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Updated: Jul 6, 2026

miRNA Expression Analyses in Prostate Cancer Clinical Tissues
Published on: September 8, 2015
Genetic changes and DNA damage responses in the prostate
Taija M Kiviharju-Af Hällström1, Marikki Laiho
1Molecular Cancer Biology Program, Biomedicum Helsinki and Haartman Institute, University of Helsinki, Helsinki, Finland.
Abstract:
The integrity of genomic DNA is challenged by genotoxic stress originating during normal cellular metabolism or by external insults. Cellular responses to DNA damage involve elegant checkpoint cascades enforcing cell cycle arrest, damage repair, apoptosis or cellular senescence. The loss or alterations of genes involved in the damage response pathways have been reported in many cancer susceptibility syndromes and in sporadic tumors. Furthermore, this surveillance pathway is activated during early tumourigenesis presumably due to uncontrolled replicative cycles and has been recognized as one of the main barriers against the development of cancer. This review discusses the relevance of prostatic epithelial cells in prostate tumourigenesis and highlights common molecular changes associated with prostate cancer. Furthermore, DNA damage responses of primary cultures of human prostatic epithelial cells and fresh human prostate tissues are discussed providing evidence for alterations in crucial DNA damage checkpoint molecules. New insights connecting prostate tumourigenesis to alterations and defects in the pathways maintaining genomic integrity will be discussed.
Insights
Genomic DNA integrity is crucial for preventing cancer. This review explores how DNA damage response defects in prostate cells contribute to prostate cancer development.
Area of Science:
- Molecular Biology
- Genetics
- Oncology
Background:
- Genomic DNA integrity is constantly challenged by metabolic byproducts and external factors.
- Cellular responses to DNA damage include cell cycle arrest, repair, apoptosis, and senescence.
- Alterations in DNA damage response genes are linked to cancer susceptibility and sporadic tumors.
Purpose of the Study:
- To review the role of prostatic epithelial cells in prostate tumorigenesis.
- To highlight molecular alterations common in prostate cancer.
- To discuss DNA damage responses in human prostate cells and tissues.
Main Methods:
- Review of existing literature on DNA damage response pathways.
- Analysis of molecular changes in prostate cancer.
- Examination of DNA damage responses in primary human prostate epithelial cells and tissues.
Main Results:
- Prostatic epithelial cells play a significant role in prostate tumorigenesis.
- Common molecular changes in prostate cancer involve DNA damage response pathways.
- Evidence suggests alterations in key DNA damage checkpoint molecules in human prostate cells and tissues.
Conclusions:
- Defects in DNA damage response pathways are implicated in prostate cancer.
- Maintaining genomic integrity is a critical barrier against cancer development.
- Further research into these pathways may offer new therapeutic strategies for prostate cancer.
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