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Recent technologies and future perspectives in cancer therapies – Pubrica
Cancer is one of the
leading causes of mortality globally, and many research studies have focused in
the last decade on developing novel therapeutics to lessen the negative effects
of existing treatments. Tumors
become extremely heterogeneous as cancer progresses, resulting in a mixed
population of cells with varying molecular characteristics and therapeutic
responses.This variability may be seen at both a geographic and temporal level,
and it is a significant element in the establishment of resistance phenotypes,
which is aided by a selection pressure applied during drug administration.
Natural antioxidants in
cancer therapy:
Exogenous assaults to the human body, such
as ultraviolet (UV) rays, air pollution, and tobacco smoke, cause the creation
of reactive species, particularly oxidants and free radicals, which are
responsible for the start of many diseases, including cancer. These molecules
can be formed as a result of drug delivery in the clinic, but they can also be
formed spontaneously inside our cells and tissues by mitochondria and
peroxisomes, as well as macrophage metabolism, during normal physiological
aerobic activities.
Targeted therapy and
immunotherapy:
The
low specificity of chemotherapeutic medicines for cancer cells is one of the
key difficulties with conventional cancer treatments. In fact, most medications
have severe side effects because they act on both healthy and sick organs.
Clinical
Researchers are working hard to figure out how to
target only the targeted site. Because of their enhanced permeability and
retention effect (EPR), nanoparticles have sparked a lot of attention because
of their tendency to aggregate more in tumor tissues. The small size of
nanoparticles, as well as the leaky vasculature and poor lymphatic drainage of
neoplastic tissues, are used in this passive targeting method.
Approximately
2,900 gene therapy clinical trials are now underway, with cancer accounting for
66.6 percent of them. Different strategies are under evaluation for cancer
gene therapy: 1) targeted silencing of oncogenes, 2)
expression of pro-apoptotic and chemo-sensitising genes 3) expression of genes
able to solicit specific antitumour immune responses and 4) expression of wild
type tumour suppressor genes.
Thermal ablation and
magnetic hyperthermia:
The
term "thermal ablation of tumors" refers to a set of procedures that
use heat (hyperthermia) or cold (hypothermia) to eliminate cancerous tissues[10]. Cell necrosis is
reported to occur at temperatures as low as -40°C and as high as 60°C.. Cell
necrosis is reported to occur at temperatures as low as -40°C and as high as
60°C.
Radiomics and pathomics:
Many
clinical
research projects are focusing on the development of novel
image processing techniques in order to extrapolate information through
quantification and disease classification. To detect disease phenotypes,
flexible databases are necessary to accommodate large amounts of data from gene
expression, histology, 3D tissue reconstruction (MRI), and metabolic
characteristics (positron emission tomography, PET).
Conclusion and future
prospective
In recent years, cancer research has made
significant progress toward more effective, precise, and less intrusive cancer
treatments.While nanomedicine in combination with targeted therapy improved the
biodistribution of new or already tested chemotherapeutic agents around the
specific tissue to be treated, additional techniques, such as gene therapy,
siRNA delivery, immunotherapy, and antioxidant compounds, provide cancer
patients with new options.Thermal ablation and magnetic hyperthermia, on the
other hand, are potential alternatives to tumor resection.Finally, radiomics
and pathomics techniques aid in the handling of large data sets generated by
cancer patients in order to enhance prognosis and outcomes.
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