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Updated: May 11, 2026

Transmitochondrial Cybrid Generation Using Cancer Cell Lines
Published on: March 17, 2023
Cancer therapy: Targeting mitochondria and other sub-cellular organelles
Obinna C Ubah, Heather M Wallace1
1Division of Applied Medicine and Therapeutics, School of Medicine and Dentistry, University of Aberdeen, Aberdeen AB25 2ZD, UK. h.m.wallace@abdn.ac.uk.
Abstract:
Tumour cell death is required for the clearance of malignant cells and is a vital part of the mechanism of natural tumour suppression. Cancer cells, having acquired multiple deregulated pathways involving several cellular oragenelles, are capable of disrupting these normally finely tuned processes thereby evading both physiological and therapeutic intervention. Although current available data indicate the dependence of successful tumour cell clearance on classical apoptotic pathways (intrinsic and/or extrinsic pathways), there is now evidence suggesting that alternative apoptotic and non-apoptotic pathways may effectively contribute to tumour cell death. The mitochondria, proteasomes, endoplasmic reticulum, Golgi apparatus, lysosomes and lysosome-related organelles of tumour cells exhibit a number of deregulations which have been identified as potential druggable targets for successful rational drug design and therapy. In this review, we summarise the roles of these cellular organelles in tumour initiation and establishment as well as current trends in development of agents that target deregulations in these organelles.
Insights
Tumour cell death, crucial for tumour suppression, can be induced via classical apoptosis or alternative pathways. Targeting deregulated organelles like mitochondria offers new therapeutic strategies for cancer.
Area of Science:
- Oncology
- Cell Biology
- Molecular Biology
Background:
- Tumour cell death is essential for natural tumour suppression.
- Cancer cells evade cell death through deregulated pathways involving cellular organelles.
- While classical apoptosis is known, alternative and non-apoptotic pathways also contribute to tumour cell death.
Purpose of the Study:
- To review the role of cellular organelles in tumour initiation and progression.
- To explore alternative and non-apoptotic pathways in tumour cell death.
- To summarize current drug development targeting deregulated organelles in cancer.
Main Methods:
- Literature review of scientific publications.
- Analysis of data on tumour cell death mechanisms.
- Summary of current therapeutic strategies targeting cellular organelles.
Main Results:
- Deregulated organelles (mitochondria, ER, Golgi, lysosomes) are implicated in tumourigenesis.
- Alternative apoptotic and non-apoptotic pathways contribute to tumour cell death.
- Organelle dysregulations present druggable targets for cancer therapy.
Conclusions:
- Targeting specific organelle dysfunctions represents a promising avenue for rational cancer drug design.
- Understanding diverse cell death pathways enhances therapeutic intervention strategies.
- Further research into organelle-targeted therapies is warranted.
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