Biomechanical Modeling of Tumor Growth: its Relevance to Glioma Research
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@Article{IJNAMB-3-94,
author = {ANTHONY J. PALOCAREN AND CORINA S. DRAPACA},
title = {Biomechanical Modeling of Tumor Growth: its Relevance to Glioma Research},
journal = {International Journal of Numerical Analysis Modeling Series B},
year = {2012},
volume = {3},
number = {1},
pages = {94--108},
abstract = {In 2009 the US National Center for Health Statistics showed that cancer is close to becoming the deadliest disease of modern times. Recent years have seen unprecedented advancements
in medicine that have contributed to a substantial decrease in the death rates of some
serious diseases such as heart disease, stroke, influenza and pneumonia. However, with cancer,
equivalent scientific and technological advances have yet to be achieved. Theoretical models capable
of explaining the fundamental mechanisms of tumor growth and making reliable predictions
are urgently needed. These models can contribute considerably to the design of optimal, personalized
therapies that will not only maximize treatment outcomes but also reduce health care
costs. Recently [25] we have proposed a non-invasive way of classifying gliomas, primary brain
tumors, based on their stiffness. The model uses image mass spectra of proteins present in gliomas
and shows that the Young's modulus of a high grade glioma is at least 10kPa higher than the
Young's modulus of a low grade glioma. In this paper we will use this model to investigate the
effect of mechanics on the growth of gliomas. The proposed mechano-growth model is a non-linear
evolution differential equation which is solved analytically using the Adomian method. The time
evolution is represented in two ways: (1) using a classical first-order derivative, and (2) using
a fractional order derivative. Our results show that the fractional order model captures a very
interesting temporal multi-scale effect of tumor transition from low grade (benign) to high grade
(malignant) glioma when a certain threshold of mechanical strain is reached in the tissue. For
comparison, we also reproduce the results we presented in [25] when linearization is used to solve
the evolution equations analytically.},
issn = {},
doi = {https://doi.org/},
url = {http://global-sci.org/intro/article_detail/ijnamb/273.html}
}
TY - JOUR
T1 - Biomechanical Modeling of Tumor Growth: its Relevance to Glioma Research
AU - ANTHONY J. PALOCAREN AND CORINA S. DRAPACA
JO - International Journal of Numerical Analysis Modeling Series B
VL - 1
SP - 94
EP - 108
PY - 2012
DA - 2012/03
SN - 3
DO - http://doi.org/
UR - https://global-sci.org/intro/article_detail/ijnamb/273.html
KW - Tumor Mechano-Growth
KW - Adomian Method
KW - Glioma Stiffness
AB - In 2009 the US National Center for Health Statistics showed that cancer is close to becoming the deadliest disease of modern times. Recent years have seen unprecedented advancements
in medicine that have contributed to a substantial decrease in the death rates of some
serious diseases such as heart disease, stroke, influenza and pneumonia. However, with cancer,
equivalent scientific and technological advances have yet to be achieved. Theoretical models capable
of explaining the fundamental mechanisms of tumor growth and making reliable predictions
are urgently needed. These models can contribute considerably to the design of optimal, personalized
therapies that will not only maximize treatment outcomes but also reduce health care
costs. Recently [25] we have proposed a non-invasive way of classifying gliomas, primary brain
tumors, based on their stiffness. The model uses image mass spectra of proteins present in gliomas
and shows that the Young's modulus of a high grade glioma is at least 10kPa higher than the
Young's modulus of a low grade glioma. In this paper we will use this model to investigate the
effect of mechanics on the growth of gliomas. The proposed mechano-growth model is a non-linear
evolution differential equation which is solved analytically using the Adomian method. The time
evolution is represented in two ways: (1) using a classical first-order derivative, and (2) using
a fractional order derivative. Our results show that the fractional order model captures a very
interesting temporal multi-scale effect of tumor transition from low grade (benign) to high grade
(malignant) glioma when a certain threshold of mechanical strain is reached in the tissue. For
comparison, we also reproduce the results we presented in [25] when linearization is used to solve
the evolution equations analytically.
ANTHONY J. PALOCAREN AND CORINA S. DRAPACA. (2012). Biomechanical Modeling of Tumor Growth: its Relevance to Glioma Research.
International Journal of Numerical Analysis Modeling Series B. 3 (1).
94-108.
doi:
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