Covid-19 Research

Open Access
Short Communication
OCLC

Artificial Provoking the Apoptosis of Tumoral Cells as Potential Approach in Healing of Malignant Tumors Google Scholar

Read • Cite • Share — permanent Open Access hosting with DOI tracking

Ivan Milosevic*

Volume5-Issue2
Dates: Received: 2024-01-17 | Accepted: 2024-01-29 | Published: 2024-02-01
Pages: 089-091

Abstract

As already known, traditional approaches in healing of many kinds of malignant tumors unfortunatelly still gives bad results. Also, our immune system is not able to respond on malignant tumors in an adequate capacity, because they are growing rapidly and they have pretty developed mechanisms in order to avoid our immune response. Potential answer how to accelerate our immune system and make it more responsive to malignant tumors maybe is hidden in an attempt to make tumoral cells infected by viruses. That way viruses would mark tumoral cells and provoke stronger immune response activating apoptosis of tumoral cells as a final effect.

FullText HTML FullText PDF DOI: 10.37871/jbres1875


Certificate of Publication




Copyright

© 2024 Milosevic I. Distributed under Creative Commons CC-BY 4.0

How to cite this article

Milosevic I. Artifi cial Provoking the Apoptosis of Tumoral Cells as Potential Approach in Healing of Malignant Tumors. J Biomed Res Environ Sci. 2024 Feb 01; 5(2): 089-091. doi: 10.37871/jbres1875, Article ID: JBRES1875, Available at: https:// www.jelsciences.com/articles/jbres1875.pdf


Subject area(s)

References


  1. Abbas AK, Lichtman AH. Immune response against tumors, Basic Immunology. 2007;177-184.
  2. Patic VJ. Immune response to viral infections, Medical Virology. 1995;45-52.
  3. Abul KA, Andrew HL, Jordan SP. Cellular and molecular immunology. W.B. Saunders Company. 2000;406-411.
  4. Guyton AC. Immune system physiology. Medical Physiology. 1996.
  5. Oxford Textbook of Cancer Biology. Francesco Pezzella, Mahvash Tavassoli, David JK, editors; 2019.


Comments


Publish with JBRES — Peer-reviewed, multidisciplinary Open Access with rapid review, DOI, and global visibility.
Double-Blind CrossRef DOI Discoverable