- To assess the association with PSA recurrence after radical prostatectomy.
Main Methods:
- Studied 77 prostate cancer patients treated with radical prostatectomy.
- Analyzed HA expression using a specific probe and CD44 expression via immunohistochemistry.
- Followed patients for a mean of 4 years to monitor PSA recurrence.
Main Results:
- Strong stromal HA expression was observed in 78% of tumors and correlated with perineural infiltration and capsule invasion.
- CD44 expression was found in 66% of tumors and linked to preoperative PSA levels.
- Strong stromal HA expression, pT classification, seminal vesicle invasion, capsule invasion, and surgical margin invasion predicted PSA recurrence.
Conclusions:
- Strong stromal HA expression is associated with PSA recurrence and adverse prognostic factors in prostate cancer.
- While linked to unfavorable prognosis, the study's follow-up is too short for definitive prognostic conclusions.
- Seminal vesicle infiltration emerged as an independent predictor of PSA recurrence-free survival in multivariate analysis.

