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Innovating Cancer Treatment Through Cell Cycle, Telomerase, Angiogenesis, and Metastasis.

Authors :
Yousefi, Tooba
Mohammadi Jobani, Bahareh
Taebi, Reyhaneh
Qujeq, Durdi
Source :
DNA & Cell Biology. Sep2024, Vol. 43 Issue 9, p438-451. 14p.
Publication Year :
2024

Abstract

Cancer remains a formidable challenge in the field of medicine, necessitating innovative therapeutic strategies to combat its relentless progression. The cell cycle, a tightly regulated process governing cell growth and division, plays a pivotal role in cancer development. Dysregulation of the cell cycle allows cancer cells to proliferate uncontrollably. Therapeutic interventions designed to disrupt the cell cycle offer promise in restraining tumor growth and progression. Telomerase, an enzyme responsible for maintaining telomere length, is often overactive in cancer cells, conferring them with immortality. Targeting telomerase presents an opportunity to limit the replicative potential of cancer cells and hinder tumor growth. Angiogenesis, the formation of new blood vessels, is essential for tumor growth and metastasis. Strategies aimed at inhibiting angiogenesis seek to deprive tumors of their vital blood supply, thereby impeding their progression. Metastasis, the spread of cancer cells from the primary tumor to distant sites, is a major challenge in cancer therapy. Research efforts are focused on understanding the underlying mechanisms of metastasis and developing interventions to disrupt this deadly process. This review provides a glimpse into the multifaceted approach to cancer therapy, addressing critical aspects of cancer biology—cell cycle regulation, telomerase activity, angiogenesis, and metastasis. Through ongoing research and innovative strategies, the field of oncology continues to advance, offering new hope for improved treatment outcomes and enhanced quality of life for cancer patients. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10445498
Volume :
43
Issue :
9
Database :
Academic Search Index
Journal :
DNA & Cell Biology
Publication Type :
Academic Journal
Accession number :
179663300
Full Text :
https://doi.org/10.1089/dna.2024.0109