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Accelerated cancer aggressiveness by viral oncomodulation: New targets and newer natural treatments for cancer control and treatment

An infectious etiology for a number of cancers has been entertained for over 100 years and modern studies have confirmed that a number of viruses are linked to cancer induction. While a large number of viruses have been demonstrated in a number of types of cancers, most such findings have been dismi...

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Autor principal: Blaylock, Russell L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826277/
https://www.ncbi.nlm.nih.gov/pubmed/31768279
http://dx.doi.org/10.25259/SNI_361_2019
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author Blaylock, Russell L.
author_facet Blaylock, Russell L.
author_sort Blaylock, Russell L.
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description An infectious etiology for a number of cancers has been entertained for over 100 years and modern studies have confirmed that a number of viruses are linked to cancer induction. While a large number of viruses have been demonstrated in a number of types of cancers, most such findings have been dismissed in the past as opportunistic infections, especially with persistent viruses with high rates of infectivity of the world’s populations. More recent studies have clearly shown that while not definitely causing these cancers, these viruses appear capable of affecting the biology of these tumors in such a way as to make them more aggressive and more resistant to conventional treatments. The term oncomodulatory viruses has been used to describe this phenomenon. A number of recent studies have shown a growing number of ways these oncomodulatory viruses can alter the pathology of these tumors by affecting cell-signaling, cell metabolism, apoptosis mechanisms, cell-cell communication, inflammation, antitumor immunity suppression, and angiogenesis. We are also learning that much of the behavior of tumors depends on cancer stem cells and stromal cells within the tumor microenvironment, which participate in extensive, dynamic crosstalk known to affect tumor behavior. Cancer stem cells have been found to be particularly susceptible to infection by human cytomegalovirus. In a number of studies, it has been shown that while only a select number of cells are actually infected with the virus, numerous viral proteins are released into cancer and stromal cells in the microenvironment and these viral proteins are known to affect tumor behavior and aggressiveness.
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spelling pubmed-68262772019-11-25 Accelerated cancer aggressiveness by viral oncomodulation: New targets and newer natural treatments for cancer control and treatment Blaylock, Russell L. Surg Neurol Int Review Article An infectious etiology for a number of cancers has been entertained for over 100 years and modern studies have confirmed that a number of viruses are linked to cancer induction. While a large number of viruses have been demonstrated in a number of types of cancers, most such findings have been dismissed in the past as opportunistic infections, especially with persistent viruses with high rates of infectivity of the world’s populations. More recent studies have clearly shown that while not definitely causing these cancers, these viruses appear capable of affecting the biology of these tumors in such a way as to make them more aggressive and more resistant to conventional treatments. The term oncomodulatory viruses has been used to describe this phenomenon. A number of recent studies have shown a growing number of ways these oncomodulatory viruses can alter the pathology of these tumors by affecting cell-signaling, cell metabolism, apoptosis mechanisms, cell-cell communication, inflammation, antitumor immunity suppression, and angiogenesis. We are also learning that much of the behavior of tumors depends on cancer stem cells and stromal cells within the tumor microenvironment, which participate in extensive, dynamic crosstalk known to affect tumor behavior. Cancer stem cells have been found to be particularly susceptible to infection by human cytomegalovirus. In a number of studies, it has been shown that while only a select number of cells are actually infected with the virus, numerous viral proteins are released into cancer and stromal cells in the microenvironment and these viral proteins are known to affect tumor behavior and aggressiveness. Scientific Scholar 2019-10-11 /pmc/articles/PMC6826277/ /pubmed/31768279 http://dx.doi.org/10.25259/SNI_361_2019 Text en Copyright: © 2019 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Review Article
Blaylock, Russell L.
Accelerated cancer aggressiveness by viral oncomodulation: New targets and newer natural treatments for cancer control and treatment
title Accelerated cancer aggressiveness by viral oncomodulation: New targets and newer natural treatments for cancer control and treatment
title_full Accelerated cancer aggressiveness by viral oncomodulation: New targets and newer natural treatments for cancer control and treatment
title_fullStr Accelerated cancer aggressiveness by viral oncomodulation: New targets and newer natural treatments for cancer control and treatment
title_full_unstemmed Accelerated cancer aggressiveness by viral oncomodulation: New targets and newer natural treatments for cancer control and treatment
title_short Accelerated cancer aggressiveness by viral oncomodulation: New targets and newer natural treatments for cancer control and treatment
title_sort accelerated cancer aggressiveness by viral oncomodulation: new targets and newer natural treatments for cancer control and treatment
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826277/
https://www.ncbi.nlm.nih.gov/pubmed/31768279
http://dx.doi.org/10.25259/SNI_361_2019
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