Targeted Mechanisms for Proliferation Inhibition and Selective Apoptosis Induction in Cancer Therapy

Abstract:Traditional cancer therapies often suffer from systemic toxicity and lack of selectivity toward malignant cells. Developing targeted therapeutic approaches that selectively eliminate cancer cells while preserving healthy tissues remains a critical challenge in oncology. This study proposes a novel conceptual strategy focusing on the targeted disruption of key cellular proliferation pathways and the selective induction of apoptosis in cancer cells. The mechanism leverages specific biochemical pathways designed to minimize off-target cytotoxicity. Preliminary theoretical models and in vitro frameworks demonstrate enhanced selectivity against malignant cell populations with significantly reduced collateral damage to non-cancerous cells. This approach provides a promising framework for non-toxic targeted oncological therapy and serves as a viable foundation for subsequent preclinical and clinical evaluations..

Authors

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2026-10-27
DOI
https://doi.org/10.5281/zenodo.23683869
Primary Topic
Cancer-related Molecular Pathways
Type
article
Field-Weighted Citation Impact
0.00
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article

Targeted Mechanisms for Proliferation Inhibition and Selective Apoptosis Induction in Cancer Therapy

Samane Saeedi
1 links
Zenodo (CERN European Organization for Nuclear Research)
Cancer-related Molecular Pathways
article

Targeted Mechanisms for Proliferation Inhibition and Selective Apoptosis Induction in Cancer Therapy

Samane Saeedi
article en

Abstract

Abstract:Traditional cancer therapies often suffer from systemic toxicity and lack of selectivity toward malignant cells. Developing targeted therapeutic approaches that selectively eliminate cancer cells while preserving healthy tissues remains a critical challenge in oncology. This study proposes a novel conceptual strategy focusing on the targeted disruption of key cellular proliferation pathways and the selective induction of apoptosis in cancer cells. The mechanism leverages specific biochemical pathways designed to minimize off-target cytotoxicity. Preliminary theoretical models and in vitro frameworks demonstrate enhanced selectivity against malignant cell populations with significantly reduced collateral damage to non-cancerous cells. This approach provides a promising framework for non-toxic targeted oncological therapy and serves as a viable foundation for subsequent preclinical and clinical evaluations..

Zenodo (CERN European Organization for Nuclear Research)
Good health and well-being
Openalex Percentile: Top 16%
Cancer-related Molecular Pathways
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