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Synopsis: Special Issue on 'Disruption of signaling homeostasis induced crosstalk in the carcinogenesis paradigm Epistemology of the origin of cancer'
- Source :
- 4 open, Vol 2, p 28 (2019)
- Publication Year :
- 2019
- Publisher :
- EDP Sciences, 2019.
-
Abstract
- It is increasingly evident that carcinogenesis, in the vast majority of cancers, cannot be explained simply through an accumulation of somatic mutations, or epigenetics, the stem cell theory, or the Warburg effect. Here, decades of thinking based on incorrect assumptions has resulted in an incorrect hypothesis on the origin of cancer. Many papers studying DNA, genetics, RNA, miRNA, proteomics, and epigenetics have increased our understanding of biology. Our paradigm, though more complex, is more reliable and plausible. It states that cancer originates from a disruption of homeostasis. This essential biological phenomenon, homeostasis, maintains the interrelationships of various signaling pathways and induced crosstalk which modify cellular functions together with the interactions of surrounding cells and structures such that the equilibrium lies towards the optimal health of the organism. This Special Issue “Disruption of signaling homeostasis induced crosstalk in the carcinogenesis paradigm Epistemology of the origin of cancer” provides compelling evidence that carcinogenesis is explained by a six-step sequence of events for the vast majority of cancers. These six steps include, (1) a pathogenic stimulus followed by (2) chronic inflammation, from which develops (3) fibrosis with associated remodeling in the cellular microenvironment. From these changes a (4) pre-cancerous niche develops which triggers the deployment of (5) a chronic stress escape strategy, and when this fails to resolve, and (6) the transition of a normal cell to a cancer cell occurs. This paradigm provides opportunities to move away from a symptom-oriented understanding of cancer and is much closer to a cause-based understanding, which opens the door for early preventative strategies to mitigate cancer as a disease, and to interdict metastases. This is underpinned by the fact that an independent recently published proof of this paradigm showed how a stimulus trigger the proposed multi-sequence cascade of events as abrupt involution-induced chronic inflammation, followed by fibrosis with remodeling, which describes the pre-cancerous niche followed by hyperplasia, metaplasia, and cancer.
- Subjects :
- akt
aneuploidy
ap-2
bcl-2
brca
cancer
carcinogenesis
cd44
cell transition
chk2
chronic inflammation
crosstalk
disruption
dna
ecm
egfr
eicosanoid
epidemiology
epigenetics
fads2
fibrosis
genetics
genomics
glut-4
hbv
hcc
hcv
hete
homeostasis
ikk
jnk
lipid
lox
loxl2
loxl3
lta4
ltb4
ltd4
lte4
lysyl oxidase
lxa4
lxb4
mar1
mar2
metabolism
microrna
mmp
mrna
microbiome
morbid obesity
mutation
npd1
p16
p53
p120
pathogenesis
pax
pcn
pgg2
pgh2
pi3k
ppar
precancerous niche
proteomics
pufa
radiation
reproducibility
rvd1
rvd2
rvd3
rvd4
rvd5
rvd6
signaling
smt
somatic mutation theory
sox-2
spm
stat3
stem cell
targeting therapy
technology
tgf
warburg
Medicine
Science
Subjects
Details
- Language :
- English
- ISSN :
- 25570250
- Volume :
- 2
- Database :
- Directory of Open Access Journals
- Journal :
- 4 open
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.6690269480214380bb0f15776f7a247f
- Document Type :
- article
- Full Text :
- https://doi.org/10.1051/fopen/2019023