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Updated: Feb 8, 2026

Isolation of Cancer Stem Cells From Human Prostate Cancer Samples
Published on: March 14, 2014
High ANXA7 Potentiates Eucalyptol Toxicity in Hormone-refractory Prostate Cancer
Ximena Leighton1, Alakesh Bera1, Ofer Eidelman1
1Department of Anatomy, Physiology, and Genetics, and Institute for Molecular Medicine, Uniformed Services University School of Medicine (USUHS), Bethesda, MD, U.S.A.
Background/Aim:
Our studies showed that ANXA7 is a novel tumor suppressor gene that is lost in various aggressive forms of prostate cancer. However, little is known about the role of ANXA7 in the anticancer drug treatment towards different cancers.
Materials And Methods:
The expression of ANXA7 was measured in the 60 cancer cell lines of the NCI-60 ADS project and correlated with the enhanced sensitivity to over 30,000 natural and synthetic compounds.
Results:
Eucalyptol showed a high positive correlation with ANXA7 expression and castration-resistant prostate cancer cell death occurred very effectively in response to the combination of eucalyptol and overexpressed wt-ANXA7 than either agent alone. The synergistic effects of ANXA7 and eucalyptol resulted in concordant changes in gene expression profiles particularly of Ras family members, MDM4, NF-ĸB and VEGF.
Conclusion:
Overexpression of ANXA7 enhances eucalyptol cytotoxicity in prostate cancer cell lines.
Insights
Overexpressing the ANXA7 tumor suppressor gene enhances eucalyptol
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Annexin A7 (ANXA7) functions as a tumor suppressor gene.
- ANXA7 is frequently lost in aggressive prostate cancers.
- The role of ANXA7 in cancer drug sensitivity remains largely unexplored.
Purpose of the Study:
- To investigate the role of ANXA7 in anticancer drug treatment.
- To explore the correlation between ANXA7 expression and sensitivity to various compounds.
- To determine if ANXA7 influences prostate cancer cell response to eucalyptol.
Main Methods:
- Measured ANXA7 expression across 60 cancer cell lines (NCI-60 ADS).
- Correlated ANXA7 levels with sensitivity to over 30,000 natural and synthetic compounds.
- Investigated the effects of ANXA7 overexpression combined with eucalyptol on prostate cancer cells.
Main Results:
- Eucalyptol demonstrated a strong positive correlation with ANXA7 expression.
- Overexpressing ANXA7 significantly enhanced eucalyptol-induced cell death in castration-resistant prostate cancer.
- Synergistic effects were observed, impacting gene expression profiles including Ras family, MDM4, NF-κB, and VEGF.
Conclusions:
- ANXA7 overexpression potentiates eucalyptol's cytotoxic effects in prostate cancer.
- This suggests a potential therapeutic strategy combining ANXA7 modulation with eucalyptol treatment.
- ANXA7 and eucalyptol exhibit synergistic anticancer activity through specific molecular pathways.
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